MedPath

Database of Monochorionic Pregnancies

Recruiting
Conditions
Monochorionic Diamniotic Placenta
Monochorial Monoamniotic Placenta
Twin to Twin Transfusion Syndrome
Twin; Complicating Pregnancy
Twin Reversal Arterial Perfusion Syndrome
Registration Number
NCT05543499
Lead Sponsor
University of Miami
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1200
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Number of participants with Preterm DeliveryUp to 42 weeks gestation

Preterm delivery is defined as birth \<37 weeks gestation

Number of participant with Premature Spontaneous Rupture of the MembranesUp to 42 weeks

As per clinical evaluation

Number of Infant DeathsUp to 12 months post infant delivery

The Number of Infant Deaths

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Miami

🇺🇸

Miami, Florida, United States

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