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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00374530
Other study ID # KA-20060026
Secondary ID
Status Completed
Phase N/A
First received September 8, 2006
Last updated July 31, 2007
Start date August 2006

Study information

Verified date July 2007
Source Danish Headache Center
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

Before, during and after intravenous administration of PGE2 we score/measure headache, rCBF, blood flow in the middle cerebral artery and diameter of superficial temporal artery and correlate that to known pathophysiology of headache to see if PGE2 is involved in headache pathophysiology.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy volunteers

Exclusion Criteria:

- Primary Headache, headache on the day of the investigation, hypertension, hypotension, pregnant/nursing, daily intake of medication (except oral contraceptives), Cardiovascular or CNS disease, drug/alcohol abuse, psychiatric disease

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double-Blind


Related Conditions & MeSH terms


Intervention

Drug:
PGE2


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 Headache
Secondary rCBF, blood flow, diameter of STA/RA, HR, BP
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