Trial · NCT03505099
Adverse events276
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
1 to 20 of 276
Download this page as JSON| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Lymphadenopathy | Blood and lymphatic system disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Lymphadenopathy | Blood and lymphatic system disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 0 | 15 | 0 |
| other | Microcytic anaemia | Blood and lymphatic system disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Microcytic anaemia | Blood and lymphatic system disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 2 | 15 | 3 |
| other | Thrombocytopenia | Blood and lymphatic system disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Thrombocytopenia | Blood and lymphatic system disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 0 | 15 | 0 |
| other | Iron deficiency anaemia | Blood and lymphatic system disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 0 | 14 | 0 |
| other | Iron deficiency anaemia | Blood and lymphatic system disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 1 | 15 | 1 |
| other | Dacryostenosis congenital | Congenital, familial and genetic disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Dacryostenosis congenital | Congenital, familial and genetic disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 1 | 15 | 1 |
| other | Hydrocele | Congenital, familial and genetic disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Hydrocele | Congenital, familial and genetic disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 0 | 15 | 0 |
| other | Middle ear effusion | Ear and labyrinth disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Middle ear effusion | Ear and labyrinth disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 0 | 15 | 0 |
| other | Ear pain | Ear and labyrinth disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 0 | 14 | 0 |
| other | Ear pain | Ear and labyrinth disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 1 | 15 | 2 |
| other | Precocious puberty | Endocrine disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 1 | 14 | 1 |
| other | Precocious puberty | Endocrine disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 0 | 15 | 0 |
| other | Cushingoid | Endocrine disorders | Cohort 1: Bi-allelic Deletions of SMN1 and 2 Copies of SMN2 | 0 | 14 | 0 |
| other | Cushingoid | Endocrine disorders | Cohort 2: Bi-allelic Deletions of SMN1 and 3 Copies of SMN2 | 1 | 15 | 1 |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT03505099/events