Cohort Study of Risk Reducing Salpingectomy

Completed · Not applicable

Conditions studied: Sterilization, Tubal, Salpingectomy, Ovary, Prevention & Control

In brief

Women undergoing surgical sterilization will be interested in risk reducing salpingectomy, and surgeons performing the procedure will be able to successfully complete the salpingectomy.

Key facts

Study ID

NCT02165709

Run by

University of North Carolina, Chapel Hill

People needed

18

Starts

2014-06-01

Expected to finish

2015-09-01

Last updated by the study team

2017-04-25

Who can join

Age: 35 and older, up to 60. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women > 35 years requesting sterilization as interval procedure OR at time of cesarean delivery
• At least one living child
• English or Spanish speaking
• Sterilization planned as interval (laparoscopic) procedure via Family Planning Clinic services or at time of delivery
• Delivery by cesarean section (planned or following labor)

You may not qualify if…

• Age < 30
• Medical complications that increase risk for surgical bleeding (e.g. Idiopathic thrombocytopenic purpura (ITP); von Willebrand disease (vWD); need for prophylactic or therapeutic anticoagulation)

Where it is running

• University of North Carolina Hosptials — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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