Headache, Migraine Clinical Trial
Official title:
The Effect of PACAP27 on the Extra- and Intracerebral Arteries Assessed by MRA on Healthy Volunteers
Verified date | February 2019 |
Source | Danish Headache Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Studying Pituitary adenylate cyclase-activating peptide 27 (PACAP27) effects on extra- and intracerebral arteries assessed by MRA on healthy volunteers.
Status | Completed |
Enrollment | 18 |
Est. completion date | December 31, 2018 |
Est. primary completion date | December 31, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Healthy volunteers - Aged 18-50 - 50-100 kg Exclusion Criteria: - Tension type headache more than 5 dag /month - Other primary headaches - Daily medication except contraceptives - Drug taken within 4 times the half-life for the specific drug except contraceptives - Pregnant or lactating women - Exposure to radiation within the last year - Headache within the last 24 hours before start of trial - Hypertension - Hypotension - Respiratory or cardiac disease - Primary relatives with current or previous migraine |
Country | Name | City | State |
---|---|---|---|
Denmark | Danish Headache Center | Glostrup |
Lead Sponsor | Collaborator |
---|---|
Danish Headache Center |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Dilation of extra- and intracerebral arteries | A single-slab 3D time-of-flight (3D TOF) MRA of extra- and intracranial arteries will be acquired as described in previous studies (Amin et al., 2013, 2014). MRA data will be analyzed by LKEB-MRA vessel wall analysis software program. We will measure the circumference of vessels in millimeter in five predefined time points (0, 20, 110, 200 and 290 min) | 0-290 min | |
Secondary | Headache | Headache intensity (Visual analog scale 0-10), characteristics, location and migraine associated symptoms will be recorded in questionnaire at hospital (6 hours) and post hospital (18 hours). In hospital phase, headache questionnaire will be filled every 30 min and post hospital every hour. | 0 to 24 hours |
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