Belfort Dildy- Obstetrical Tamponade System Post-Marketing Surveillance Program

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01198652

Enrollment

300

Registered

2010-09-10

Start date

2010-09-30

Completion date

2012-10-31

Last updated

2013-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Uterine Bleeding

Brief summary

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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Healthy volunteers

Inclusion criteria

* Treatment with the BD-OTS device

Exclusion criteria

* None

Countries

United States

Outcome results