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临床试验/NCT04568993
NCT04568993进行中(未招募)不适用

Patient-reported Outcome After Corticoid Injection for Triggerfinger- a Randomized Controlled Study Between Two Injection Procedures and Between Corticoid Injection and Percutaneous Release

Sahlgrenska University Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年10月1日最近更新:
适应症
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)
发起方
入组人数
100
试验地点
1
主要终点
Impairment of finger motion

研究概览

简要总结

This is a prospective randomized multicenterstudy focusing on PROMs after primary corticoid injection for triggerfinger with a comparison of two different injection techniques.

详细描述

This study aims to compare two different methods of corticosteroid injections in patients with triggerfinger, and to study the effects of these injections by day-to-day self-assessment by the included study persons for four weeks. The patient assess: 1. Pain 2. Motion and 3. Triggering by VAS scale every day for four weeks.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Triggering of one or more fingers and/or impaired active finger motion and/or pain during active finger motion
  • Localized tenderness volar to the MCP joint of the affected finger
  • The patient seeks treatment

排除标准

  • Previous treatment for triggerfinger in the finger to be treated
  • Impaired function of finger due to previous trauma/infection or other condition
  • Suspicion of other cause than triggeriinger/tendovaginitis
  • Patient not able to follow instructions

研究组 & 干预措施

proximal phalangeal level

Experimental

injection in the the tendon sheet over proximal phalanx of finger

干预措施: Proximal phalangeal level (Procedure)

volar MCP level

Active Comparator

injection above the A1 pulley volar to the MCP joint

干预措施: Volar to the MCP-joint (Drug)

结局指标

主要结局

Impairment of finger motion

时间窗: Four weeks

Visual analouge scale (VAS), range 0-10, where 0 indicates "no impairment" and 10 "maximum impairment"

Triggering

时间窗: Four weeks

Visual analouge scale (VAS), range 0-10, where 0 indicates "no trigger phenomenon" and 10 "Trigger phenomenon all the time/ locked finger"

Pain after injection

时间窗: Four weeks

Visual analouge scale (VAS), range 0-10, where 0 indicates "no pain" and 10 "maximum pain"

次要结局

  • Quick-DASH(Four weeks)

研究者

发起方
Sahlgrenska University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Joakim Stromberg

Senior consultant surgeon, MD, PhD

Sahlgrenska University Hospital

研究点 (1)

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