CompletedNot Applicable

Evaluating the Safety and Efficacy of RUCS in PPH

Turkey (Türkiye)11 participantsStarted 2020-01-01

Plain-language summary

This retrospective observational study aims to evaluate the efficacy and safety of Removable Uterine Compression Sutures (RUCS) in the surgical management of postpartum hemorrhage (PPH). Eleven patients who developed PPH and underwent RUCS between January 2020 and November 2024 at Gaziosmanpaşa Training and Research Hospital were included. The primary outcomes assessed were hemorrhage control and procedure-related complications. Data were collected from patient records and analyzed descriptively.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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Inclusion Criteria: Female patients aged 18 to 45 years Diagnosed with postpartum hemorrhage (PPH) following delivery Treated with Removable Uterine Compression Suture (RUCS) Delivery and treatment performed at Gaziosmanpaşa Training and Research Hospital RUCS performed between January 2020 and November 2024 Complete and accessible medical records Exclusion Criteria: Incomplete or missing medical records Use of alternative surgical techniques other than RUCS Patients outside the age range of 18-45 Cases not treated at Gaziosmanpaşa Training and Research Hospital Postpartum hemorrhage not managed with RUCS

What they're measuring

Hemostasis success rate following RUCS application

Timeframe: Within the first 24 hours post-procedure

Trial details

NCT IDNCT07115355

SponsorHavva Betül Bacak

Sponsor typeOTHER_GOV

Study typeOBSERVATIONAL

Primary completion2024-11-30

View on ClinicalTrials.gov More Postpartum Hemorrhage trials