Belfort Dildy- Obstetrical Tamponade System Post-Marketing Surveillance Program

Stopped early

Conditions studied: Postpartum Uterine Bleeding

In brief

This is an open, post-marketing surveillance study obtaining data retrospectively on 300 women, of any age, treated with the BD-OTS for postpartum uterine bleeding.

Key facts

Study ID

NCT01198652

Run by

Glenveigh Medical

People needed

300

Starts

2010-09-01

Expected to finish

2012-10-01

Last updated by the study team

2013-03-05

Who can join

Age: any. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Treatment with the BD-OTS device

You may not qualify if…

• None

Where it is running

• Banner Good Samaritan Medical Center — Phoenix, Arizona, United States
• Presbyterian/St. Luke's Medical Center — Denver, Colorado, United States
• Orlando Health — Orlando, Florida, United States
• Monmouth Medical Center — Long Branch, New Jersey, United States
• UHS - Wilson Medical Center — Johnson City, New York, United States
• University of Cincinnati — Cincinnati, Ohio, United States
• Toledo Hospital — Toledo, Ohio, United States
• Medical University of South Carolina — Charleston, South Carolina, United States
• Erlanger — Chattanooga, Tennessee, United States
• St. David's Medical Center — Austin, Texas, United States
• North Austin Medical Center - St. David's Women's Center of Texas — Austin, Texas, United States

Full record on ClinicalTrials.gov

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