跳至主要内容
临床试验/TCTR20200530003
TCTR20200530003招募中2 期

Comparison of anterior carpal pain, functional outcome and time to return to work between minimal invasive surgery versus standard open technique in carpal tunnel syndrome in early postoperative period, prospective randomized control trial.

Faculty of Medicine, Chiang Mai University0 个研究点目标入组 12 人开始时间: 2020年5月30日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
15 Years 至 85 Years(—)
性别
All

入选标准

  • Male or female, age between 15-85 years who was diagnosed as carpal tunnel syndrome following the criteria from practice parameter for carpal tunnel syndrome (summary statement). Report of the Quality Standards Subcommittee of the American Academy of Neurology.Neurology 1993;43:2406-9 and decide to treat with operative treatment. All participants will be performed electrodiagnosis.

排除标准

  • Patient who had history of local anesthetic drug, NSAID allergy, previous wrist surgery, previous distal radius fracture, underlying rheumatoid arthritis, gout, hypothyroidism, pregnancy at date of enrollment, active cervical radiculopathy, active elbow or shoulder pain at date of enrollment.
  • After informed and consent, participant was randomized into one of two groups which is standard open technique (S group) or mini-open technique (M group) by minimization randomization method (severity, DM). Concealment was performed by opaque envelope. Blinding was performed for patient (special dressing not allow to see the surgical incision) and assessor until 2 weeks after operation.

研究者

相似试验