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Study identifier: NCT07534982 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Success Rates of Expectant vs. Medical Management for Retained Products After First-Trimester Abortion: Randomized Controlled Trial

Condition: Retained Product of Conception After First Trimester Medical Abortion  ·  Sponsor: Yael Yagur

PhaseNA
Planned participants150
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersNo

About this study

This prospective randomized controlled trial evaluates the success of medical versus expectant management for retained products of conception (RPOC) following medical abortion with mifepristone and misoprostol for delayed miscarriage in the first trimester. Women aged 18-45 with sonographic evidence of RPOC (endometrial thickness \>10 mm with Doppler flow) will be randomized into two groups: medical management with misoprostol or expectant management (observation only). Follow-up will include ultrasound evaluations over six weeks to monitor uterine clearance and determine further interventions. Population: 150 participants, with 75 in each group. Inclusion Criteria: Stable women with RPOC after medical abortion, bleeding comparable to menstrual flow, and no fever. Exclusion Criteria: Hemodynamic instability, excessive bleeding, fever, or specific endometrial thickness criteria. Outcome Measures: RPOC resolution, need for surgical intervention, complications, and sonographic changes. Study Duration: Five years. Data on demographics, medical history, and ultrasound findings will be analyzed using SPSS, with results informing optimal management strategies for RPOC after first-trimester medical abortion.

This description comes directly from the study's public registry record.

Talk to the study team

Chen Manor Bar, MD  ·  +972544414211  ·  Manor.chen@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Meir Medical CenterKfar Saba, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT07534982