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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00510172
Other study ID # KA-20060086
Secondary ID
Status Recruiting
Phase N/A
First received July 30, 2007
Last updated July 30, 2007
Start date December 2006
Est. completion date September 2007

Study information

Verified date July 2007
Source Glostrup University Hospital, Copenhagen
Contact Troels Wienecke, MD
Phone + 45 43 23 45 14
Email trowie01@glo.regionh.dk
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

We hypothesised that intravenous infusion of PGI2 induced headache or migraine and cranial vasodilatation in migraineurs.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date September 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- migraine without aura and healthy apart from that

- age 18-55 years

- 50-100 kg

- Secure contraceptives

Exclusion Criteria:

- Tension Type Headache more than 3 time a month

- Other primary headaches

- Medication prior to the study (closer than 4 times plasma halflife)

- Migraine or headache 5 days prior to study.

- Hypertension (systolic BP >150 mmHg and/or diastolic BP >100 mmHg).

- Hypotension (systolic BP <90 mmHg and/or diastolic BP <50 mmHg).

- Heart-vessel disease of any kind incl cerebrovascular disease.

- Anamnestic or clinical signs of psychiatric disease or abuse.

- Anamnestic or clinical signs of disease of any kind relevant for participation in the study.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
Prostacyclin, PGI2
10 ng/kg/min of epoprostenol (stable PGI2)
Placebo
NaCL 0,9%

Locations

Country Name City State
Denmark Danish Headache Center Copenhagen Glostrup

Sponsors (1)

Lead Sponsor Collaborator
Glostrup University Hospital, Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Headache and accompanying symptoms. Blood flow velocity in the middle cerebral artery, diameter changes in superficial temporal artery and radial artery. 14 hours
Secondary Blood pressure, pulse 100 min
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