评估米索前列醇两种方案在中期妊娠终止中的疗效——一项随机比较

Rabia Kurshid, Abida Ahmed, S. Mir, I. Shamas
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引用次数: 4

摘要

我们对妊娠19-23周接受医学终止妊娠的患者进行了一项随机临床试验。所有患者均接受800 m gm阴道米索前列醇治疗,并随机分配至400 m gm口服米索前列醇或400 m gm阴道米索前列醇每8小时一次,最多4次剂量。比较两组的疗效和不良反应。比较两组平均引产时间。
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To Assess The Efficacy Of Two Regimens Of Misoprostol For Second Trimester Pregnancy Termination-A Randomized Comparison
:We performed a randomized clinical trial in patients who were at 19-23 weeks gestation who were admitted for medical termination of pregnancy. All patients received 800 m gm of vaginal misoprostol and were assigned randomly to 400 m gm of oral misoprostol or 400 m gm of vaginal misoprostol every 8 hourly up to a maximum of 4 doses. Efficacy and side effects were compared. The mean induction abortion interval was compared in both groups.
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