Active — Not RecruitingNot Applicable

Database of Monochorionic Pregnancies

United States1,200 participantsStarted 2022-10-01

Plain-language summary

The purpose of this study is to collect and analyze data regarding natural history, indications for fetal interventions, and maternal and fetal/neonatal outcomes associated with complicated monochorionic twin pregnancy.

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * The study population will consist of MC pregnancies (maternal, fetal, and neonatal data) that have undergone evaluation and/or treatment for complications attributable to monochorionic twin pregnancy at the University of Miami. * Maternal age 18 years and older. Exclusion Criteria: * Participation declined or consent not granted in prospective arm * Loss to follow-up

What they're measuring

Number of participants with Preterm Delivery

Timeframe: Up to 42 weeks gestation

Number of participant with Premature Spontaneous Rupture of the Membranes

Timeframe: Up to 42 weeks

Number of Infant Deaths

Timeframe: Up to 12 months post infant delivery

Trial details

NCT IDNCT05543499

SponsorUniversity of Miami

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-12-01

View on ClinicalTrials.gov More Monochorionic Diamniotic Placenta trials