Menstruation Clinical 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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Found 86 clinical trials
A Prospective Observational Study of Outcomes from Proximal Thoracic Aortic Disease

Both repairs are high risk since blood flow to your brain and the rest of your body may be damaged or blocked for a period of time. Data collected over a one year period may give the surgeon more information about risks procedure in this patient population.

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  • 19 Feb, 2024
  • 1 location
Study Evaluating the Efficacy of Synergo Radiofrequency-Induced Thermochemotherapy Effect (RITE) with Mitomycin C (Synergo RITE + MMC) in CIS Non-Muscle Invasive Bladder Cancer (NMIBC)

., MMC) is continuously circulated between the bladder and the computer-embedded Synergo® radiofrequency hyperthermia device. The study will consist of three periods: 1) Screening; 2) Induction treatment (8 weekly treatments of Synergo® RITE + MMC), and 3) Maintenance treatment and follow-up (one Synergo® RITE + MMC treatment every 6 weeks).

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  • 19 Feb, 2024
  • 1 location
A Phase 3 Randomized Double-blind Placebo-controlled Study to Assess the Efficacy and Safety of BIVV009 in Patients with Primary Cold Agglutinin Disease Without a Recent History of Blood Transfusion (Cadenza)

For the purpose of marketing authorization application, an interim analysis of safety and efficacy data will be performed after all patients have completed the double-blind treatment period (Part A). The Part B open-label extension study will run for 1 year following last patient out (LPO) under Part A.

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  • 19 Feb, 2024
  • 1 location
Randomized Study of Cranial Blocks for Postoperative Anesthesia to Reduce Pain and Postoperative Opioid Usage

The research study is being conducted to look at the effectiveness of analgesia (pain medication) by scalp nerve block with various medications that will help doctors to more effectively control pain after surgery and for a longer period of time. 

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  • 19 Feb, 2024
  • 1 location
Skeletal Muscle Perfusion and Mitochondrial Function in Heart Failure with Preserved Ejection Fraction

The most common risks of participation are feeling uncomfortable in the MRI scanner due to lying still on the MRI table for prolonged periods of time, feeling claustrophobic in the MRI scanner (although your head will not be in the scanner), and minor leg discomfort from being asked to exercise …

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  • 19 Feb, 2024
  • 1 location
[18F]FLUOROPROPYL-TRIMETHOPRIM (F-TMP) PET/CT IMAGING TO EVALUATE BIODISTRIBUTION AND KINETICS IN HUMAN SUBJECTS

The Biodistribution cohort will include up to 5 patients who will undergo a series of vertex to mid-thigh biodistribution [18F]F-TMP PET/CT scans over a period of approximately 3 ½ hours. The Dynamic cohort will include up to 15 patients who will undergo approximately 60 minutes of dynamic scanning followed by …

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  • 19 Feb, 2024
  • 1 location
An Open-Label Study to Evaluate the Safety and Tolerability of PCS499 for the treatment of Necrobiosis Lipoidica

The main purpose of this research study is to test the safety and tolerability of PCS499 when given to individuals at a dose of 300 mg, twice a day for 1 week followed by giving PCS499 to individuals at a dose of 900 mg, twice a day, for remaining treatment …

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  • 19 Feb, 2024
  • 1 location
A Phase 2 Dose Ranging Study to Evaluate the Efficacy and Safety of AMG 570 in Subjects with Active Systemic Lupus Erythematosus (SLE) with Inadequate Response to Standard of Care (SOC) Therapy

Study duration for a single subject will be 52 weeks plus the screening period and required 16 weeks safety follow-up period consisting of 4 visits. There are 33 total visits. Target enrollment: 300 people, about 80 sites.

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  • 19 Feb, 2024
  • 1 location
An Open Label Study to Assess the Safety and Efficacy of COR-003(2S 4R-Ketoconazole) in the Treatment of Endogenous Cushing's Syndrome

The study will involve 90 people with Cushings disease in North America and in certain European countries. The study will begin with a screening period followed by a dose finding phase, lasting 2-16 weeks, to determine the most effective and tolerable maximum dose for an individual subject.

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  • 19 Feb, 2024
  • 1 location
The 1289-0032 Research Study for people at risk of psychosis

The early symptoms may include: -trouble thinking clearly or concentrating -believing or hearing things that others do not -losing control of your thoughts -feeling nervous or anxious -feeling that others are "out to get" you -having trouble with family and friends -having thoughts that scare you or the people are …

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  • 19 Feb, 2024
  • 1 location