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临床试验/NCT03407612
NCT03407612已完成不适用

The Effect of Continuous Passive Motion on Pain Control Following Hip Arthroscopy

Ohio State University1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2013年2月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
54
试验地点
1
主要终点
Change in Patient Satisfaction and Functional Outcome

研究概览

简要总结

The purpose of this study is to measure whether CPM (continuous passive motion) usage improves outcomes following arthroscopic hip surgery that includes labral repair. Investigators tested the hypothesis that CPM usage reduces pain levels and pain medication use and improves function in individuals who undergo hip arthroscopy.

详细描述

Subjects undergoing primary hip arthroscopy for acetabular labral repair were randomized to determine whether they would receive a CPM. Those subjects receiving a CPM were instructed to use it for 4-6 hours daily throughout the first two postoperative weeks. The total number of pain medications and average pain scores over the two weeks, as well as Hip Outcome Score Activity of Daily Living (HOS ADL) scores at standard time points were compared via a two sample t-test and intention-to-treat analysis.

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
None

入排标准

年龄范围
14 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •undergoing hip arthroscopy to repair a torn labrum

排除标准

  • •pregnancy
  • •revision surgery
  • •bilateral surgery

研究组 & 干预措施

CPM

Active Comparator

These subjects received a continuous passive motion (CPM) device and were instructed to use it for 4-6 hours daily throughout the first two postoperative weeks following their arthroscopic labral repair. They were provided adequate education on how to operate the device. The subjects recorded their average usage of the CPM, as well as their personal perception of the CPM, at the postoperative 2 day, 7 day, and 14 day marks.

干预措施: Continuous Passive Motion (Device)

No CPM

No Intervention

No CPM was administered to these subjects.

结局指标

主要结局

Change in Patient Satisfaction and Functional Outcome

时间窗: Baseline and 6 weeks, 12 weeks, and 6 months postoperatively

Hip Outcome Score Activities of Daily Living (HOS ADL) questionnaire completed at specific time points. Completion of the HOS ADL provides a score from 0 to 100, with a higher score corresponding to greater level of function. The improvement preoperative to 6 month postoperative scores was also computed.

次要结局

  • Analgesic Usage(Initial two postoperative weeks)
  • Pain Level(Initial two postoperative weeks)

研究者

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

John Ryan

Medical Doctor

Ohio State University

研究点 (1)

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