PACTR202103517062817已完成未知
REDUCING BLOOD LOSS DURING ABDOMINAL MYOMECTOMY: SUBLINGUAL MISOPROSTOL WITH PERICERVICAL TOURNIQUET VERSUS PERICERVICAL TOURNIQUET ALONE; A RANDOMIZED CONTROL TRIA
Adebayo M.D. Agboola0 个研究点目标入组 68 人开始时间: 2021年3月12日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 68
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •1.Patients presenting for abdominal myomectomy with documented uterine fibroids on pelvic imaging.
- •2.Age > 18years.
- •3.Pre-menopausal women
- •4.Pre-operative hematocrit >30%
- •5.Women willing to have sublingual administration of misoprostol or a placebo pre-procedure.
- •6.No other pre-operative medical intervention to reduce blood loss during abdominal myomectomy.
- •7.Consultant-led Abdominal myomectomy.
- •8.Regional anaesthesia for Abdominal myomectomy
- •9.Ability to understand and the willingness to sign a written informed consent.
排除标准
- •1.Patients who have had a prior abdominal myomectomy
- •2.Post-menopausal women
- •3.Patients with a history of gynecologic malignancy
- •4.Patients with known bleeding/clotting disorders
- •5.Patients on anticoagulant therapy.
- •6.History of allergic reactions attributed to misoprostol or compounds of similar chemical or biologic composition to misoprostol
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