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临床试验/NCT03587025
NCT03587025已完成3 期

Preemptive Analgesia With Amitryptyline for Prevention of Post-operative Pain in Women After Total Abdominal Hysterectomy: a Randomized Clinical Trial

University of Campinas, Brazil1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2015年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
150
试验地点
1
主要终点
Effectiveness of amitryptyline in the prevention of post-operative pain in women undergoing total abdominal hysterectomy, twenty-four hours after surgery

研究概览

简要总结

The purpose of this study is to determine whether amitryptyline is effective in the prevention of pain in women after a total abdominal hysterectomy.

详细描述

It will be performed a randomized clinical trial, double-blind, placebo-controlled, with two branches: one group receiving preemptive analgesia with amitryptyline and one receiving placebo. Blind procedures (blinding):

  1. The participant does not know which group participates;
  2. The evaluator does not know to which group it belongs to every individual;
  3. The tablets provided to patients will be identical.

Study population All patients with total abdominal hysterectomy indication attended in Gynecological Surgery clinic of the Hospital Pedro I.

Sample

It will be obtained a non-consecutive probability sample offering to participate in the study to all women that is going to be submitted to total abdominal hysterectomy indication in the referral hospital from june 2015 to june 2016. Then these will be submitted to randomization process as explained later.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women scheduled for total abdominal hysterectomy for benign conditions (e.g. hemorrhagic and / or uterine fibroid disorder);
  • Age between 18 and 60;

排除标准

  • Endometriosis;
  • Abnormal cervicovaginal smears;
  • Uterine prolapse;
  • Patients with a history of intolerance to opioids or narcotics;
  • Patients with contraindications to the use of amitriptyline (e.g., ischemic heart disease, glaucoma)
  • addicted to alcohol or drugs;
  • Use of analgesics in the 24 hours prior to the possible administration of amitriptyline;
  • Failure to provide informed consent;
  • Different anesthesia from spinal anesthesia

研究组 & 干预措施

Amitryptyline

Active Comparator

Patients who will be take amitryptyline, 75mg, only use, 30min before surgery.

干预措施: Amitriptyline (Drug)

Placebo

Placebo Comparator

Patients who will be take placebo 30min before surgery.

干预措施: Placebo (Drug)

结局指标

主要结局

Effectiveness of amitryptyline in the prevention of post-operative pain in women undergoing total abdominal hysterectomy, twenty-four hours after surgery

时间窗: Twenty-four hours after surgery

The postoperative pain will be measured twenty-four hours after surgery, using the visual pain scale (0 - no pain to 10 - very hard pain)

次要结局

  • Intensity of acute postoperative pain twelve hours after the procedure(Twelve hours after the procedure)
  • Intensity of acute postoperative pain twenty-four hours after the procedure(Twenty-four hours after the procedure)
  • Records of rescue analgesia(From the end of the procedure until 48 hours after that)
  • Frequency of adverse effects(From the end of the procedure until 48 hours after that)
  • Effectiveness of amitryptyline in the prevention of post-operative pain in women undergoing total abdominal hysterectomy, forty-eight hours after surgery(Forty-eight hours after surgery)
  • Intensity of acute postoperative pain forty-eight hours after the procedure(forty-eight hours after the procedure)
  • Length of hospitalization(participants will be followed for the duration of hospital saty, an expected average of 48 hours.)
  • Intensity of acute postoperative pain six hours after the procedure(Six hours after the procedure)
  • Compare surgical time (duration, in minutes) and frequency of intraoperative and postoperative complications(From the end of the procedure until sixty days after that.)
  • Effectiveness of amitryptyline in the prevention of post-operative pain in women undergoing total abdominal hysterectomy, six hours after surgery(Six hours after surgery.)
  • Effectiveness of amitryptyline in the prevention of post-operative pain in women undergoing total abdominal hysterectomy, twelve hours after surgery(Twelve hours after surgery)

研究者

发起方
University of Campinas, Brazil
申办方类型
Other
责任方
Principal Investigator
主要研究者

Antonio Henriques de França Neto

Principal Investigator

University of Campinas, Brazil

研究点 (1)

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