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RECRUITING
NCT06998641
NA

EFFECTİVİTY OF CHITOSAN COVERED GAUZE IN POSTPARTUM HEMORRHAGIC OBSTETRIC LACERATIONS

Sponsor: Istanbul Training and Research Hospital

View on ClinicalTrials.gov

Summary

This study was planned to investigate the efficacy of different treatment methods that can be used in the treatment of hemorrhagic tears that may occur in the postpartum period. The volunteers who will participate in the study will be evaluated during the hospitalization period after delivery and at the end of the puerperium 6 weeks after delivery, in accordance with routine postpartum control examinations. In the treatment of postpartum hemorrhagic tears, the treatment options such as suturing the tears to stop bleeding or applying tampons with bleeding stopping agent (chitosan) and compression effect to the torn area will be determined completely randomly.

Key Details

Gender

FEMALE

Age Range

18 Years - 48 Years

Study Type

INTERVENTIONAL

Enrollment

62

Start Date

2025-03-01

Completion Date

2028-12

Last Updated

2025-05-31

Healthy Volunteers

No

Interventions

PROCEDURE

Chitosan-covered-gauze application

Effectiveness of chitosan-covered-gauze in terms of patients' comfort and satisfaction, hospital stay, total amount of bleeding, hemoglobin decline and other complications (infections, need for transfusion etc.) for the treatment of hemorrhagic obstetrical tears

PROCEDURE

Suturation

Effectiveness of suturation in terms of patients' comfort and satisfaction, hospital stay, total amount of bleeding, hemoglobin decline and other complications (infections, need for transfusion etc.) for the treatment of hemorrhagic obstetrical tears

Locations (1)

Istanbul Training and Research Hospital Department of Obstetrics and Gynecology

Istanbul, Turkey (Türkiye)