Tetanus
diseaseOn this page
Also known as Clostridium tetani caused infectious disease of the nervous systemClostridium tetani infectious disease of the nervous systemlockjaw
Summary
Tetanus (MONDO:0005526) is a disease and 236 clinical trials. Top therapeutic interventions include streptococcus pneumoniae polysaccharide conjugated to corynebacterium diphtheriae crm197, rotavirus, live attenuated, and tetanus toxoid. A subtype of primary bacterial infectious disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Europe) [Orphanet-validated]
- Phenotypes (HPO): 30
- Clinical trials: 236
Clinical features
Epidemiology
Prevalence records
23 prevalence record(s), Orphanet, top 20 (validated / broadest geography first):
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | 0.024 | Europe | Validated |
| Annual incidence | <1 / 1 000 000 | 0.014 | France | Validated |
| Annual incidence | <1 / 1 000 000 | 0.044 | Malta | Validated |
| Annual incidence | <1 / 1 000 000 | 0.01 | Slovakia | Validated |
| Annual incidence | <1 / 1 000 000 | 0.014 | Bulgaria | Validated |
| Annual incidence | <1 / 1 000 000 | 0.028 | Croatia | Validated |
| Annual incidence | <1 / 1 000 000 | 0.004 | Czech Republic | Validated |
| Annual incidence | <1 / 1 000 000 | 0.014 | Denmark | Validated |
| Annual incidence | <1 / 1 000 000 | 0.032 | Estonia | Validated |
| Annual incidence | <1 / 1 000 000 | 0.036 | Greece | Validated |
| Annual incidence | <1 / 1 000 000 | 0.024 | Hungary | Validated |
| Annual incidence | <1 / 1 000 000 | 0.016 | Ireland | Validated |
| Annual incidence | <1 / 1 000 000 | 0.076 | Italy | Validated |
| Annual incidence | <1 / 1 000 000 | 0.07 | Lithuania | Validated |
| Annual incidence | <1 / 1 000 000 | 0.008 | Netherlands | Validated |
| Annual incidence | <1 / 1 000 000 | 0.012 | Norway | Validated |
| Annual incidence | <1 / 1 000 000 | 0.032 | Poland | Validated |
| Annual incidence | <1 / 1 000 000 | 0.008 | Portugal | Validated |
| Annual incidence | <1 / 1 000 000 | 0.032 | Romania | Validated |
| Annual incidence | 1-9 / 1 000 000 | 0.118 | Slovenia | Validated |
Signs & symptoms
Clinical features (HPO)
30 HPO clinical features (Orphanet curated; top 30 by frequency):
| HPO ID | Term | Frequency |
|---|---|---|
| HP:0000211 | Trismus | Very frequent (80-99%) |
| HP:0002015 | Dysphagia | Very frequent (80-99%) |
| HP:0002179 | Opisthotonus | Very frequent (80-99%) |
| HP:0003552 | Muscle stiffness | Very frequent (80-99%) |
| HP:0040212 | Risus sardonicus | Very frequent (80-99%) |
| HP:0001276 | Hypertonia | Frequent (30-79%) |
| HP:0001649 | Tachycardia | Frequent (30-79%) |
| HP:0001945 | Fever | Frequent (30-79%) |
| HP:0002063 | Rigidity | Frequent (30-79%) |
| HP:0005363 | Humoral immunodeficiency | Frequent (30-79%) |
| HP:0011355 | Localized skin lesion | Frequent (30-79%) |
| HP:0011964 | Intermittent painful muscle spasms | Frequent (30-79%) |
| HP:0025258 | Stiff neck | Frequent (30-79%) |
| HP:0000822 | Hypertension | Occasional (5-29%) |
| HP:0001259 | Coma | Occasional (5-29%) |
| HP:0001337 | Tremor | Occasional (5-29%) |
| HP:0001662 | Bradycardia | Occasional (5-29%) |
| HP:0002027 | Abdominal pain | Occasional (5-29%) |
| HP:0002098 | Respiratory distress | Occasional (5-29%) |
| HP:0002501 | Spasticity of pharyngeal muscles | Occasional (5-29%) |
| HP:0002607 | Bowel incontinence | Occasional (5-29%) |
| HP:0002789 | Tachypnea | Occasional (5-29%) |
| HP:0003236 | Elevated circulating creatine kinase concentration | Occasional (5-29%) |
| HP:0003345 | Elevated urinary norepinephrine | Occasional (5-29%) |
| HP:0003639 | Elevated urinary epinephrine | Occasional (5-29%) |
| HP:0005341 | Autonomic bladder dysfunction | Occasional (5-29%) |
| HP:0006824 | Cranial nerve paralysis | Occasional (5-29%) |
| HP:0012332 | Abnormal autonomic nervous system physiology | Occasional (5-29%) |
| HP:0025145 | Rigors | Occasional (5-29%) |
| HP:0025425 | Laryngospasm | Occasional (5-29%) |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | tetanus |
| Mondo ID | MONDO:0005526 |
| EFO | EFO:0005593 |
| MeSH | D013742 |
| Orphanet | 3299 |
| DOID | DOID:11338 |
| ICD-11 | 1793762788 |
| NCIT | C85185 |
| SNOMED CT | 276202003, 76902006 |
| UMLS | C0039614 |
| MedGen | 21489 |
| GARD | 0005144 |
| MedDRA | 10043376 |
| Is cancer (heuristic) | no |
Also known as: Clostridium tetani caused infectious disease of the nervous system · Clostridium tetani infectious disease of the nervous system · lockjaw
Disease family
This is a subtype of primary bacterial infectious disease. 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: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious disease › bacterial infectious disease › primary bacterial infectious disease › tetanus
Related subtypes (36): Buruli ulcer disease, sennetsu fever, salmonellosis, pinta disease, chancroid, gonorrhea, anthrax infection, leprosy, botulism, diphtheria, bartonellosis, brucellosis, campylobacteriosis, glanders, granuloma inguinale, legionellosis, leptospirosis, listeriosis, Mycobacterium avium complex disease, ornithosis, rhinoscleroma, staphyloenterotoxemia, syphilis, cholera, ehrlichiosis, melioidosis, tuberculosis, tularemia, plague, Q fever, shigellosis, Lyme disease, relapsing fever, spirillary rat-bite fever, streptobacillary rat-bite fever, Borrelia miyamotoi disease
Subtypes (1): tetanus neonatorum
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
3 approved, 2 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Diphtheria Toxoid | Approved (phase 4) |
| Hepatitis B Virus Hbsag Surface Protein Antigen | Approved (phase 4) |
| Tetanus Toxoid | Approved (phase 4) |
| Pertussis Vaccine | Phase 3 (in late-stage trials) |
| Siltartoxatug | Phase 3 (in late-stage trials) |
Clinical trials & evidence
Clinical trials
Clinical trials: 236.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| PHASE3 | 106 |
| PHASE4 | 47 |
| Not specified | 33 |
| PHASE2 | 25 |
| PHASE1 | 13 |
| PHASE1/PHASE2 | 7 |
| PHASE2/PHASE3 | 5 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00168545 | PHASE4 | COMPLETED | Immunology of Non-specific Effects of Vaccine |
| NCT00254917 | PHASE4 | COMPLETED | Assessment of the Immunogenicity and Safety of PENTAXIM™ in Philippines |
| NCT00255021 | PHASE4 | COMPLETED | Immunogenicity and Safety of Sanofi Pasteur Pentaxim Combined Vaccine in Infants in Thailand |
| NCT00282295 | PHASE4 | COMPLETED | US-licensed Combined Vaccine Against Tetanus & Diphtheria, Given With US-licensed Vaccine Against Meningococcal Disease |
| NCT00304265 | PHASE4 | COMPLETED | Post-marketing Evaluation of Reactions Following Receipt of Recommended Adolescent Pertussis Vaccine |
| NCT00319553 | PHASE4 | COMPLETED | Post-licensure, Modified Double-blind, Multi-center Study Evaluating Safety and Immunogenicity of ADACEL® and BOOSTRIX® |
| NCT00325156 | PHASE4 | COMPLETED | Assess the Safety & Reactogenicity of DTPa-IPV/Hib Vaccine Administered at 3, 4, 5 & 18 Mths of Age, in Healthy Infants |
| NCT00347958 | PHASE4 | COMPLETED | Descriptive, Open-label, Multicenter Study of the Safety of Redosing With ADACEL® Vaccine |
| NCT00437671 | PHASE4 | TERMINATED | Tetanus Immunization in Subjects With No Immunization History or With Tetanus Antibody Levels Below Protective Levels |
| NCT00457249 | PHASE4 | COMPLETED | A Trial to Evaluate the Safety and Immunogenicity of ADACEL® Vaccine in Persons 65 Years of Age and Older |
| NCT00514059 | PHASE4 | COMPLETED | Immunogenicity and Safety Study of a Booster Dose (5th) of Diphteria-Tetanus-Pertussis-Polio Vaccine |
| NCT00544271 | PHASE4 | TERMINATED | Immunogenicity, Antibody Persistence and Safety of GSK Biologicals’ DTPa (INFANRIX) and dTpa (BOOSTRIX) Vaccines. |
| NCT00548171 | PHASE4 | COMPLETED | Immunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination in Study NCT01267058 |
| NCT00601835 | PHASE4 | COMPLETED | Canadian Manufactured Tetanus and Diphtheria Toxoids Adsorbed (Td) Vaccine Compared With U.S. Manufactured Td |
| NCT00610168 | PHASE4 | COMPLETED | Immunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination. |
| NCT00611559 | PHASE4 | COMPLETED | Study of a New Formulation of DTPa-HBV-IPV/Hib Vaccine Administered as a Booster Dose to 18-23 Months Old Children |
| NCT00617812 | PHASE4 | COMPLETED | Safety and Immunogenicity Study of a Liquid Pentavalent Combination Vaccine |
| NCT00635128 | PHASE4 | COMPLETED | Safety and Immunogenicity of a Booster Dose of GSK Biological’s Boostrix-Polio Vaccine |
| NCT00674908 | PHASE4 | COMPLETED | Phase IV Interchangeability Study of a Liquid Pentavalent Combination Vaccine |
| NCT00712959 | PHASE4 | COMPLETED | Immune Responses in Adults to Revaccination With ADACEL® 10 Years After a Previous Dose |
| NCT00753649 | PHASE4 | COMPLETED | Immunogenicity and Safety of GSK Biologicals’ Infanrix Hexa in Infants |
| NCT00777257 | PHASE4 | COMPLETED | Study of Menactra® in US Adolescents When Administered Concomitantly With Tdap Vaccine |
| NCT00802867 | PHASE4 | COMPLETED | Study of DAPTACEL® Administered as a 5th Dose in 4 to 6-Year-Old Children Previously Immunized With PENTACEL™ |
| NCT00870350 | PHASE4 | UNKNOWN | An Immunogenicity and Safety Study of Tetanus, Diphtheria and Acellular Pertussis Vaccine Booster |
| NCT00877357 | PHASE4 | UNKNOWN | Safety, Long Term Immunogenicity and Lot Consistency Study of Liquid Pentavalent Combination Vaccine |
| NCT01031303 | PHASE4 | COMPLETED | Immunogenicity and Safety of TETRAXIM™ Given as a Booster Dose at 4 to 6 Years of Age |
| NCT01137435 | PHASE4 | COMPLETED | Post Marketing Surveillance for ADACEL™ in South Korea |
| NCT01147900 | PHASE4 | COMPLETED | Evaluation of Boostrix™10 Years After Previous Booster Vaccination |
| NCT01294605 | PHASE4 | COMPLETED | Immunogenicity and Reactogenicity Study of BoostrixTM (dTpa) and Boostrix-IPV (dTpa-IPV) |
| NCT01311557 | PHASE4 | COMPLETED | Study of Adacel® Vaccine Administered to Persons 10 Years of Age |
| NCT01323959 | PHASE4 | COMPLETED | Immunogenicity and Safety of Booster Dose of BoostrixTM Polio Vaccine in Previously Boosted Adults |
| NCT01357720 | PHASE4 | COMPLETED | Study to Assess if Quinvaxem Can be Interchanged With Other Pentavalent Vaccines During Standard Childhood Vaccination |
| NCT01358825 | PHASE4 | COMPLETED | Study to Evaluate Antibody Persistence in Children Previously Vaccinated With Infanrix Hexa™ or Infanrix-IPV/Hib™ |
| NCT01362322 | PHASE4 | COMPLETED | Immunogenicity and Safety of BoostrixTM Using a New Syringe in 10 to 15-year Old Adolescents |
| NCT01437423 | PHASE4 | COMPLETED | Regulatory Post-Marketing Surveillance Study for TETRAXIM™ |
| NCT01439165 | PHASE4 | COMPLETED | Safety and Immunogenicity in Adults of Revaccination With Adacel® Vaccine 10 Years After a Previous Dose |
| NCT01457547 | PHASE4 | COMPLETED | Comparison of Immunogenicity and Reactogenicity of INFANRIX™ HEXA and HEXAVAC™ Vaccines as a Primary Vaccination Course |
| NCT01491087 | PHASE4 | COMPLETED | Safety of PENTAXIM® Given as a Three-Dose Primary Vaccination at 2, 3, and 4 Months of Age in Infants in China |
| NCT01546909 | PHASE4 | COMPLETED | Antibody Persistence to REVAXIS or DT Polio and Immune Response to TETRAVAC-ACELLULAIRE |
| NCT01629589 | PHASE4 | COMPLETED | Immunogenicity of Adacel® and BOOSTRIX® Vaccines in Adolescents |
Drugs tested across these trials (top 30)
Related Atlas pages
- Drugs: STREPTOCOCCUS PNEUMONIAE POLYSACCHARIDE CONJUGATED TO CORYNEBACTERIUM DIPHTHERIAE CRM197, Rotavirus, Live Attenuated, Tetanus Toxoid, Hepatitis B Virus Hbsag Surface Protein Antigen, Pentetic Acid, Sodium Chloride, TECHNETIUM TC 99M PENTETATE, HAEMOPHILUS INFLUENZAE TYPE B STRAIN 20752 CAPSULAR POLYSACCHARIDE TETANUS TOXOID CONJUGATE ANTIGEN, Siltartoxatug, Pertussis Vaccine