Burn
diseaseOn this page
Also known as Burn(s)
Summary
Burn (MONDO:0043519) is a disease and 503 clinical trials. Top therapeutic interventions include propranolol, mafenide, and neostigmine. A subtype of injury — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 503
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | burn |
| Mondo ID | MONDO:0043519 |
| MeSH | D002056 |
| ICD-10-CM | T20-T25 |
| NCIT | C34441 |
| SNOMED CT | 125666000 |
| Is cancer (heuristic) | no |
Also known as: Burn · burn · Burn(s)
Disease family
This is a subtype of injury. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: injury › burn
Related subtypes (9): ischemia reperfusion injury, bone fracture, acute lung injury, spinal injury, radiation injury, ankle injury, nervous system injury, frostbite, head injury
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
Drugs indicated for this disease
8 approved, 10 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Alcohol | Approved (phase 4) |
| Bacitracin | Approved (phase 4) |
| Benzocaine | Approved (phase 4) |
| Isopropyl Alcohol | Approved (phase 4) |
| Lidocaine | Approved (phase 4) |
| Menthol | Approved (phase 4) |
| Povidone-Iodine | Approved (phase 4) |
| Zinc Oxide | Approved (phase 4) |
| Ergocalciferol | Phase 3 (in late-stage trials) |
| Ibuprofen | Phase 3 (in late-stage trials) |
| Neostigmine | Phase 3 (in late-stage trials) |
| Nitrogen | Phase 3 (in late-stage trials) |
| Nitrous Oxide | Phase 3 (in late-stage trials) |
| Oxygen | Phase 3 (in late-stage trials) |
| Petrolatum | Phase 3 (in late-stage trials) |
| Stem Bromelain | Phase 3 (in late-stage trials) |
| Sugammadex | Phase 3 (in late-stage trials) |
| Tranexamic Acid | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Albumin Human, Dexmedetomidine, Fenofibrate, Heparin, Insulin Human, Itraconazole, Ketoconazole, Melatonin, Metformin, Nefopam, Nystatin, Oxandrolone, Pirfenidone, Propranolol, Ramelteon, Rosuvastatin, Silver, Silver Nitrate, Sodium Chloride, Somatropin, Sulfadiazine, Tetracycline, Thrombin, Vitamin E.
Clinical trials & evidence
Clinical trials
Clinical trials: 503.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 356 |
| PHASE2 | 34 |
| PHASE4 | 30 |
| PHASE3 | 25 |
| PHASE2/PHASE3 | 20 |
| PHASE1 | 17 |
| PHASE1/PHASE2 | 15 |
| EARLY_PHASE1 | 6 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04589442 | PHASE4 | RECRUITING | Microsurfaced Grafts in Deep Burn Wounds |
| NCT05217160 | PHASE4 | RECRUITING | Pilot Study: KeraStat® Gel for Topical Delivery of Morphine for Management of Non-Healing, Painful Open Wounds and Ulcers |
| NCT06379724 | PHASE4 | RECRUITING | Burn Study- Tranexamic Acid Versus Thrombin in Split Thickness Skin Graft |
| NCT06506565 | PHASE4 | RECRUITING | Low-Dose Ketamine Infusion During Burn Wound Care |
| NCT00149123 | PHASE4 | COMPLETED | Low-dose Hydrocortisone in Acutely Burned Patients |
| NCT00156988 | PHASE4 | COMPLETED | The Effect of Two Versus Ten Days Application of Flammacerium in Partial Thickness Burns |
| NCT00297752 | PHASE4 | COMPLETED | Treatment of Facial Burns With Flammacerium Compared to Flammazine and the Impact of Facial Burns on Psychosocial Wellbeing |
| NCT00326859 | PHASE4 | TERMINATED | Comparison of Monitored Anesthesia Care Using Remifentanil or Fentanyl for Major Dressing Changes in Burns |
| NCT00634166 | PHASE4 | TERMINATED | Effects of Therapy With Sulfamylon® 5% Topical Solution Compared to a Historical Control Group |
| NCT00860379 | PHASE4 | TERMINATED | The Effect of Selenium Supplementation Among Pediatric Patients With Burns |
| NCT01012648 | PHASE4 | UNKNOWN | Early Fluid Resuscitation With Balanced HES 130/0.4 [6%] in Severe Burn Injury |
| NCT01668030 | PHASE4 | COMPLETED | Comparison of Wound Bed Establishment in Facial Burns |
| NCT01689506 | PHASE4 | TERMINATED | Fluid Resuscitation in Patients Suffering From Burns Injury |
| NCT01926392 | PHASE4 | COMPLETED | Comparison of a Water-soluble Topical Antimicrobial to Silver Sulfadiazine in Partial Thickness Burns |
| NCT02813213 | PHASE4 | UNKNOWN | Effectiveness Comparison of Skin Micro-grafts vs Meshed Split Thickness Skin Grafts |
| NCT02952378 | PHASE4 | COMPLETED | Volume Kinetics for Hyperoncotic Albumin in Burn Patients as Well as for Healthy Subjects |
| NCT03002506 | PHASE4 | TERMINATED | Pharmacokinetics of Ceftolozane/Tazobactam in Patients With Burns |
| NCT03049930 | PHASE4 | UNKNOWN | Intraoperative Low-dose Ketamine Infusion as the Main Analgesic in Burn Patients |
| NCT03113253 | PHASE4 | COMPLETED | TRANexamic Acid to Reduce Bleeding in BURN Surgery |
| NCT03854344 | PHASE4 | COMPLETED | Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain |
| NCT03941535 | PHASE4 | UNKNOWN | Comparison of Vitamin K Doses in Patients With Larger Burn Injuries |
| NCT04152096 | PHASE4 | COMPLETED | Efficacy and Safety of Rheosorbilact® Solution for Infusion, in a Complex Therapy of Burns |
| NCT04162639 | PHASE4 | WITHDRAWN | The Relationship Between Cadaveric Allograft Skin and HLA-Sensitivity in Burn Patients |
| NCT04516148 | PHASE4 | COMPLETED | A Randomized, Controlled Trial of the Effectiveness of Perioperative Antibiotics for Reduction of Burn Wound Bacterial Concentration Following Grafting |
| NCT04681638 | PHASE4 | TERMINATED | Plasma Resuscitation Without Lung Injury |
| NCT04682782 | PHASE4 | UNKNOWN | Intraoperative Small-dose Esketamine Infusion for Pain Control in Burn Patients |
| NCT04781348 | PHASE4 | COMPLETED | Efficacy of Platelet Rich Plasma Injection Plus Fat Grafting as Compared to Fat Grafting Alone on Burn Scar by Using Vancouver Scar Scale |
| NCT05084248 | PHASE4 | COMPLETED | Vitamin D Deficiency in Adults Following a Major Burn Injury |
| NCT05465226 | PHASE4 | COMPLETED | Oliceridine in Patients With Acute Burn Injuries |
| NCT06142591 | PHASE4 | COMPLETED | Oxycodone (10, 20 mg) in a Postoperative Dressing |
| NCT06223269 | PHASE3 | RECRUITING | Safety and Efficacy of realSKIN® to Provide Complete Wound Closure of Burn Wounds as an Alternative to Autografting |
| NCT06745557 | PHASE3 | RECRUITING | Phase III Study with an Autologous Dermo-epidermal Skin Substitute for the Treatment of Burns in Adults and Adolescents |
| NCT00243243 | PHASE3 | COMPLETED | Effect of rFVIIa on Peri-operative Blood Loss in Patients Undergoing Major Burn |
| NCT00261690 | PHASE2/PHASE3 | COMPLETED | Virtual Reality Pain Control During Burn Wound Care |
| NCT00324311 | PHASE3 | COMPLETED | Enzymatic Debridement in Burns Patients: A Comparison to Standard of Care |
| NCT00426972 | PHASE3 | COMPLETED | Trial of Zesteem (Estradiol) in Healing of Split Thickness Skin Graft Donor Sites |
| NCT00539097 | PHASE2/PHASE3 | TERMINATED | Evaluation Perioperative Nutrition on Donor Site Healing in Patients Undergoing Reconstructive Burn Surg |
| NCT00548314 | PHASE3 | COMPLETED | Dermal Substitute and Topical Negative Pressure in Burns |
| NCT00591162 | PHASE2/PHASE3 | TERMINATED | Bone Disease in Severely Burned Children |
| NCT00591604 | PHASE3 | WITHDRAWN | High-Dose Vitamin D Deficiency in Burn Injury |
Drugs tested across these trials (top 30)
Related Atlas pages
- Drugs: Propranolol, Mafenide, Neostigmine, Sulfadiazine, Silver, Bacitracin, Clindamycin, Fenofibrate, Glycopyrronium, Oxandrolone, Somatropin, Albumin Human, Bupivacaine, Cefazolin, Ceftolozane, Cetirizine, Chymotrypsin, Ciprofloxacin, Collagenase Clostridium Histolyticum, Dalfampridine, Ergocalciferol, Esketamine, Estradiol, Gentamicin, Glutamine, Heparin, Hydrocortisone, HYDROXYETHYL STARCH 130/0.4, Indocyanine Green, Itraconazole