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临床试验/NCT07525687
NCT07525687招募中不适用

Temporary Uterine Tourniquet Application Versus Local Myometrial Epinephrine Injection During Laparoscopic Myomectomy

Minia University1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2026年4月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
74
试验地点
1
主要终点
Intraoperative Blood Loss

研究概览

简要总结

While both local vasoconstrictors and tourniquet application are recognized methods for blood loss control, there is a paucity of head-to-head randomized controlled trials directly comparing these two distinct approaches in laparoscopic myomectomy. Existing data often compare these methods to no intervention or to other less common techniques. A direct comparison is essential to determine which method offers superior hemostasis with an acceptable safety profile in the laparoscopic setting. This study aims to address this gap in the literature.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients aged 18-45 years.
  • Diagnosed with symptomatic uterine leiomyomas requiring laparoscopic myomectomy.
  • Presence of at least one myoma with a diameter ≥3 cm and ≤10 cm.
  • Patients with up to 3 myomas (to standardize surgical complexity).
  • Preoperative hemoglobin level ≥10 g/dL.
  • Ability to provide informed consent.

排除标准

  • Patients with more than 3 myomas or any myoma larger than 10 cm.
  • Patients with suspected uterine malignancy (e.g., leiomyosarcoma).
  • Patients with known bleeding disorders or on anticoagulant therapy that cannot be safely discontinued.
  • Patients with significant cardiovascular disease, uncontrolled hypertension, or arrhythmias (relative contraindications for epinephrine).
  • Patients with active pelvic infection.
  • Patients with previous extensive uterine surgery (e.g., multiple prior myomectomies or extensive uterine reconstruction) that may compromise uterine integrity.
  • Patients undergoing concurrent major gynecological procedures that might significantly affect blood loss (e.g., hysterectomy, extensive adhesiolysis).
  • Patients with known allergy to epinephrine.
  • Patients unwilling or unable to comply with follow-up protocols.

研究组 & 干预措施

Local Myometrial Epinephrine Injection

Active Comparator

干预措施: Local Myometrial Epinephrine Injection (Procedure)

Temporary Uterine Tourniquet Application

Active Comparator

干预措施: Temporary Uterine Tourniquet Application (Procedure)

结局指标

主要结局

Intraoperative Blood Loss

时间窗: During operation

次要结局

未报告次要终点

研究者

发起方
Minia University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohamed Hassan Mohamed Abdel Ghfar

Lecturer of Obstetrics and Gynecology

Minia University

研究点 (1)

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