Found 71 Menstruation trials
A listing of Menstruation medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
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This study involves 4 study visits over the course of 2 months. You will be asked to track your menstrual cycle (if applicable) and will come in for 3 sessions of TMS and blood draws. Compensation is incremental and corresponds to study participation. Total compensation for the study is $500.FILL …
Please see section 3.0 of the attached protocol Please see the attached protocol Please see the attached protocol
The purpose of this research study is to better understand anxiety fluctuations during the perinatal period using technology-based daily assessment of mood, anxiety, sleep, and activity levels. This study uses a daily mood diary to monitor anxiety and wearable technology to track sleep and physical activity. All tasks during the 28-day …
POWERS (Physiology of the Weight Reduced State) is a national research study funded by the NIH. The study involves a behavioral weight loss intervention, a weight-stable period, and an observational phase. Participants will monitor their weight at home with an internet-connected scale and come to Penn Medicine for two screening …
The Women's Health Clinical Research Center at Penn Medicine is conducting a paid research study to see if women with sickle cell disease (SCD) experience any pain differences while using the birth control injection known as Depo, as compared to when not using it. Depo-Provera is already FDA-approved, safe to …
The purpose of this study is to evaluate the safety and efficacy of using multiple medicines compared to a single medicine in subjects with moderate to severe Crohn's Disease. Each group will have a 35-day screening period, followed by a 12-week induction period, a 12-week maintenance period, and a follow-up …
This study investigates progressive CLAD in individuals who have undergone bilateral lung transplantation. The purpose of this study is to evaluate the safety and effectiveness of an investigational medication in comparison to a placebo.The study focuses on assessing how well the investigational medication works and its safety in patients who …
This is a phase III, double-blind, placebo-controlled study to evaluate the efficacy and safety or NI0752 in participants with Progressive Supranuclear Palsy (PSP). Participants will receive either 50mg of NI0752 or placebo every 12 weeks for 72 weeks via intrathecal injection during the double-blind period followed by an OLE period.
The purpose of this study is to evaluate the efficacy and safety of concomitant use of eplontersen and ALXN2220 compared with eplontersen and placebo in adult participants with ATTR-CM who are treated with standard-of-care therapy as determined by the treating and study physician(s). The study duration will be up to …
The study evaluates the efficacy and safety of brenipatide vs. placebo as an add-on to ongoing MDD treatment. Eligible participants have MDD in remission or near remission with residual symptoms. They will complete a ~4-week Screening period before randomization, followed by a Double-Blind Adjunctive Treatment period until relapse, other discontinuation …
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