Found 11 Type 2 Diabetes Mellitus trials
A listing of Type 2 Diabetes Mellitus medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
The purpose of this prospective observational study is to gather practical use data of the Dexcom G7 rtCGM system utilized throughout pregnancy among patients with gestational diabetes (GDM). Primary Study Objective: (1) To generate data on the practical use of rtCGM to manage pregnancy in patients with GDM (2) To …
Are you at risk for type 1 diabetes?Are you willing to receive a phone call every 6 months?For patients treated with TZIELD AND NOT treated with TZIELDYou may qualify to participate in an observational research studyAn observational study (you will not receive any experimental medication)Does not require on-site visitsParticipation will …
Determine whether oral BHB supplementation is safe and tolerable in FAP. Determine whether oral BHB supplementations increases serum BHB levels in FAP. Investigate whether oral BHB supplementation leads to transcription and protein expression changes in the intestinal mucosa and polyps in FAP. Elucidate whether oral BHB supplementation in FAP reduces …
To determine the changes in symptoms and functional limitations in patients with symptomatic hypertrophic cardiomyopathy (HCM) treated with sotagliflozin as compared to placebo.
The objective of this study is to complete a pre-implementation inquiry at RHD to assess barrier and facilitators to implementing a new intervention and assess awareness, acceptability and knowledge of HIV prevention modalities like PrEP among staff and residents. Narrative summaries will be generated for each participant, using transcripts and …
Requesting a reliance agreement with an external IRB. The purpose of this double-blind, placebo-controlled trial is to evaluate the safety and efficacy of treatment with plozasiran on the reduction of fasting serum TG from Baseline in subjects with severe hypertriglyceridemia who have fasting TG levels above 500 mg/dL (5.65 mmol/L).
Requesting a reliance agreement with an external IRB. The purpose of this open label extension trial is to evaluate the safety and tolerability of treatment with olezarsen in subjects with severe hypertriglyceridemia who have completed the ISIS 678354-CS5 or -CS6 study with an acceptable safety profile.
To evaluate if use of the Percepta Nasal Swab test in the diagnostic work up of newly identified pulmonary nodules reduces the number of invasive procedures in the group classified as low-risk by the test and that are benign as compared to a control group managed without a Percepta Nasal …
Reliance Agreement requested with VUMC (IREx). Creation of an observational phenotyping cohort of patients with acute respiratory distress syndrome, pneumonia or sepsis. Clinical risk factors, molecular phenotypes, and illness trajectories during the acute and recovery phases of these critical illness syndromes to be assessed. Alteration protocol describes the minimal risk …
Reliance Agreement requested with VUMC (IREx). Creation of an observational phenotyping cohort of patients with acute respiratory distress syndrome, pneumonia or sepsis. Clinical risk factors, molecular phenotypes, and illness trajectories during the acute and recovery phases of these critical illness syndromes to be assessed. Full study protocol (Protocol A) describes …
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