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Assessment of somatosensory profiles using quantitative sensory testing (QST) in patients with mast cell activation disease (MCAD)

Assessment of somatosensory profiles using quantitative sensory testing (QST) in patients with mast cell activation disease (MCAD)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00029122
Enrollment
80
Registered
2022-06-17
Start date
2026-07-17
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mast cell activation syndrome (MCAS

Interventions

Group 1: Patients with a diagnosis of mast cell activation disease (MCAD): A one-time quantitative sensory testing (QST) assessment will be performed, together with the collection of clinical and life

Sponsors

Universitätsklinikum Bonn
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: • Confirmed diagnosis of a mast cell activation disease (MCAD): - Mastocytosis according to the World Health Organization (WHO) diagnostic criteria - Mast cell activation syndrome (MCAS) according to the diagnostic criteria proposed by Afrin, Molderings et al. (2020) • Prior provision of study information and written informed consent

Exclusion criteria

Exclusion criteria: • Inability to provide written informed consent • Inability to follow the verbal instructions required for quantitative sensory testing (QST) • Regular use of analgesics, psychotropic medication, or other medications that may affect pain perception within the previous 4 weeks • Contraindications to quantitative sensory testing (QST): skin and soft tissue disorders, pregnancy, or breastfeeding

Design outcomes

Primary

MeasureTime frame
Differences in somatosensory profiles between patients with mast cell activation disease (MCAD) and healthy controls, assessed by a single quantitative sensory testing (QST) procedure.

Secondary

MeasureTime frame
Association between individual quantitative sensory testing (QST) parameters and clinical characteristics and medical history of patients, as assessed by questionnaire.

Countries

Germany

Contacts

Public ContactRumeysa Polat

Universitätsklinikum Bonn

rumeysa.polat@uni-bonn.de0049 176 74832118

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026