Trials / Not Yet Recruiting
Not Yet RecruitingNCT05833620
Identification and Characterization of Genetic Variants in Hereditary Angioedema
Identification and Functional Characterization of Genetic Variants Associated With Specific Clinical Phenotypes in Hereditary Angioedema Due to C1 Inhibitor Deficiency: An Unbiased Approach
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 200 (estimated)
- Sponsor
- Hospital Universitari Vall d'Hebron Research Institute · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- —
Summary
This project aims to analyse in an unbiased way the existence of genetic variants that contribute to explaining and predicting the differences in clinical expression between patients with HAE.
Conditions
Timeline
- Start date
- 2023-05-01
- Primary completion
- 2026-03-31
- Completion
- 2027-03-31
- First posted
- 2023-04-27
- Last updated
- 2023-04-27
Locations
2 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT05833620. Inclusion in this directory is not an endorsement.