Mastocytosis Registry (of Zurich) (MastoR)

University of Zurich (UZH)

Status: Enrolling

Conditions: Mastocytosis; Hypertryptasemia

Study type: Observational

Funder types: Other

Identifiers

NCT06466889

BASEC 2020-01568

Details and patient eligibility

About

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.

Enrollment: 400 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Adult patients with mastocytsis/hypertryptasemia which are treated at the university hospital of Zurich
• available informed consent

Exclusion criteria

• denied consent

Trial design

400 participants in 2 patient groups

Mastocytosis

Description:

Diagnosed mastocytosis according to WHO criteria

Hypertryptasemia

Description:

Repeated elevated serum tryptase with no underlying mastocytosis or no bone marrow biopsy performed