Actively Recruiting
EFFECTİVİTY OF CHITOSAN COVERED GAUZE IN POSTPARTUM HEMORRHAGIC OBSTETRIC LACERATIONS
Led by Istanbul Training and Research Hospital · Updated on 2025-05-31
62
Participants Needed
1
Research Sites
195 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
EFFECTİVİTY OF CHITOSAN COVERED GAUZE IN POSTPARTUM HEMORRHAGIC OBSTETRIC LACERATIONS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patients aged 18 to 48 years
- Gave birth at Istanbul TRH between March 2025 and March 2027
- Experienced first or second degree obstetric lacerations with postpartum hemorrhage
- No need for anatomical defect repair
- No additional conditions affecting postpartum bleeding such as uterine atony or placental remnants
You will not qualify if you...
- Outside the age range of 18 to 48 years
- Did not give birth at Istanbul TRH between March 2025 and March 2027
- Obstetric lacerations requiring anatomical defect repair
- Presence of additional conditions affecting postpartum bleeding such as uterine atony or placental remnants
AI-Screening
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Trial Site Locations
Total: 1 location
1
Istanbul Training and Research Hospital Department of Obstetrics and Gynecology
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
D
Doruk C Katlan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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