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临床试验/PACTR202106887906354
PACTR202106887906354招募中3 期

Adjunctive Uterine Incision compression versus tourniquet alone for reduction of blood loss during abdominal myomectomy; a randomized controlled trial

Babcock University0 个研究点目标入组 240 人开始时间: 2021年5月29日最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
240

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

  • Patients aged 18-45 years, undergoing abdominal myomectomy.
  • Patients with uterine fibroids without adhesive complcations.
  • Patients fibroid undergoing myomectomy for the first time.

排除标准

  • History of coagulopathy, or heart disease, or myocardial infarction, or hypertension, or diabetes, or sickle cell disease, or kidney disease
  • Pre-operative PCV <30%.
  • Patients with thromboembolic disease, or on anticoagulants'
  • History of allergy to tranexamic acid or vasopressin or ergometrine.
  • History of previous myomectomy or previous extensive pelvic surgery or features suggestive of pelvic adhesions. Patients who would not accept blood transfusion.
  • History or imaging features suspicious of malignancy.
  • Entirely subserosal fibroids or entirely submucous fibroids that do not involve intramural incisions and fibroid enucleation.
  • Laparoscopic, hysteroscopic or combinations of either with abdominal myomectomy.

研究者

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