Dysmenorrhea (Painful Periods) Clinical Trials

Qualified participants receive: Compensation up to $775 for time and travel related to study participation Study-related IUD at no cost Feminine hygiene products for up to 9 months Study-related medical exams at no cost   Health insurance is not required.    

Endometrial shedding during the menstrual cycle elicits profound changes in neuronal activity and cytokines producing moderate to severe pelvic pain in more than 20% of reproductive-age women. One out of every five of those women in turn will develop chronic pelvic pain (CPP), yet women without dysmenorrhea rarely report CPP. ...

As combat women soldiers are required to more intensive daily activity the investigators believe that the impact of menorrhagia, dysmenorrhea and its clinical consequence (as characterized by, anemia iron deficiency and reduced quality of life)) on personal performance will be more significant in combat women soldiers compared to non-combat women ...

The investigators propose that the sustained vaginal administration would have a better response with respect to pain, and a better safety profile than the oral administration of a non-steroidal anti-inflammatory drug. Assess the relief of the symptoms associated to dysmenorrhea a specific survey was elaborated that also included a Visual ...

Women participating in the trial will be randomly allocated to any of the three arms of the study. Treatment for 2 menstrual cycles using the PSWT Allay device (BioElectronics Corp, Frederick USA) Treatment for 2 menstrual cycles using a placebo device No treatment. If they are allocated to a device ...

The goal of this study is to see if optimized use of naproxen for treatment of dysmenorrhea will improve pain report from baseline. In addition, we will determine whether cross-organ influences from the uterus on bladder pain sensitivity change from baseline after reduced menstrual pain experience over six months. Finally, ...

5000 women diagnosed of Adenomyosis(AM) with pathology, transvaginal ultrasonography or magnetic resonance imageMRIwill be enrolled from nationwide multicenters. The investigators would build up Network platform, and database with the registered data within 6 months. 30-month follow-up with an interval of at least once every 6 months will be done for ...