Headache Inducing Characteristics and Possible Changes in Cerebral Blood Flow After Administration of PGE2
This study has been completed.
Sponsor:
Danish Headache Center
Information provided by:
Danish Headache Center
ClinicalTrials.gov Identifier:
NCT00374530
First received: September 8, 2006
Last updated: July 31, 2007
Last verified: July 2007
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
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.
| Condition | Intervention |
|---|---|
| Headache Migraine | Drug: PGE2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Double-Blind |
| Official Title: | Headache Inducing Characteristics and Possible Changes in Cerebral Blood Flow After Administration of PGE2 |
Resource links provided by NLM:
MedlinePlus related topics:
Headache
Drug Information available for:
Dinoprostone
U.S. FDA Resources
Further study details as provided by Danish Headache Center:
Eligibility| Ages Eligible for Study: | 18 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Criteria
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
Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00374530
Please refer to this study by its ClinicalTrials.gov identifier: NCT00374530
Locations
| Denmark | |
| Danish Headache Center | |
| Glostrup, Denmark, DK-2600 | |
Sponsors and Collaborators
Danish Headache Center
Investigators
| Principal Investigator: | Troels Wienecke, MD | Danish Headache Center |
More Information
| ClinicalTrials.gov Identifier: | NCT00374530 History of Changes |
| Other Study ID Numbers: |
KA-20060026 |
| Study First Received: | September 8, 2006 |
| Last Updated: | July 31, 2007 |
Additional relevant MeSH terms:
|
Headache Pain Neurologic Manifestations Nervous System Diseases Signs and Symptoms |
Dinoprostone Oxytocics Reproductive Control Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on July 18, 2017


IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. 
