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Dysmenorrhea clinical trials

View clinical trials related to Dysmenorrhea.

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NCT ID: NCT01116453 Completed - Dysmenorrhea Clinical Trials

Randomized Controlled Trial of Acupuncture for Dysmenorrhea

Start date: May 2010
Phase: Phase 3
Study type: Interventional

Since there is unsatisfactory effect by currently pharmacologic therapies and preventive strategies for dysmenorrhea, this study is designed to evaluate the efficacy and quality of life of acupuncture for patients with dysmenorrhea based on the theory of traditional Chinese Medicine.

NCT ID: NCT00995917 Completed - Dysmenorrhea Clinical Trials

A Pilot Study of Acupoint Injection for Primary Dysmenorrhea

DAT
Start date: October 2009
Phase: N/A
Study type: Interventional

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: 1. Vitamin K1 acupoint injection is a safe treatment for women with menstrual pain. 2. Vitamin K1 acupoint injection reduces menstrual pain more than placebo saline injection does. 3. The treatment of vitamin K1 acupoint injection is acceptable to U.S. women. 4. Vitamin K1 is absorbed into the blood thru acupoint injection.

NCT ID: NCT00963053 Completed - Clinical trials for Primary Dysmenorrhea

VA111913 Dysmenorrhoea Efficacy and Safety Proof of Concept

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to investigate how effective VA111913 is at preventing menstrual pain in women with primary dysmenorrhoea.

NCT ID: NCT00951561 Completed - Dysmenorrhea Clinical Trials

A Comparison Study of Pain Relief From Dysmenorrhea Between the Vipon Tampon and Ibuprofen

Start date: November 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the Vipon tampon with ibuprofen in relieving pain in women with dysmenorrhea. Subjects completed a total of 4 treatment intervals; each subject was randomized to use the VIPON as their treatment for two intervals and Ibuprofen as their treatment for two intervals.

NCT ID: NCT00909857 Completed - Clinical trials for Primary Dysmenorrhea

Effect on Primary Dysmenorrhea

Start date: April 2009
Phase: Phase 3
Study type: Interventional

To investigate the potential benefits of a new oral contraceptive (SH T00658ID) on alleviating complaints of dysmenorrhea associated with oral contraceptive use.

NCT ID: NCT00902746 Completed - Dysmenorrhea Clinical Trials

Efficacy and Safety, Long-Term Study of NPC-01 to Treat Dysmenorrhea Associated With Endometriosis

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The purpose of this long-term study is to determine whether NPC-01 is effective in the treatment of dysmenorrhea associated with endometriosis.

NCT ID: NCT00855829 Completed - Dysmenorrhea Clinical Trials

A Feasibility Study Designed to Assess the Efficacy of the ActiLady Device in Adult Female Subjects With Dysmenorrhea

Start date: May 2010
Phase: Phase 1
Study type: Interventional

ActiLady refers is employing targeted pressure waves, with the goal of reducing the pain associated with menstruation (clinically known as dysmenorrhea).

NCT ID: NCT00769964 Completed - Dysmenorrhea Clinical Trials

VA111913 TS: First in Human Study

Start date: September 2008
Phase: Phase 1
Study type: Interventional

This is a first-in-human study of VA111913 TS, a new chemical entity being developed for the treatment of dysmenorrhea. This study is designed to investigate determine the safety, tolerability and pharmacokinetics of VA111913 TS after single and multiple doses in healthy non-pregnant female volunteers of child bearing age.

NCT ID: NCT00746096 Completed - Dysmenorrhea Clinical Trials

Efficacy and Safety Study of Low Dose Oral Contraceptive Pill to Treat Primary Dysmenorrhea

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether combination oral contraceptive pill of norethindrone and ethinyl estradiol is effective in the treatment of primary dysmenorrhea.

NCT ID: NCT00651313 Completed - Dysmenorrhea Clinical Trials

Efficacy and Safety Study of Lidocaine Vaginal Gel for Recurrent Dysmenorrhea (Painful Periods)

Lidocaine 04
Start date: August 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether lidocaine vaginal gel is safe and effective for preventing or reducing the severity of dysmenorrhea (painful menstrual periods) compared to placebo (inactive gel).