Actively Recruiting

Phase 4
Age: 18Years - 51Years
FEMALE
NCT07102615

Intracervical Vasopressin

Led by Prisma Health-Upstate · Updated on 2025-11-04

50

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Intracervical Vasopressin

Who Can Participate

Age: 18Years - 51Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women
  • Aged 18-51 years
  • Undergoing surgical management for retained products of conception, postpartum retained products of conception or 1st trimester missed or incomplete abortion
Not Eligible

You will not qualify if you...

  • Hemodynamic instability
  • Active hemorrhage, such as soaking a pad every hour
  • Allergy to vasopressin
  • Concern for intrauterine arteriovenous malformation
  • Inability to consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The OB/GYN Center

Greenville, South Carolina, United States, 29605

Actively Recruiting

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Research Team

P

Patti Parker, BSN

CONTACT

P

Paul Miller, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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