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临床试验/CTRI/2026/01/102488
CTRI/2026/01/102488尚未招募4 期

A Randomized Controlled Trial Comparing the Efficacy of Five Percent Dextrose and Triamcinolone Hydrodissection for Carpal Tunnel Syndrome

AIIMS Jodhpur1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2026年1月30日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
AIIMS Jodhpur
入组人数
110
试验地点
1

研究概览

简要总结

Carpal Tunnel Syndrome is the most common entrapment neuropathy resulting from compression of the median nerve within the carpal tunnel, leading to pain, numbness, and weakness in the hand. Hydrodissection, an ultrasound guided technique, separates the median nerve from surrounding tissues to relieve compression and improve nerve mobility. This double blind randomized controlled trial aims to compare the efficacy of five percent dextrose in water and triamcinolone forty milligrams per milliliter hydrodissection in patients with mild to moderate Carpal Tunnel Syndrome. A total of 110 participants, 55 in each group, will be recruited from the Department of Physical Medicine and Rehabilitation at the All India Institute of Medical Sciences, Jodhpur. Group A will receive a 10 milliliter injectate of five percent dextrose in water, consisting of 2 milliliters of 25 percent dextrose, 3 milliliters of two percent lidocaine, and 5 milliliters of normal saline. Group B will receive 10 milliliters of triamcinolone preparation, consisting of 1 milliliter triamcinolone, 3 milliliters of two percent lidocaine, and 6 milliliters of normal saline. Injections will be performed under ultrasound guidance using an in plane ulnar approach. Outcomes including pain score using visual analog scale, Boston Carpal Tunnel Syndrome Questionnaire, ultrasound measured cross sectional area, nerve conduction studies, and grip strength will be assessed at baseline, 1 month, and 3 months. Five percent dextrose in water hydrodissection is hypothesized to provide longer lasting pain relief and functional improvement compared to triamcinolone.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
20.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Patients diagnosed with mild to moderate carpal tunnel syndrome based on electrophysiological studies and meeting the following criteria.
  • Primary symptom includes nocturnal paresthesia or dysesthesia in the affected hand, possibly associated with hand posture, overuse, or relief by shaking the hand, also known as the flick sign.
  • At least one of the following features must be present.
  • Numbness in the median nerve sensory distribution of the hand.
  • Weakness with atrophy of the thenar muscles.
  • Positive Phalen’s sign or Tinel’s sign.

排除标准

  • Pre existing neurological conditions such as polyneuropathy, brachial plexopathy, or thoracic outlet syndrome.
  • Recent wrist surgery.
  • Inflammatory conditions such as rheumatoid arthritis, hypothyroidism, or other rheumatological disorders.
  • Uncontrolled diabetes mellitus.
  • Current warfarin use or previous steroid injections at the wrist.
  • Any trauma, tumor, or infection at the injection site.
  • Allergy to corticosteroids or lidocaine.

研究者

发起方
AIIMS Jodhpur
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Ravi Gaur

All India Institute Of Medical Sciences Jodhpur

研究点 (1)

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