Intracervical Vasopressin
Recruiting
Phase 4
Interventional Study
Retained Products of Conception
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 – 51
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 50 (estimated)
- Sponsor
- Prisma Health-Upstate · Other
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About This Trial
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 hy…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women
* Aged 18-51
* Undergoing surgical management for retained products of conception, postpartum retained products of conception or 1st trimester missed or incomplete abortion
Exclusion Criteria:
* Hemodynamic instability
* Active hemorrhage- soaking pad/hour
* Allergy to…
Contacts