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临床试验/ACTRN12621000973819
ACTRN12621000973819招募中4 期

Effect of Paracervical Block on Post-operative Pain Following Benign Laparoscopic Hysterectomy: Objective Evaluation Of Parameters By Utilising A Single Centre Double Blind Randomized Controlled Trial

Tarana Lucky0 个研究点目标入组 67 人开始时间: 2021年7月26日最近更新:

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
67

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • 1.Age greater than or equal to 18 years
  • 2.Undergoing a total laparoscopic hysterectomy for benign indications (elective)
  • 3.Indication of prophylactic surgery for at-risk patients can be included
  • 4.With or without the following concurrent procedures:
  • a.Unilateral or bilateral salpingo-oophorectomy
  • b.Excision of endometriosis (below pelvic brim)

排除标准

  • 1.Allergy to either of Bupivacaine, Adrenaline, or any amide anaesthetics or opioids
  • 2.Any other contraindications to Adrenaline or Bupivacaine
  • 3.Weight <50kg or >100kg
  • 4.Emergency hysterectomy
  • 5.For non-English speaking participants: Unable to collect data adequately despite use of language interpreter
  • 6.Excision of endometriosis that is above pelvic brim
  • 7.Concurrent bowel or upper abdominal surgery
  • 8.Chronic pain requiring ongoing opioid analgesia
  • 9.Any indication of malignancy pre-op
  • 10.Any intra-op suspicion/detection of malignancy requiring lymph node dissection
  • 11.Any concomitant vaginal procedures (prolapse repair, mid-urethral slings, etc.)
  • 12.Intraoperative conversion to laparotomy
  • 13.Inability to perform the paracervical block due to anatomic abnormalities
  • 14.Intraoperative injury to gastrointestinal or urologic tract that necessitated repair
  • 15.Patient needing return to OT for complications
  • 16.Procedures requiring extensive additional tissue manipulation such as:
  • a.Pelvic lymph node dissection
  • b.Laparoscopic pelvic floor repair procedures

研究者

发起方
Tarana Lucky

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