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Not Yet RecruitingNCT07218393

A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in Egypt

Retrospective and Prospective Real-World Evidence (RWE) Study Investigating Diagnosis and Therapeutic Management of Patients With HAE Type I or II in the Current Medical Practice in Egypt: the EXPLORHAE Study (EXPLORing Prospective and Retrospective Health Assessments of HAE in Egypt)

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Takeda · Industry
Sex
All
Age
1 Year
Healthy volunteers
Not accepted

Summary

Hereditary angioedema (HAE) is a rare condition. It causes sudden swelling under the skin and inside the body, like in the belly, throat, or genitals. This swelling happens because of a temporary leak in blood vessels. HAE is classified based on the amount of a protein in the blood called C1 inhibitor (C1-INH): HAE with normal C1-INH levels and HAE with limited or insufficient C1-INH levels (C1-INH deficiency); HAE with C1-INH deficiency can be divided into Type1, with low levels of C1-INH, and Type 2, in which the protein is there, but does not work properly. This study will look at people with HAE Type1 or Type2. The main aim of this study is to describe the diagnosis and management of people with HAE Type1 or HAE Type2 in Egypt. Other aims are to learn more about people with HAE Type1 or Type2, including, but not limited to, other conditions they may have, family history, impact of HAE on daily life, if treatment is stopped and the reasons. During the study, information from already existing data in a participant's medical record will be reviewed and new data will be collected during routine visits of a participant to the study clinic.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionThis is a non-interventional study.

Timeline

Start date
2026-05-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2025-10-20
Last updated
2026-03-13

Locations

7 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07218393. Inclusion in this directory is not an endorsement.