The development of electrophysiological readouts for migraine attack predictio

Recruiting

• Conditions: Migraine; headache; 10019231

• Registration Number: NL-OMON55696
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 240

Inclusion Criteria

- Migraine with/ without aura or chronic migraine according to IHS /
ICHD-III-beta criteria
- Patients have to experience active migraine, which is defined for this study
as at least one migraine attack per month on average in the past 6 months.
- Age 18 years or older

Exclusion Criteria

General exclusion criteria for episodic migraine patients and healthy controls:
i) Severe depression and/or panic disorders and/or schizophrenia and/or
psychiatric disorders; ii) Epileptic disorders (epilepsy); iii) Severe visual
impairment; iv) Only for part 1: use of chronic medication (other than oral
contraceptives) in the four weeks preceding the investigation; v) Malignancy in
medical history; vi) only for part 2: use of (oral) contraceptives., Episodic
migraine patient specific: i) Only for part 1: use of prophylactic medication
for migraine in the four weeks preceding the investigation; ii) Inability to
differentiate between migraine and other variants of headache;
iii) Use of acute migraine or headache drugs on more than 6 days per month.,
Healthy control specific: i) Suffering from periodic pain attacks or a brain
disorder;
ii) Personal of family history in first-degree relatives of migraine or
trigeminal autonomic cephalgia (TAC); iii) More than one tension-type headache
in 3 months., Exclusion criteria for chronic migraine patients: i) Severe
depression and/or panic disorders and/or schizophrenia and/or psychiatric
disorders; ii) Epileptic disorders (epilepsy); iii) Severe visual impairment;
iv) Malignancy in medical history.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified