CTRI/2024/04/065917尚未招募2 期
The efficacy of perioperative para-cervical block with 0.25% bupivicaine as an adjuvant with intravenous paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy - nil
Sri Manakula Vinayagar Medical College and Hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
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.Age between 18 and 65 years
- •2.American Society of Anesthesiologists physical status (ASAPS) classification I-II
- •3.Planned for laparoscopic hysterectomy (includes total laparoscopic hysterectomy, laparoscopic supracervical hysterectomy, laparoscopically assisted vaginal hysterectomy, with or without salpingo-oophorectomy)
排除标准
- •1.History of cervical surgery such as conization or cerclage.
- •2.Inability to perform the para-cervical block due to anatomical abnormalities (i.e., very atrophicor small cervix).
- •3.Allergy to bupivacaine, planned concomitant surgical procedures involving extensive
- •additional tissue manipulation such as pelvic lymph node dissection.
- •4.Previously taking opioids for chronic pain.
- •5.Chronic PID, endometriosis
研究者
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