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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03152305
Other study ID # CHU-331
Secondary ID 2014-A00042-45
Status Recruiting
Phase N/A
First received May 11, 2017
Last updated May 11, 2017
Start date July 21, 2014
Est. completion date July 2018

Study information

Verified date May 2017
Source University Hospital, Clermont-Ferrand
Contact Patrick LACARIN
Phone 04 73 75 11 95
Email placarin@chu-clermontferrand.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

An increase in intracranial pressure (ICP) during migraine attacks is possible and could contribute to pain initiation and maintenance. From now on, it was not possible to measure ICP in a non-invasive way. The development of a new tool allows non-invasive self-measures of ICP variations. Thus, it is possible for the first time to look for such ICP variations during migraine attacks and to conclude if this mechanism is implied in the pathophysiology of migraine.


Description:

Womens presenting with regular menstrual migraine treated with triptans will be included in the study. Self-measure of ICP will be performed outside and during menstrual migraine attacks. The potential variations will be compared to the measures done on matched healthy women outside and during menses.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date July 2018
Est. primary completion date May 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- 18 to 50 non menopausal women

- Menstrual migraine

- Using a triptan as usual treatment to relieve attacks

- Usual triptan efficacy although recurrence is possible

Exclusion Criteria:

- Disease of the ear

- Intracranial hypertension

- Chronic daily headache

- Use of topiramate or acetazolamide

- Triptans used more than 10 days/month

- Analgesic drug used more than 15 days/month

- Uncontrolled high blood pressure

- BMI >30

- Ongoing allergic rhinitis or flu

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intracranial pressure variations
Self-measure of ICP will be performed outside and during menstrual migraine attacks.

Locations

Country Name City State
France CHU Clermont-Ferrand Clermont-Ferrand Auvergne

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intracranial pressure variations Measured during menstrual migraine attacks compared to ICP in non-migraine days and in matched healthy women during menstrual migraine attacks
Secondary Relationships between ICP variations and clinical parameters Age, BMI, pain intensity, pulsating pain, allodynia, nausea, photophobia, phonophobia, dizziness, tinnitus during menstrual migraine attacks
Secondary Relationships between ICP variations and pain relief during menstrual migraine attacks
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