A Pilot Study of Acupoint Injection for Primary Dysmenorrhea (DAT)
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|ClinicalTrials.gov Identifier: NCT00995917|
Recruitment Status : Completed
First Posted : October 16, 2009
Last Update Posted : April 20, 2012
Many women, particularly adolescent women, suffer from painful menstrual cramps, medically referred to as dysmenorrhea. Common treatments for menstrual cramps are non-steroidal anti-inflammatory drugs and oral contraceptives, but both have side effects that limit their use. Injection of vitamin K into an acupuncture point has been used as treatment for dysmenorrhea at the Obstetrics & Gynecology Hospital in Shanghai, China since at least 1985. More research is needed on the effectiveness of this treatment and its acceptability to different women. The objective of this study is to examine the feasibility and effectiveness of acupoint injection of vitamin K1 for the treatment of severe primary dysmenorrhea in the United States. Twenty participants will be randomized to receive either 1) vitamin K1 injection into an acupuncture point at the start of their menstrual cycle followed by a saline injection in a non-acupuncture point two months later or 2) saline injection in a non-acupuncture point followed by vitamin K1 injection into an acupuncture point two months later. The primary outcome measure will be change in pain intensity measured before and after each treatment. Data on other menstrual symptoms will be collected by telephone or a web-based survey. Three additional participants will be recruited to receive vitamin K1 injection into an acupuncture point and have blood samples drawn before and after injection to determine absorption of vitamin K1. The aims of the study are to collect preliminary data on the efficacy and safety of vitamin K1 injected in an acupoint for the treatment of severe primary dysmenorrhea; assess the feasibility and acceptability of the treatment among U.S. women; and test the blood absorption of vitamin K1 following acupoint injection treatment.
The investigators hypothesize that:
- Vitamin K1 acupoint injection is a safe treatment for women with menstrual pain.
- Vitamin K1 acupoint injection reduces menstrual pain more than placebo saline injection does.
- The treatment of vitamin K1 acupoint injection is acceptable to U.S. women.
- Vitamin K1 is absorbed into the blood thru acupoint injection.
|Condition or disease||Intervention/treatment||Phase|
|Dysmenorrhea Pain, Menstrual||Other: Vitamin K acupoint injection Other: Saline Injection||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||18 participants|
|Intervention Model:||Crossover Assignment|
|Official Title:||A Randomized, Crossover, Pilot Trial of the Feasibility and Safety of Acupoint Injection of Vitamin K for Treatment of Primary Dysmenorrhea|
|Study Start Date :||October 2009|
|Actual Primary Completion Date :||June 2011|
|Actual Study Completion Date :||July 2011|
Experimental: Vitamin K acupoint injection
Participants will receive the vitamin K intervention within 2 days of the onset of painful menstrual cramps.
Other: Vitamin K acupoint injection
Vitamin K will be injected into an acupuncture point within 2 days of the onset of painful menstrual cramps. Injections of 5 mg/0.5ml of vitamin K1 will be administered in bilateral acupuncture points. A single shot of vitamin K1 is 10mg/ml. Five mg/0.5ml will be drawn twice from one ampule and injected into each bilateral site, for a total dose of 10mg/ml of vitamin K.
Sham Comparator: Saline Injection
Participants will receive the saline treatment within 2 days of the onset of painful menstrual cramps.
Other: Saline Injection
Injection of .5ml saline bilaterally into both legs within 2 days of the onset of painful menstrual cramps.
- self-reported pain [ Time Frame: 3-5 months ]
- medications used during menstrual cycle [ Time Frame: 3-5 months ]
- activity restriction [ Time Frame: 3-5 months ]
- vitamin K content in blood [ Time Frame: 1-2 months ]
- Cox retrospective symptom scale [ Time Frame: 3-5 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00995917
|United States, California|
|Mount Zion Outpatient Unit|
|San Francisco, California, United States, 94115|
|Principal Investigator:||Maria Chao, Dr PH, MPA||University of California, San Francisco|