Pregnancy in Diabetic Clinical Trials
2 recruiting trials for Pregnancy in Diabetic. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Pregnancy in Diabetic clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Turku University Hospital (1), Ohio State University (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Immediate inpatient postpartum OGTT (diagnostic_test, 1 trial), followed by Standard of care 4-12 week postpartum OGTT.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
Noninvasive Evaluation of Fetal Hyperinsulinemia With Ultrasound Radiomics
The goal of this observational study is to compare fetal liver ultrasound radiomics between pregnancies complicated by type 1 diabetes and healthy controls. The main questions it...
A Randomized Controlled Trial of Diabetes Screening Immediately Postpartum (DIP) and Follow Up PP CARE
DIP : To conduct a pragmatic, non-blinded randomized controlled trial (pRCT) of immediate in-patient postpartum OGTT prior to delivery discharge (intervention) versus 4-12 week...
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Frequently Asked Questions
There are currently 2 clinical trials for Pregnancy in Diabetic, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Pregnancy in Diabetic, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Pregnancy in Diabetic, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.