Clinical Trial

Intracervical Vasopressin

Recruiting Phase 4
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Record status
This record was last updated November 4, 2025 (before its estimated August 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
This randomized study looks at whether using a medicine injected into the cervix of the uterus (intracervical), called vasopressin, helps to achieve better removal of retained products of conception (RPOC). RPOC means that after a pregnancy has ended (through miscarriage, abortion, or delivery), some parts of the pregnancy tissue, usually from the placenta or fetus, have stayed in the uterus. A hysteroscopic removal of RPOC is one type of treatment. This is a surgical procedure where a doctor uses a small camera attached to a thin tube (called a hysteroscope) to look inside the uterus. The main goal of the study is : • To add to the existing research through this study to see if the injection of intracervical vasopressin leads to improved completion rates of hysteroscopic management of RPOC. Participants will: • would be randomized to receive either vasopressin intracervical injection or a placebo injection (non-active saline) during your procedure. Information from the procedure will be collected from the participant's medical record.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-07-31; most recent amendment 2025-10-31.
Status change: Not Yet Recruiting → Recruiting 2025-10-31
Trial Details
NCT Number NCT07102615
Lead Sponsor Prisma Health-Upstate
Conditions Retained Products of Conception
Enrollment 50 participants
Start Date 2025-10-30
Primary Completion 2026-08-01 (estimated)
Study Completion 2026-12-01 (estimated)
Updated on ClinicalTrials.gov 2025-11-04