Intracervical Vasopressin
Sponsor: Prisma Health-Upstate • ClinicalTrials.gov ID: NCT07102615
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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.
Interventions
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Intracervical injection of Vasopressin
(Drug)
Intracervical injection of Vasopressin
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Intracervical Injection of saline
(Drug)
Intracervical Injection of saline
Eligibility criteria
Conditions
Locations
- The OB/GYN Center — Greenville, South Carolina, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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