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A randomized controlled trial was done on 127 women planned for TLH, and divided into two groups; group A includes women that underwent conventional TLH, and group B includes women that underwent TLH with prior uterine artery ligation at its origin. Both grouped were compared regarding the blood loss, operation time, intraoperative complications and post-operative follow-up.
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Inclusion Criteria: any benign uterine pathology such as:
Exclusion Criteria:
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127 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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