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.
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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

Patti Parker, BSN

864-455-1510

patti.parker@prismahealth.org

CONTACT

Paul Miller, MD

894-455-1600

paul.miller@prismahealth.org

CONTACT