IRGQ

gene
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Also known as FKSG27

Summary

IRGQ (immunity related GTPase Q, HGNC:24868) is a protein-coding gene on chromosome 19q13.31, encoding Immunity-related GTPase family Q protein (Q8WZA9). Autophagy receptor that specifically promotes clearance of misfolded MHC class I molecules by targeting them to the lysosome for degradation.

Enables protein-macromolecule adaptor activity. Involved in positive regulation of autophagy; protein quality control for misfolded or incompletely synthesized proteins; and substrate localization to autophagosome. Is active in autophagosome and lysosome.

Source: NCBI Gene 126298 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 80 total
  • MANE Select transcript: NM_001007561

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24868
Approved symbolIRGQ
Nameimmunity related GTPase Q
Location19q13.31
Locus typegene with protein product
StatusApproved
AliasesFKSG27
Ensembl geneENSG00000167378
Ensembl biotypeprotein_coding
OMIM621081
Entrez126298

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 4 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000422989, ENST00000601520, ENST00000602269, ENST00000939533, ENST00000972065

RefSeq mRNA: 2 — MANE Select: NM_001007561 NM_001007561, NM_001388309

CCDS: CCDS33040

Canonical transcript exons

ENST00000422989 — 3 exons

ExonStartEnd
ENSE000016309064358436743593367
ENSE000017040744359480943595340
ENSE000039207264359598243596134

Expression profiles

Bgee: expression breadth ubiquitous, 282 present calls, max score 93.84.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 9.3870 / max 188.2359, expressed in 1783 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1812914.43131647
1812942.11761011
1812931.7981923
1812921.0400680

Top tissues by expression

286 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
type B pancreatic cellCL:000016993.84silver quality
olfactory bulbUBERON:000226493.55gold quality
cortical plateUBERON:000534391.93gold quality
lateral nuclear group of thalamusUBERON:000273691.73gold quality
gluteal muscleUBERON:000200091.72silver quality
substantia nigra pars compactaUBERON:000196591.10gold quality
vena cavaUBERON:000408790.06gold quality
substantia nigra pars reticulataUBERON:000196689.27gold quality
ganglionic eminenceUBERON:000402389.16gold quality
dorsal root ganglionUBERON:000004488.77gold quality
Brodmann (1909) area 46UBERON:000648388.58gold quality
right hemisphere of cerebellumUBERON:001489088.56gold quality
embryoUBERON:000092288.51gold quality
lateral globus pallidusUBERON:000247688.39gold quality
dorsal plus ventral thalamusUBERON:000189788.32gold quality
cerebellar hemisphereUBERON:000224588.18gold quality
superior vestibular nucleusUBERON:000722788.13gold quality
cerebellumUBERON:000203788.08gold quality
cerebellar cortexUBERON:000212988.07gold quality
triceps brachiiUBERON:000150987.97silver quality
right frontal lobeUBERON:000281087.83gold quality
ponsUBERON:000098887.33gold quality
body of tongueUBERON:001187687.07gold quality
skeletal muscle tissue of biceps brachiiUBERON:000450287.00gold quality
adenohypophysisUBERON:000219686.82gold quality
middle temporal gyrusUBERON:000277186.71gold quality
ventral tegmental areaUBERON:000269186.62gold quality
dorsolateral prefrontal cortexUBERON:000983486.49gold quality
tracheaUBERON:000312686.41gold quality
synovial jointUBERON:000221786.32gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes4.66
E-MTAB-6075no581.75

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

281 targeting IRGQ, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-4673100.0066.641490
HSA-MIR-5692A100.0074.406850
HSA-MIR-8485100.0077.574731
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-1252-5P100.0069.802774
HSA-MIR-150-5P99.9966.691976
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-366299.9973.825684
HSA-MIR-34A-5P99.9971.211784
HSA-MIR-449A99.9971.051776
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-4645-5P99.9865.811284
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-569699.9872.364487
HSA-MIR-34C-5P99.9770.451577
HSA-MIR-449B-5P99.9770.261580
HSA-MIR-314899.9775.066478
HSA-MIR-6888-3P99.9765.951170
HSA-MIR-60799.9773.625593
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-426799.9666.532368
HSA-MIR-302E99.9670.742669
HSA-MIR-211099.9666.681930
HSA-MIR-6845-3P99.9466.881439
HSA-MIR-335-3P99.9373.364958
HSA-MIR-4760-3P99.9370.502385
HSA-MIR-498-3P99.9171.271114
HSA-MIR-6499-3P99.9066.381212

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusIrgqENSMUSG00000041037
rattus_norvegicusIrgqENSRNOG00000070901

Protein

Protein identifiers

Immunity-related GTPase family Q proteinQ8WZA9 (reviewed: Q8WZA9)

All UniProt accessions (1): Q8WZA9

UniProt curated annotations — full annotation on UniProt →

Function. Autophagy receptor that specifically promotes clearance of misfolded MHC class I molecules by targeting them to the lysosome for degradation. Acts as a molecular adapter that specifically recognizes and binds (1) misfolded MHC class I molecules following their ubiquitination, as well as (2) autophagy-related proteins, promoting the recruitment of misfolded MHC class I molecules to autophagy machinery for degradation. Degradation of misfolded MHC class I molecules is essential to prevent accumulation of defective MHC class I complexes at the surface of CD8(+) T-cells and prevent a stronger T-cell-mediated response. In contrast to other members of the family, does not show GTPase activity.

Subunit / interactions. Interacts (via LIR motif 1) with GABARAPL2. Interacts (via LIR motif 2) with MAP1LC3B/LC3B.

Subcellular location. Lysosome. Cytoplasmic vesicle. Autophagosome.

Domain organisation. The LIR motifs (LC3-interacting region) are required for the interaction with ATG8 family proteins GABARAPL2 and MAP1LC3B/LC3B.

Induction. Not induced by interferons.

Similarity. Belongs to the TRAFAC class dynamin-like GTPase superfamily. IRG family.

RefSeq proteins (2): NP_001007562, NP_001375238 (=MANE)

Domains & families (InterPro)

IDNameType
IPR030385G_IRG_domDomain
IPR040070IRGQFamily

UniProt features (25 total): helix 7, strand 6, turn 2, short sequence motif 2, chain 1, domain 1, region of interest 1, coiled-coil region 1, compositionally biased region 1, modified residue 1, disulfide bond 1, mutagenesis site 1

Structure

Experimental structures (PDB)

2 structures.

PDBMethodResolution (Å)
8Q7KX-RAY DIFFRACTION1.6
8Q6QX-RAY DIFFRACTION1.8

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8WZA9-F167.760.12

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (1): 203

Disulfide bonds (1): 152–158

Mutagenesis-validated functional residues (1):

PositionPhenotype
74abolished interaction with gabarapl2.

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 180 (showing top): GOBP_REGULATION_OF_AUTOPHAGY, GOBP_VACUOLE_ORGANIZATION, GOBP_MACROMOLECULE_CATABOLIC_PROCESS, GOBP_MACROAUTOPHAGY, WANG_LMO4_TARGETS_DN, GOBP_REGULATION_OF_CATABOLIC_PROCESS, GOBP_POSITIVE_REGULATION_OF_CATABOLIC_PROCESS, GOBP_ORGANELLE_ASSEMBLY, GOBP_POSITIVE_REGULATION_OF_AUTOPHAGY, GOBP_PROTEIN_CATABOLIC_PROCESS, GOBP_AUTOPHAGOSOME_ORGANIZATION, GOCC_AUTOPHAGOSOME, GOBP_PROTEOLYSIS, GOMF_GTPASE_ACTIVITY, GOMF_HYDROLASE_ACTIVITY_ACTING_ON_ACID_ANHYDRIDES

GO Biological Process (4): protein quality control for misfolded or incompletely synthesized proteins (GO:0006515), positive regulation of autophagy (GO:0010508), substrate localization to autophagosome (GO:0061753), autophagy (GO:0006914)

GO Molecular Function (3): protein-macromolecule adaptor activity (GO:0030674), protein binding (GO:0005515), GTP binding (GO:0005525)

GO Cellular Component (3): lysosome (GO:0005764), autophagosome (GO:0005776), cytoplasmic vesicle (GO:0031410)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein catabolic process1
autophagy1
positive regulation of catabolic process1
regulation of autophagy1
autophagosome assembly1
establishment of localization in cell1
catabolic process1
transmembrane transport1
process utilizing autophagic mechanism1
protein binding1
molecular adaptor activity1
binding1
guanyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
lytic vacuole1
vacuole1
cytoplasm1
intracellular vesicle1

Protein interactions and networks

STRING

1203 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
IRGQREPS1Q96D71562
IRGQTTC9BQ8N6N2558
IRGQAATFQ9NY61549
IRGQDMAC2Q9NW81520
IRGQCPNE1Q99829505
IRGQABRACLQ9P1F3494
IRGQTULP2O00295486
IRGQLRFN3Q9BTN0471
IRGQADPGKQ9BRR6462
IRGQOR10S1Q8NGN2444
IRGQSBK1Q52WX2433
IRGQN4BP2L2Q92802431
IRGQCORO6Q6QEF8424
IRGQZIK1Q3SY52411
IRGQIRGMA1A4Y4405

IntAct

43 interactions, top by confidence:

ABTypeScore
GABARAPL2IPO5psi-mi:“MI:0914”(association)0.690
IRGQMAP1LC3Apsi-mi:“MI:0915”(physical association)0.660
IRGQMAP1LC3Bpsi-mi:“MI:0915”(physical association)0.660
TGIF2LYPGPpsi-mi:“MI:0914”(association)0.640
OR5F1UBA6psi-mi:“MI:0914”(association)0.530
OR10H3HMGCS1psi-mi:“MI:0914”(association)0.530
NPC2NME2P1psi-mi:“MI:0914”(association)0.530
Cdk1IFT88psi-mi:“MI:0914”(association)0.350
Eea1WWP2psi-mi:“MI:0914”(association)0.350
Setd3PACSIN1psi-mi:“MI:0914”(association)0.350
ZSCAN26TDGpsi-mi:“MI:0914”(association)0.350
Tmed10NDUFS8psi-mi:“MI:0914”(association)0.350
PLK2C1orf226psi-mi:“MI:0914”(association)0.350
PRNPCARNS1psi-mi:“MI:0914”(association)0.350
SLC25A32NEDD8-MDP1psi-mi:“MI:0914”(association)0.350
NPC2NME2psi-mi:“MI:0914”(association)0.350
NFYANME2P1psi-mi:“MI:0914”(association)0.350
SCG3TPM2psi-mi:“MI:0914”(association)0.350
GABARAPL2psi-mi:“MI:0914”(association)0.350
MAPTSHTN1psi-mi:“MI:0914”(association)0.350
MED13LIGKV1-8psi-mi:“MI:0914”(association)0.350
SLC25A32AKR1A1psi-mi:“MI:0914”(association)0.350
SCG3CTHpsi-mi:“MI:0914”(association)0.350
MRPL49UBA6psi-mi:“MI:0914”(association)0.350

BioGRID (41): IRGQ (Affinity Capture-MS), IRGQ (Co-fractionation), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS), IRGQ (Affinity Capture-MS)

ESM2 similar proteins: A0A061IR73, A6H687, A6NKF1, D3KCC4, E1BD59, G3MY25, G3MZC5, O00634, O75064, P0C5W1, P20863, P27539, P52824, P54777, Q002B5, Q08DM2, Q0VCE3, Q13608, Q17RN3, Q2TBW5, Q3U0S6, Q4VYA0, Q53EQ6, Q561R2, Q568Y2, Q5BK61, Q5JR98, Q5RE82, Q5U651, Q6F5E8, Q6NY19, Q6ZS72, Q8BH83, Q8C052, Q8CDY7, Q8VIM9, Q8WZA9, Q90343, Q90ZN1, Q92985

Diamond homologs: Q8C262, Q8VIM9, Q8WZA9, Q32KW9, Q6AYF9, Q6NXR0

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 49 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Macroautophagy621.0×5e-05

GO biological processes:

GO termPartnersFoldFDR
mitophagy757.1×4e-09
autophagosome maturation654.0×1e-07
autophagosome assembly634.6×1e-06

Disease & clinical

Clinical variants and AI predictions

ClinVar

80 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance77
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

675 predictions. Top by Δscore:

VariantEffectΔscore
19:43593368:C:CCacceptor_gain1.0000
19:43594806:CA:Cdonor_loss1.0000
19:43594807:A:ACdonor_gain1.0000
19:43594807:ACCT:Adonor_gain1.0000
19:43594808:C:CAdonor_gain1.0000
19:43594808:CCT:Cdonor_gain1.0000
19:43594808:CCTC:Cdonor_gain1.0000
19:43592846:C:CAdonor_gain0.9900
19:43593363:GGAGC:Gacceptor_gain0.9900
19:43593364:GAGC:Gacceptor_gain0.9900
19:43593366:GC:Gacceptor_gain0.9900
19:43593367:CC:Cacceptor_gain0.9900
19:43593368:C:Gacceptor_loss0.9900
19:43593369:T:Aacceptor_loss0.9900
19:43594807:AC:Adonor_gain0.9900
19:43594807:ACCTC:Adonor_gain0.9900
19:43594808:CC:Cdonor_gain0.9900
19:43594808:CCTCC:Cdonor_gain0.9900
19:43595336:CATGG:Cacceptor_gain0.9900
19:43595338:TGG:Tacceptor_gain0.9900
19:43595339:GG:Gacceptor_gain0.9900
19:43595341:C:CCacceptor_gain0.9900
19:43596000:A:ACdonor_gain0.9900
19:43596001:C:CCdonor_gain0.9900
19:43592028:A:ACdonor_gain0.9800
19:43592029:C:CCdonor_gain0.9800
19:43592845:G:Adonor_gain0.9800
19:43593365:AGC:Aacceptor_gain0.9800
19:43595337:ATGG:Aacceptor_gain0.9800
19:43595350:A:Tacceptor_gain0.9800

AlphaMissense

3861 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:43592431:A:CS489R0.994
19:43592431:A:TS489R0.994
19:43592433:T:GS489R0.994
19:43593340:G:CF186L0.993
19:43593340:G:TF186L0.993
19:43593342:A:GF186L0.993
19:43595304:A:GF12S0.991
19:43592384:T:AD505V0.989
19:43592479:C:AK473N0.989
19:43592479:C:GK473N0.989
19:43592088:C:GA604P0.988
19:43595299:C:GG14R0.987
19:43595299:C:TG14R0.987
19:43592352:A:GW516R0.985
19:43592352:A:TW516R0.985
19:43592385:C:AD505Y0.985
19:43593300:C:GA200P0.984
19:43592108:G:TA597D0.983
19:43592454:A:GW482R0.982
19:43592454:A:TW482R0.982
19:43592118:A:CY594D0.981
19:43592350:C:AW516C0.981
19:43592350:C:GW516C0.981
19:43592452:C:AW482C0.981
19:43592452:C:GW482C0.981
19:43593295:A:CF201L0.981
19:43593295:A:TF201L0.981
19:43593297:A:GF201L0.981
19:43595298:C:TG14E0.981
19:43595299:C:AG14W0.981

dbSNP variants (sampled 300 via entrez): RS1000006746 (19:43584563 G>C,T), RS1000301047 (19:43596524 T>G), RS1000781750 (19:43590421 C>A,T), RS1000828208 (19:43589166 G>A), RS1000880594 (19:43588760 G>A), RS1001605966 (19:43598033 A>G), RS1001621137 (19:43591024 C>T), RS1001622941 (19:43585852 A>G), RS1002103279 (19:43584804 C>G), RS1002790807 (19:43587527 C>T), RS1003214149 (19:43593691 G>A,T), RS1003237571 (19:43585613 C>T), RS1003295581 (19:43587304 T>C), RS1004008856 (19:43586615 A>G), RS1004117278 (19:43593247 C>T)

Disease associations

OMIM: gene MIM:621081 | disease phenotypes:

GenCC curated gene-disease

Mondo (1): prostate cancer (MONDO:0008315)

Orphanet (1): Familial prostate cancer (Orphanet:1331)

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

MeSH disease descriptors (1)

DescriptorNameTree numbers
D011471Prostatic NeoplasmsC04.588.945.440.770; C12.100.500.260.750; C12.100.500.565.625; C12.200.294.260.750; C12.200.294.565.625; C12.200.758.409.750; C12.900.619.750

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

32 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases expression, increases methylation, affects expression3
Air Pollutantsaffects cotreatment, decreases expression, increases abundance, affects expression2
Leadaffects expression, decreases expression2
Ozoneaffects expression, affects cotreatment, decreases expression, increases abundance2
aristolochic acid Iincreases expression1
dicrotophosincreases expression1
triphenyl phosphateaffects expression1
alpha-pineneaffects cotreatment, decreases expression, increases abundance1
bisphenol Aincreases expression1
dimethylselenideincreases expression, increases oxidation1
sodium arseniteincreases expression1
methacrylaldehydeincreases abundance, affects cotreatment, decreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideincreases expression, affects cotreatment1
nutlin 3affects cotreatment, increases secretion1
torcetrapibincreases expression1
jinfukangaffects cotreatment, increases expression1
LDN 193189affects cotreatment, increases expression1
Sunitinibdecreases expression1
Acroleinaffects cotreatment, decreases expression, increases abundance1
Arsenicalsdecreases expression1
Cisplatinaffects cotreatment, increases expression1
Dactinomycinaffects cotreatment, increases secretion1
Doxorubicindecreases expression1
Enzyme Inhibitorsincreases O-linked glycosylation, decreases activity1
Ivermectindecreases expression1
Urethaneincreases expression1
Reactive Oxygen Speciesincreases expression, increases oxidation1
Cadmium Chloridedecreases expression1

Clinical trials (associated diseases)

300 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT00029224PHASE4COMPLETEDTreatment With Zoledronic Acid in Patients With Breast Cancer, Multiple Myeloma, and Prostate Cancer With Cancer Related Bone Lesions
NCT00035997PHASE4COMPLETEDOpen-label Trial on the Effect of I.V. Zoledronic Acid 4 mg on Bone Density in Hormone Sensitive Prostate Cancer Patients With Bone Metastasis
NCT00063609PHASE4COMPLETEDThe Effect of Zoledronic Acid on Bone Loss in Prostate Cancer Patients Undergoing Androgen Deprivation Therapy
NCT00103623PHASE4SUSPENDEDThe Plenaxis® Experience Study
NCT00106392PHASE4COMPLETEDA Safety and Efficacy Study of Prograf in the Prevention of Erectile Dysfunction After Radical Prostatectomy
NCT00185029PHASE4UNKNOWNMR-Lymphography and Lymph Node Staging in Prostate Cancer
NCT00199485PHASE4COMPLETEDAngelica Sinensis for the Treatment of Hot Flashes in Men Undergoing LHRH Therapy for Prostate Cancer
NCT00219219PHASE4COMPLETEDZoledronic Acid in the Prevention of Skeletal-related Events in Hormone Refractory and Hormone-sensitive Prostate Cancer Patients With Bone Metastases
NCT00219271PHASE4COMPLETEDEffect Of Zoledronic Acid On Circulating And Bone Marrow-Residing Prostate Cancer Cells In Patients With Clinically Localized Prostate Cancer
NCT00237146PHASE4COMPLETEDStudy to Evaluate Zoledronic Acid on Quality of Life and Skeletal-related Events as Adjuvant Treatment in Patients With Hormone-naïve Prostate Cancer and Bone Metastasis Who Have Undergone Orchiectomy
NCT00242554PHASE4COMPLETEDOpen-label Phase IV Clinical Trial to Evaluate the Safety and Tolerability of Zoledronic Acid in Patients With Prostate Cancer and Bone Metastases
NCT00280098PHASE4COMPLETEDDocetaxel in the Treatment of Hormone Refractory Prostate Cancer
NCT00293696PHASE4COMPLETEDCasodex/Zoladex Biomarkers in Localised Prostate Cancer
NCT00334139PHASE4COMPLETEDEffect of Zoledronic Acid on Bone Metabolism in Patients With Bone Metastasis and Prostate or Breast Cancer
NCT00375765PHASE4COMPLETEDEffects On Dihydrotestosterone Regulated Gene Expression In Benign Prostatic Hyperplasia Or Prostate Cancer
NCT00391690PHASE4COMPLETEDEvaluation of Bone Markers as Diagnostic Tools for Early Detection of Bone Metastases in Patients With High Risk Prostate Cancer
NCT00422708PHASE4COMPLETEDLocal Anesthesia for Prostate Biopsy
NCT00526331PHASE4COMPLETEDEvaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy
NCT00590213PHASE4COMPLETEDCompare the Value of Prophylactic Versus Therapeutic Breast Radiotherapy in CASODEX
NCT00629330PHASE4TERMINATEDDissemination of Prostate Cancer Screening to PCP’s in African American Communities
NCT00771966PHASE4COMPLETEDRadical Prostatectomy and Perioperative Fluid Therapy
NCT00805701PHASE4COMPLETEDStudy Assessing The Efficacy And Safety Of Avodart (Dutasteride) At Improving Urinary Symptoms In Men With Prostate Cancer Who Are Undergoing Seed Implantation
NCT00859027PHASE4COMPLETEDEffect Of Risedronate On Bone Mass In Older Men Receiving Neoadjuvant Therapy For Prostate Cancer
NCT00906269PHASE4UNKNOWNCan Hyperbaric Oxygen Improve Erectile Function Following Surgery for Prostate Cancer
NCT00953277PHASE4COMPLETEDStudy of Nerve Reconstruction Using AVANCE in Subjects Who Undergo Robotic Assisted Prostatectomy for Treatment of Prostate Cancer
NCT00982800PHASE4COMPLETEDDoes Postoperative Gabapentin Reduce Pain, Opioid Consumption and Anxiety and Have a Positive Effect on Health Related Quality of Life After Radical Prostatectomy?
NCT01083199PHASE4COMPLETEDGlobal Performance Evaluation of the AMS CONTINUUM™ Device
NCT01136226PHASE4COMPLETEDEvaluate Recovery of Testosterone for Patients Using Eligard
NCT01161563PHASE4COMPLETEDRandomized Crossover Trial to Assess the Tolerability of Gonadotropin Releasing Hormone (GnRH) Analogue Administration
NCT01230905PHASE4COMPLETEDStudy to Monitor the Effects of Androgen Suppression Treatment on the Heart
NCT01296672PHASE4COMPLETED3 Month Finasteride Challenge Test Can Significantly Improve the Performance of Screening for Prostate Cancer
NCT01365143PHASE4TERMINATEDProspective Randomized Trial Comparing Robotic Versus Open Radical Prostatectomy
NCT01379742PHASE4UNKNOWNComparison of Between ThinSeed™ and OncoSeed™ for Permanent Prostate Brachytherapy
NCT01486563PHASE4COMPLETEDHydroxyethyl Starch and Renal Function After Radical Prostatectomy
NCT01511874PHASE4COMPLETEDEfficacy and Safety Study of ELIGARD 22.5mg With Prostate Cancer
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