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临床试验/NCT04145791
NCT04145791已完成不适用

Ice Application for Postoperative Pain: a Randomized Control Trial

University of Texas Southwestern Medical Center4 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2019年2月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
74
试验地点
4
主要终点
Pain score of cryotherapy patients as compared to non-cryotherapy patients

研究概览

简要总结

The purpose of the proposed study is to investigate the effectiveness of cryotherapy as an additional form of pain control in women undergoing laparoscopic hysterectomy for benign gynecologic conditions through a randomized trial.

详细描述

The purpose of the proposed study is to investigate the effectiveness of cryotherapy as an additional form of pain control in women undergoing laparoscopic hysterectomy for benign gynecologic conditions through a randomized trial. The following aims will be pursued:

Primary Aim: To determine if cryotherapy patients will have lower pain scores on VAS compared to standard pain management patients.

Primary Hypothesis: Patients receiving cryotherapy will have lower VAS scores compared to patients receiving pain management.

Secondary Aim 1: To determine if cryotherapy will reduce the number of morphine milligram equivalent (MME) compared to patients with standard pain management.

Secondary Hypothesis 1: Patients receiving cryotherapy will have lower MME values compared to patients with standard pain management.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Women undergoing laparoscopic hysterectomy for benign indications within 8 weeks of enrollment
  • Women >18 years of age
  • Non-emergent surgery
  • Non-pregnant
  • Women undergoing laparoscopic hysterectomy with the minimally invasive surgery team

排除标准

  • Requires surgery for urinary incontinence
  • Has acute angle glaucoma
  • Has severe cardiac/respiratory disease
  • Current chronic pain condition (ie chronic pelvic pain, fibromyalgia, chronic low back pain)
  • Chronic use/abuse of opioid medications for greater than 1 week preceding procedure
  • Chronic NSAID use
  • Current treatment of opioid dependence with methadone or buprenorphine
  • Non-English or Non-Spanish speaking
  • Procedure converted to laparotomy

结局指标

主要结局

Pain score of cryotherapy patients as compared to non-cryotherapy patients

时间窗: pain score collected at two weeks post operative.

To determine if cryotherapy patients will have lower pain scores on a visual analog scale (VAS) compared to standard pain management patients at the time of same day discharge. VAS requires that patients mark their level pain along a straight 100mm line. There are no number markings on the scale. The beginning of the line is labeled on the left as "no pain" and the end of the line on the right is labeled as "worst pain imaginable." Once marked by the patient, the distance from beginning of the line to the patient's hash mark is measured in millimeters and that value is recorded as the pain level. The minimum is 0 (no pain) and the maximum is 100 (worst pain imaginable).

次要结局

  • Narcotic usage(postoperative day one)
  • Time to discharge(day of surgery, up to 1440 minutes)
  • Quality of Recovery (QoR)(through study completion to take place at preoperative visit, and post operative day #14.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kimberly Kho

Associate Professor of Medicine

University of Texas Southwestern Medical Center

研究点 (4)

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