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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00315666
Other study ID # 2006-000060-82
Secondary ID KA-20060021
Status Completed
Phase Phase 3
First received April 18, 2006
Last updated February 19, 2009
Start date May 2006
Est. completion date June 2007

Study information

Verified date February 2009
Source Danish Headache Center
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Interventional

Clinical Trial Summary

The purpose of this study is to test whether memantine has a prophylactic effect on chronic tension-type headaches.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date June 2007
Est. primary completion date June 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Chronic tension-type headache

- Normal urine pH

Exclusion Criteria:

- More than 1 migraine attack/month

- Other major illnesses

- Overuse of medicine/alcohol

- Women not using AC

- Pregnant/breast-feeding women

- Allergy to memantine

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
memantine


Locations

Country Name City State
Denmark Danish Headaches 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 duration
Primary Headache intensity
Secondary Headache frequency
Secondary The use of simple analgesics
Secondary Side effects
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