The Diameter of the Middle Cerebral Artery Measured With Magnetic Resonance Angiography

Sponsor
Danish Headache Center (Other)
Overall Status
Completed
CT.gov ID
NCT00256802
Collaborator
(none)
12
7

Study Details

Study Description

Brief Summary

To examine the ability of MRA to measure the effect of GTN on the intra-cranial vascular response during the GTN-induced headache in healthy volunteers.

Condition or Disease Intervention/Treatment Phase
  • Device: MR-angiography, GTN
N/A

Detailed Description

The only intra cranial structures innervated by sensory nerves, and therefore a possible source of the headpain are the meninges and the large intracerebral arteries. The dilatation of the cerebral vessels may not be the origin of the head pain per se, but measurements of the intra cerebral vascular bed in the past has proven valuable in the migraine-research, and has helped elucidate the basis for the migraine aura (Olesen, Friberg et al. 1990). The effects of different signal molecules on the intra cerebral vasculature continue to be an important field in the migraine research, in the search for possible pain causing signaling molecules.

Therefore we have set up at study to examine if MR-Angiography (MRA) can be used for monitoring of the vascular response after challenge with the known vasodilator GTN. This drug was chosen because it is well characterized and a large body of evidence from earlier studies could serve as background data (Thomsen 1997).

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double
Primary Purpose:
Diagnostic
Official Title:
The Diameter of the Middle Cerebral Artery Measured With Magnetic Resonance Angiography (MRA) Under Provocation With Glyceryl Trinitrate in Healthy Volunteers.
Study Start Date :
Jun 1, 2004
Study Completion Date :
Jan 1, 2005

Outcome Measures

Primary Outcome Measures

  1. The primary endpoints were the difference between the area under the curve of the MCA area and the difference between the area under the curve of the diameter of the MCA on an active day and on a placebo day recorded over 60 mins. []

Secondary Outcome Measures

  1. The secondary endpoints were difference in the area under the curve for the relative changes in area in percent deviation from baseline, and the difference in headache response. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • healthy volunteers
Exclusion Criteria:
  • history of migraine or any other type of primary headaches; any kind of daily medication (including prophylactic headache therapy but not oral contraceptives); excessive use of analgesics (corresponding to >2 g aspirin/day), pregnancy and all known contraindications for MR-examinations incl. claustrophobia.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Danish Headache Center

Investigators

  • Study Chair: Jakob Møller Hansen, MD, Danish Headache Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00256802
Other Study ID Numbers:
  • MRA-GTN2004
First Posted:
Nov 22, 2005
Last Update Posted:
Apr 1, 2009
Last Verified:
May 1, 2004
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2009