Hereditary Angioedema With C1 Esterase Inhibitor Deficiency

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Review clinical trials related to Hereditary Angioedema With C1 Esterase Inhibitor Deficiency. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Real-life Ecological Momentary Assessment of Lived Burden in Hereditary AngioEdema

The aim of this study is to conduct an in-depth analysis of the Burden of Disease (BoD) perceived by patients with Hereditary Angioedema (HAE), through daily prospective observations based on Ecological Momentary Assessment (EMA) via digital surveys and standardised questionnaires. Participants will answer online survey questions about their perceived burden of disease for 8 consecutive weeks. The main hypothesis is that daily prospective observation (EMA) will reveal a higher and more fluctuating burden of disease compared to traditional retrospective scales, providing a more accurate representation of the impact of HAE on patients' daily lives.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Istituti Clinici Scientifici Maugeri SpAUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Confirmed diagnosis of Type 1 or Type 2 hereditary angioedema; [+4]

Diagnosis of acquired angioedema or other forms of angioedema unrelated to C1-in... [+2]

Status: Not yet recruiting

Identification and Characterization of Genetic Variants in Hereditary Angioedema

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.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Hospital Universitari Vall d'Hebron Research InstituteUpdated: Apr 27, 2023Locations: 2
Eligibility criteria

Adult patients (≥ 18 years old) with HAE-C1INH diagnosis (confirmed by mutation... [+2]

No confirmed C1INH deficiency. [+2]