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临床试验/NCT06207045
NCT06207045尚未招募不适用

The Effects of Limb Elevation During Gout Flare Episodes : A Pilot, Randomised Controlled Trial

Thammasat University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
试验地点
2
主要终点
Reduction of pain score

研究概览

简要总结

The goal of this open-label randomized controlled trial is to explore the benefit of limb elevation in inpatient gout flare episodes, compared with standard treatment The main questions are;

  • Is limb elevation able to reduce pain during gout flare episodes to a greater degree compared with standard treatment ?
  • Is Is limb elevation able to reduce joint swelling during gout flare episodes to a greater degree compared with standard treatment ?

Participants will be divided into 2 group;

  1. Limb elevation group
  2. control group All participants will receive standard medical therapy consisting of colchicine 0.6 mg per day plus prednisolone 30 mg per day for 2 days

Pain score and joint circumference will be recored at recruitment, 24 hour and 48 hour

详细描述

Limb elevation has shown benefit in ankle sprain and venous insufficiency, but its benefit has not been studied in people with gout flare. In this open-label randomized controlled trial, 30 adults diagnosed with gout flare during their hospitalization will be randomized to receive limb elevation plus standard medication for gout flare (limb elevation group) or standard medication only (control group). Primary outcome is reduction in 10-point visual analogue scale for pain at 48 hours after enrollment and the secondary outcome is the reduction of the circumference of affected joint at 48 hours after enrollment. Comparison of pain score and joint circumference reduction will be made using Wilcoxon Rank-sum test. Our study results may provide some evidence in support of limb elevation as a supplementary non-pharmacological therapy for relief of gout flare.

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

  • Aged ≥ 18 years
  • Diagnosis of Gout according to 2015 The ACR/EULAR gout classification criteria

排除标准

  • Receive Non-Steroidal Anti-inflammatory Drugs or Intra-articular corticosteroids or prednisolone > 10 mg within 24 hours before enrollment
  • Unstable vital sign
  • Receiving joint aspiration for release joint effusion ≥ 10 ml after enrollment
  • Gout flares involve axial joints e.g. hip
  • Glomerular Filtration Rates < 30 ml/min/1.73m2
  • Communication problems

结局指标

主要结局

Reduction of pain score

时间窗: 48 hours

10-points Visual Analogue Scale

次要结局

  • Joint circumference(48 hours)

研究者

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

saitip sangkamanovet

Dr.

Thammasat University

研究点 (2)

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