UnknownNot Applicable

B-lynch Transverse Compression Suture

Egypt25 participantsStarted 2024-03-20

Plain-language summary

Is B-Lynch transverse compression suture safe and effective in controlling excessive blood loss during conservative management of women with placenta previa?

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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Inclusion criteria

✓. Single gestation
✓. Elective CS for placenta preiva (diagnosed by transvaginal ultrasound).
✓. Muliparity (para 2 or more).

Exclusion criteria

✕. Morbidly adherent placenta: accrete, increta or percreta, diagnosed by abdominal and/or transvaginal ultrasound.
✕. More than 3 previous C.S.
✕. Severely haemodynamic instablility needing immediate hysterectomy.
✕. Patients with the cardiac, hepatic, renal or thromboembolic disease
✕. Patients with coagulopathy:
✕. Distorted uterus as unicornuate, bicornuate, fibroid uterus and adenomyosis uteri.

What they're measuring

Intraoperative blood loss

Timeframe: 2 days following the procedure

Postoperative blood loss

Timeframe: 2 days following the procedure

Number of received blood components

Timeframe: 2 days following the procedure

Peripartum haemoglobin level drop

Timeframe: 2 days following the procedure

Trial details

NCT IDNCT06359886

SponsorAlexandria University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04

Contact for this trial

Ahmed S Zeerban, Msc

+201003119968 Ahmedzeerban@gmail.com

View on ClinicalTrials.gov More Blood Loss, Surgical trials