Space motion sickness
diseaseOn this page
Also known as adaptation syndrome, Spacemotion sickness, SpaceSpace adaptation syndromesyndrome, Space adaptation
Summary
Space motion sickness (MONDO:0003147) is a disease and 5 clinical trials. Top therapeutic interventions include promethazine. A subtype of motion sickness — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 5
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | space motion sickness |
| Mondo ID | MONDO:0003147 |
| MeSH | D018489 |
| DOID | DOID:4796 |
| UMLS | C0242700 |
| MedGen | 116642 |
| GARD | 0023385 |
| Is cancer (heuristic) | no |
Also known as: adaptation syndrome, Space · motion sickness, Space · Space adaptation syndrome · syndrome, Space adaptation
Disease family
This is a subtype of motion sickness. 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 body system or component › auditory system disorder › inner ear disorder › motion sickness › space motion sickness
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
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 5.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
| PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05852730 | PHASE2 | RECRUITING | Combination of Intranasal Scopolamine and Sensory Augmentation to Mitigate G-transition Induced Motion Sickness and Enhance Sensorimotor Performance |
| NCT05886660 | PHASE2 | RECRUITING | Combination of Intranasal Scopolamine and Sensory Augmentation to Mitigate G-transition Induced Motion Sickness and Enhance Sensorimotor Performance |
| NCT05622344 | Not specified | RECRUITING | StableEyes With Active Neurofeedback |
| NCT06431984 | Not specified | COMPLETED | Pharmacology Space Kit (PSK) - Dried Blood Spot for Caffeine Pharmacokinetics Under Microgravity Conditions |
| NCT07318142 | Not specified | COMPLETED | Virtual Reality in the Rehabilitation of Visually Induced Motion Sickness |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| PROMETHAZINE | 4 | 1 |
Related Atlas pages
- Drugs: Promethazine