CTRI/2025/03/081587尚未招募2/3 期
Efficacy of intravenous tranexamic acid in reducing perioperative blood loss in abdominal hysterectomy- A double blinded randomized controlled trial
Tezpur medical college and hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年3月13日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- estimated blood loss by weight, estimated blood loss by suction drain
研究概览
简要总结
It is a randomized controlled trial where patients undergoing total abdominal hysterectomy for benign conditions will be taken as study group, one group (test) will be randomly allocated to be given tranexamic acid preoperatively and the other (control) group will be given placebo. perioperative blood loss in both the groups will be compared to establish the efficacy of tranexamic acid in reducing perioperative blood loss
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 30.00 Year(s) 至 80.00 Year(s)（—）
- 性别
- Female
入选标准
- •Women undergoing total abdominasl hysterectomy with or without bilateral salpingo-oophorectomy due to myoma, menorrhagia, abnormal uterine bleeding, fibroid, adenomyosis.
排除标准
- •patients with cardiac, renal, thromboembolic disease, adnexal mass and malignancy, pre existing anemia, allergy to tranexamic acid, anti coagulant therapy.
结局指标
主要结局
estimated blood loss by weight, estimated blood loss by suction drain
时间窗: during ot, just postop, upto 24 hours postop
次要结局
- use of topical hemostatics, blood transfusion, drop in hb level(during ot, post-operative upto 24 hours postop)
研究者
satabdi bhattacharjee
Tezpur medical college and hospital
研究点 (1)
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