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临床试验/NCT06785935
NCT06785935进行中(未招募)不适用

Ultrasound-guided Percutaneous Release of A1 Pulley by a Needle Knife Versus Ultrasound-guided Corticosteroid Injection in the Treatment of Trigger Finger: a Randomized Clinical Trial

Mansoura University Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年11月11日最近更新:
干预措施
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
40
试验地点
1
主要终点
Pain intensity using the visual analog scale (VAS) scoring system

研究概览

简要总结

Trigger finger is a common cause of hand disability and pain in the general population. It is a pathologic condition of the digital pulleys and flexor tendons. Although the pathogenesis is incompletely clear and multifactorial, the most common cause of the trigger finger is the thickened flexor tendon and/or thickened first annular (A1) pulley located at the metacarpophalangeal joint. Currently, ultrasound is considered an effective and valuable tool for assessing the trigger finger, providing static and dynamic evaluations of this condition and a comparison with the adjacent normal digits. Recently, it has been reported that ultrasound-guided percutaneous A1 pulley precise release using a needle knife has received increasing attention in the clinical treatment of trigger fingers and achieved good results. To our knowledge, this is the first clinical study comparing the efficacy and safety of ultrasonic-guided percutaneous A1 pulley release with a needle knife and the ultrasonic-guided steroid injection in treating trigger fingers.

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

性别
All
接受健康志愿者

入选标准

  • Idiopathic trigger finger
  • Trigger finger at the level of A1 pulley
  • Trigger finger of Green's grades II or III

排除标准

  • Patients with secondary causes of trigger fingers like diabetes mellitus, rheumatoid arthritis, gout, hypothyroidism, amyloidosis, and sarcoidosis.
  • Patients with a previous history of first annular pulley release or injection.
  • Patients with trigger fingers of Green's grade I and IV.
  • Patients with trigger fingers at any level other than the A1 pulley.

研究组 & 干预措施

Patients undergoing ultrasonography-guided percutaneous A1 pulley release using a needle knife

Active Comparator

干预措施: Needle knife (Device)

结局指标

主要结局

Pain intensity using the visual analog scale (VAS) scoring system

时间窗: Before the procedure as well as after one week, one month, and three months

Functional ability according to the standard quick disabilities of the arm, shoulder, and hand score (Q DASH) questionnaire

时间窗: Before the procedure as well as after one week, one month, and three months

Recurrence: The grade of trigger finger according to Green's classification

时间窗: Before the procedure as well as after one week, one month, and three months

Complications such as inflammation, infection, scarring, wound healing problems, and sensory changes

时间窗: After one week of the procedure

次要结局

未报告次要终点

研究者

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

Nouran Khalid Ibrahim Sallam

Resident of Rheumatology, rehabilitation, and physical medicine department at Mansoura University Hospitals

Mansoura University Hospital

研究点 (1)

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