CTRI/2017/09/009677已完成3 期
To compare the efficacy of Intramyometrial Vasopressin plus Rectal Misoprostol with Intramyometrial Vasopressin alone to decrease blood loss during Laparoscopic Myomectomy: A Randomised Clinical Trial
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Women between 16-45 years of age
- •2.Myomatous uterus corresponding to 28 weeks size or less
- •3.Largest fibroid less than 15 cm
- •4.Haemoglobin level equal to or greater than 9 g/dL
- •5.No contraindication to use of vasopressin or misoprostol (renal/heart
排除标准
- •1.Previous myomectomy
- •2.Significant medical condition such as heart, renal or pulmonary disease
- •3.Hb < 9 g/dL
- •4.Pregnancy
- •5.History of any bleeding disorder
- •6.Concurrent anticoagulation therapy
- •7.Grade 0 submucosal fibroid
- •8.Patient not fit for laparoscopic surgery
研究者
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