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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03560024
Other study ID # H-18016693
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 31, 2018
Est. completion date December 31, 2018

Study information

Verified date February 2019
Source Danish Headache Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Studying Pituitary adenylate cyclase-activating peptide 27 (PACAP27) effects on extra- and intracerebral arteries assessed by MRA on healthy volunteers.


Description:

PACAP neuropeptide, which belongs to the vasoactive intestinal polypeptide (VIP)/glucagon/secretin family. PACAP exists in two forms: Studying Pituitary adenylate cyclase-activating peptide 38 (PACAP38), which consists of 38 amino acids and PACAP27 which contains 27 amino acids at its N-terminus. PACAP38 is implicated in migraine pathophysiology however PACAP27 is not studied well. Therefore, the investigators will study PACAP27's effect on extra- and intracerebral arteries assessed by MRA on healthy volunteers.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
PACAP27
PACAP27 is vasodilator of cerebral vessels
Placebo
Saline

Locations

Country Name City State
Denmark Danish Headache Center Glostrup

Sponsors (1)

Lead Sponsor Collaborator
Danish Headache Center

Country where clinical trial is conducted

Denmark, 

Outcome

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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