- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00104546
Vitamin K Injections for the Treatment of Painful Menstruation
Vitamin K Injection Treatment for Primary Dysmenorrhea: A Controlled Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Painful menstruation, also known as dysmenorrhea, is a common problem affecting a significant percentage of women. In the United States and Europe, nonsteroidal anti-inflammatory drugs (NSAIDs) and oral contraceptives are the most commonly prescribed treatments for this condition. However, in China, oral contraceptives are not commonly prescribed for unmarried women. Acu-injection, a procedure involving the injection of vitamin K into acupuncture points, has become standard treatment for dysmenorrhea at many Chinese health care facilities. This trial will assess the willingness of young Chinese women to participate in an acu-injection trial, explore the utility of pain measurements after injection, and determine the effectiveness of the injections. This study will also help in planning larger acu-injection clinical trials.
This study will last for five menstrual cycles. Participants will be randomly assigned to one of three groups. Group 1 participants will receive a vitamin K3 injection in an acupuncture point of both legs and a saline injection in the right buttock. Group 2 participants will receive a saline injection in an acupuncture point of both legs and a saline injection in the right buttock. Group 3 participants will receive a saline injection in a pseudo-acupuncture point of both legs and a vitamin K3 injection in the right buttock. Injections will be administered one time during the first 2 days of the first menstrual cycle for participants who are experiencing menstrual pain. Participants will record their level of menstrual pain before injection and at 2, 5, 30 and 60 minutes after the injections. Participants who do not respond to or are not satisfied with the acu-injection treatment will be offered either Chinese herbal medicine or NSAIDs within 1 hour of the injection. After the injection visit, participants will be asked to complete questionnaires about any menstrual pain or side effects they may be experiencing for five subsequent menstrual cycles.
Study Type
Enrollment
Phase
- Phase 1
Contacts and Locations
Study Locations
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Shanghai, China
- Menstrual Disorder Clinic of the OBS/GYN Hospital of Fudan University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Dysmenorrhea for at least 6 months prior to study entry
- Have never been pregnant or have given birth
- Mandarin Chinese or Shanghainese speaking
- Regular menstrual cycles for at least 6 months prior to diagnosis of dysmenorrhea
- Has a working home phone or cellular phone
- Willing to disclose address
- Intends to stay in the area during the study
- Parent or guardian willing to provide informed consent, if applicable
Exclusion Criteria:
- Dysmenorrhea due to any suspected or recognized causes
- Current use of hormonal contraceptives or an intrauterine device
- History of abdominal surgery
- Other concomitant therapy for acute or chronic pain
- Anticoagulant drugs
- Vitamin K acu-injections at leg acupuncture points prior to study entry
- Intolerance to NSAIDs
- Known allergy to vitamin K
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Intensity of menstrual pain before and 2, 5, 30, and 60 minutes after treatment by a 10 point Visual Analog Scale (VAS)
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presence and severity of recurrences of menstrual pain pre- and post-treatment and in 5 subsequent cycles after therapy
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Cox retrospective symptom scale
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Moos score
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Collaborators and Investigators
Investigators
- Principal Investigator: Fredi Kronenberg, PhD, Columbia University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R21AT001957 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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