Placenta Clinical Trials

1 recruiting

Frequently Asked Questions

Common questions about Placenta clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 18 of 8 trials

Recruiting

Placental Imaging Techniques

PregnancyUltrasoundPregnancy Outcomes+5 more
Carilion Clinic60 enrolled1 locationNCT06861309
Recruiting

Placental Biology in Health and Disease

PregnancyPre-EclampsiaFetal Growth Restriction (FGR)+3 more
University of Oxford360 enrolled1 locationNCT07470320
Recruiting
Phase 2

Statin Intervention for Severe Early-Onset Placental Insufficiency. (STATIN-PRE Trial)

Intrauterine Growth Restriction (IUGR)Preeclampsia (PE)Placental Insufficiency
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau154 enrolled2 locationsNCT07098975
Recruiting

PRIOR Study (Pre-eclampsia Risk In Oocyte Recipients)

Pre-EclampsiaOocyte DonationPre-Eclampsia; Complicating Pregnancy+12 more
Copenhagen University Hospital, Hvidovre462 enrolled6 locationsNCT07263490
Recruiting
Phase 3

Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy

Pre-EclampsiaIntrauterine Growth RestrictionAspirin+3 more
Centre Hospitalier Intercommunal Creteil500 enrolled20 locationsNCT04356326
Recruiting

Association of Assisted Reproductive Technologies Parameters With the Perinatal Outcome

PreeclampsiaVasa PreviaFetal Growth Restriction (FGR)+3 more
Aristotle University Of Thessaloniki12,084 enrolled6 locationsNCT06918236
Recruiting
Not Applicable

A Prospective Study on the Role of Karl Storz Curved and Straight Fetoscopes (11508AAK and 11506AAK) for Fetoscopic Intrauterine Procedures

Pregnancy RelatedFetal ConditionsMaternal; Procedure+7 more
Boston Children's Hospital50 enrolled1 locationNCT06056635
Recruiting

Multicenter Prospective Cohort Study of Twin Maternal-Child Dyads in China

Pre-EclampsiaHigh Risk PregnancyTwin Pregnancy, Antepartum Condition or Complication+5 more
Peking University Third Hospital2,000 enrolled11 locationsNCT06414655