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Effect of Intranasal Oxytocin on Headache in Chronic Daily Headache - NCT00963040-02481(Clinical Trial 306542)



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City:  Wellesley Hills
State:  
MA
Zip Code: 02481
Conditions: Chronic Daily Headache
Purpose: The objective of this prospective, randomized, double-blind, parallel-group, placebo-controlled study is to determine the effectiveness of intranasal oxytocin in subjects suffering from chronic daily headache. The primary outcome measure is the reduction in headache intensity after drug administration; secondary outcome measures are the headache symptoms, nausea, vomiting, photophobia, and phonophobia. Additional secondary outcome measures are intake of rescue medication and patient satisfaction over a period of 24 hours.
Study summary:
Criteria: Inclusion Criteria: 1. Headache on equal to or more than 15 days per month for at least 6 months; the headaches can be migraine or tension. 2. More than half of the monthly headaches are of moderate or severe intensity on the 4-point categorical pain rating scale and are assessed as 6 or higher on the 11-point numerical pain rating scale. 3. Headaches typically last for at least 4 hours. 4. Subjects are on a stable headache treatment, if any, for at least 2 months. Exclusion Criteria: 1. Headache symptoms assessed to be predominately occipital. 2. Allergy to oxytocin. 3. History of addictive behavior (e.g. alcoholism, drug abuse). 4. History of significant psychiatric disorder. 5. History of clinically-significant, functionally-impairing cardiovascular or pulmonary disease. 6. Upper-respiratory tract infection at the time of randomization. 7. Past or current history of any condition that may hinder study procedures or confuse interpretation of data. 8. Nasal obstruction of any cause as determined at screening. 9. Major surgery or trauma within 4 weeks of screening. 10. Women who are pregnant as evidenced by a serum HCG, nursing, or trying to conceive. 11. Use of intranasally administered medications, for example, vasoconstrictors or corticosteroids, within 2 weeks of randomization. 12. Use of an investigational medication or device within 30 days of randomization. 13. Unable or unwilling to adhere to the study-specific procedures and restrictions. 14. Any condition that in the opinion of the investigator would compromise the safety of the subject or the quality of the data. 15. Alanine aminotransaminase (ALT) or aspartate aminotransaminase (AST) equal or greater than 3 times the upper limit of normal (ULN). 16. Serum creatinine of equal or greater than 1.8 mg/dL. Resting, sitting systolic blood pressure equal or greater than 160 mmHg or diastolic blood pressure equal or greater than 100 mmHg at screening. For patients with previously diagnosed hypertension, antihypertensive medications must be stable for at least 30 days prior to screening.
Study is available at: MedVadis Research Corporation
Wellesley Hills, MA 02481
United States

Primary Contact:
Egilius LH Spierings, MD, PhD
Email: Spierings@MedVadis.com
Phone: 781-431-1113

Secondary Contact:
Egilius LH Spierings, MD, PhD
Email: Spierings@MedVadis.com
Phone: 781-431-1113
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 23, 2011
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