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Identification and Characterization of Genetic Variants in Hereditary Angioedema

NCT05833620 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2023-04-27

No results posted yet for this study

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

  • Hereditary Angioedema With C1 Esterase Inhibitor Deficiency

Sponsors & Collaborators

  • Hospital Universitario La Paz

    collaborator OTHER

  • Hospital Universitari Vall d'Hebron Research Institute

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-31
Primary Completion
2026-03-31
Completion
2027-03-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05833620 on ClinicalTrials.gov