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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06466889
Other study ID # BASEC 2020-01568
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 6, 2024
Est. completion date December 31, 2035

Study information

Verified date June 2024
Source University of Zurich
Contact Claudia Lang, MD
Phone +41442551111
Email claudia.lang@usz.ch
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The study aims to summarize patients with mastocytosis and hypertryptasämia (without underlying mastocytosis or no bone marrow biopsy) in relation to demographic information, clinical progress and treatment courses. Biologic samples are collected from available routine diagnostics (serum, skin tissue, gut mucosa, bone marrow, and others) for further use in experimental research.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 31, 2035
Est. primary completion date December 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Adult patients with mastocytsis/hypertryptasemia which are treated at the university hospital of Zurich - available informed consent Exclusion Criteria: - denied consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland University Hospital of Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Demographics 2010-2025
Primary Disease progression 2010-2025
See also
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