RecruitingNot ApplicableNCT06359886
B-lynch Transverse Compression Suture
B-lynch Transverse Compression Suture in the Prophylaxis and Control of Postpartum Heamorrhage in Patients With Placenta Previa: A Pilot Study
Sponsor
Alexandria University
Enrollment
25 participants
Start Date
Mar 20, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
Is B-Lynch transverse compression suture safe and effective in controlling excessive blood loss during conservative management of women with placenta previa?
Eligibility
Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years
Inclusion Criteria3
- Single gestation
- Elective CS for placenta preiva (diagnosed by transvaginal ultrasound).
- Muliparity (para 2 or more).
Exclusion Criteria14
- Morbidly adherent placenta: accrete, increta or percreta, diagnosed by abdominal and/or transvaginal ultrasound.
- Ultrasonographic features of morbidly adherent placentas:
- Loss of Retro-placental sonolucent zone.
- Vascular lacunae.
- Myometrial thinning.
- Interruption of the bladder border.
- More than 3 previous C.S.
- Severely haemodynamic instablility needing immediate hysterectomy.
- Patients with the cardiac, hepatic, renal or thromboembolic disease
- Patients with coagulopathy:
- Receiving anticoagulant therapy.
- With thrombocytopenia or thrombasthenia.
- Known coagulation factor defect.
- Distorted uterus as unicornuate, bicornuate, fibroid uterus and adenomyosis uteri.
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Interventions
PROCEDUREB-Lynch Transverse Compression Suture
closure of uterine and utero ovarian arteries bilaterally with one suture
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06359886
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