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Trigeminovascular Activation in Preventive Treatment of Headache Disorders

Trigeminovascular Activation in Preventive Treatment of Headache Disorders - TAPTHA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON50257
Enrollment
138
Registered
2020-09-21
Start date
2018-12-04
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Migraine and Cluster headache

Interventions

Capsaicin
Headache disorders
Trigeminovascular system

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Humans aged *18 years, with a history of migraine or cluster headache

Exclusion criteria

Exclusion criteria: 1. History of using neurostimulation devices within the last 2 months 2. History of botulin toxin injections in the forehead skin within the last year 3. Dermal diseases or other abnormalities on the forehead that might interfere with the measurement 4. History of sensitivity to the fruits of capsicum plants (e.g. chilli peppers) 5. Medication overuse headache 6. current use of preventive migraine/cluster headache medication. 7. Alcohol or drug abuse 6. Body mass *30kg/m2

Design outcomes

Primary

MeasureTime frame
Dermal blood flow response (Emax measured in Arbitrary Units) to capsaicin application and electrical stimulation.

Secondary

MeasureTime frame
plasma concentration of CGRP

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)