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临床试验/NCT02885701
NCT02885701已完成不适用

A Prospective, Randomized Controlled Study of Splinting After Mini-Open Carpal Tunnel Release

Anthony L. Logli0 个研究点目标入组 249 人开始时间: 2010年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
249
主要终点
Levine-Katz Symptom Severity Scale (SSS)

研究概览

简要总结

The purpose of this study is to determine if any difference exists among 3 different postoperative splinting regimens- no splint, removable splint, and plaster non-removable splint- following mini-open carpal tunnel release (CTR) surgery.

详细描述

We sought to determine if any significant difference in patient-reported or clinical outcomes existed among 3 different postoperative splinting regimens- no splint, removable splint, and plaster non-removable splint- following mini-open carpal tunnel release (CTR) surgery for symptomatic, isolated, nerve conduction study positive carpal tunnel syndrome (CTS).

A total of 249 patients received a mini-open CTR and were subsequently randomized into 1 of the 3 splinting regimens to be removed at the first postoperative visit 10-14 days later. Patient-reported outcomes included QuickDASH surveys, Levine-Katz Symptom Severity Scale (SSS) and Functional Status Scale (FSS) and Pain at Rest and in Action using a Numerical Pain Rating Scale (NPRS). Clinical outcomes included wrist range of motion (ROM), grip and lateral pinch strengths. All outcomes were evaluated bilaterally at 10-14 days, 6 weeks, 3 months, 6 months and 12 months after surgery. Demographic information was obtained preoperatively and complications were observed for and recorded throughout the study

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
Single (Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients were required to have failed conservative treatment for symptomatic, isolated, nerve conduction study positive CTS.

排除标准

  • Exclusion criteria omitted patients who presented with acute onset CTS, concomitant peripheral neuropathy, metabolic disease, postoperative recurring CTS, or who required another operative procedure during carpal tunnel release.

结局指标

主要结局

Levine-Katz Symptom Severity Scale (SSS)

时间窗: 10-14 days postoperatively

The Levine-Katz Symptom Severity Scale (SSS) assesses pain, weakness, and sensation with 11 questions the patient rates on a 5-point scale with 5 indicating the most difficult; the average score is reported.

QuickDASH

时间窗: 10-14 days postoperatively

The Quick Disabilities of the Arm, Shoulder and Hand (DASH) Outcome Measure was designed in 1998 with the goal of providing a more accurate depiction of the everyday symptoms and handicaps exclusively experienced by a patient with an upper extremity musculoskeletal condition. Designed as a patient-completed questionnaire, the DASH Outcome Measure can be administered multiple times throughout patient care to measure changes in function and symptoms over time

Lateral Pinch Strength

时间窗: 10-14 days postoperatively

Lateral pinch strength was taken with a Preston Pinch Gauge.

Grip Strength

时间窗: 10-14 days postoperatively

Grip strength was taken with a Jamar Dynamometer in the 2nd hand position.

Numerical Pain Rating Scale

时间窗: 10-14 days postoperatively

Patients are asked to describe their level of pain intensity over the last 24 hours. The pain scale anchor points 0 and 10 correspond to no pain and worst imaginable pain, respectively. The NPRS can be used multiple times throughout patient care, but has the greatest value in describing post-operative pain-related morbidity.

Wrist Flexion

时间窗: 10-14 days postoperatively

次要结局

  • Complications(10-14 days postoperatively)
  • Demographic Information(Preoperatively)

研究者

发起方
Anthony L. Logli
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Anthony L. Logli

Student Doctor

OrthoIllinois

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