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临床试验/NCT06329219
NCT06329219Unknown不适用

Water-filtered Infrared-A Radiation in Patients With Hand Osteoarthritis - a Randomized Controlled Trial

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年3月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
70
试验地点
1
主要终点
Pain in the finger joints on visual analogue scale

研究概览

简要总结

The aim of this clinical trial is to evaluate the effects of water-filtered Infrared-A radiation on patients suffering from hand osteoarthritis. The main questions it aims to answer are:

  • Does water-filtered Infrared-A radiation reduce pain and improve the function of finger joints over time?
  • Are patients satisfied with the treatment results when compared to those who were on a wait-list?

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Diagnosis of finger polyarthritis (confirmed by a specialist, radiological findings available)
  • •Local pain for more than 50% of the day in the past 3 months.
  • •Subjective pain intensity of local pain in the last 24 hours on a VAS scale of 0 to 10 being >
  • •No planned local treatment in the next 6 months.
  • •No planned intra-articular injections within the next 6 months.
  • •The patient must be able to understand the study explanations and appropriately follow the instructions of the investigating physician.

排除标准

  • •Chronic inflammatory joint diseases.
  • •Poor general health.
  • •Febrile diseases.
  • •Fibromyalgia syndrome.
  • •Psychotic disorders.
  • •Severe comorbidities.
  • •Acute unclear skin diseases.
  • •Heat urticaria.
  • •Painful diseases/diagnoses of the shoulder and/or arm.
  • •Lymphatic vessel diseases (lymphedema, lymphangitis).
  • •Porphyria.
  • •Pain-associated diseases/diagnoses of the shoulder and/or arm.
  • •Intra-articular injections or arthroscopies within the last 3 months.
  • •Previous or planned surgical procedure on the affected joints in the last 8 weeks or in the upcoming 6 months.
  • •Intake or application of photosensitizing drugs or extracts (e.g., porphyrins, tetracyclines, sulfonamides, psoralenes, St. John's wort).
  • •Systemic medication with glucocorticoids or immunosuppressants.
  • •Pain medication with opioid analgesics.
  • •Known pregnancy.
  • •Concurrent participation in another clinical trial.

研究组 & 干预措施

Radiation

Experimental

Participants in the intervention group each receive a hyperthermia device for water-filtered Infrared-A radiation.

干预措施: water-filtered Infrared-A radiation (Device)

Waiting list

No Intervention

Participants in the control group initially receive no therapeutic intervention, but can receive it after the study's last visit for 3 months.

结局指标

主要结局

Pain in the finger joints on visual analogue scale

时间窗: Baseline, 12 weeks

Average pain in the finger joints over the last 7 days after 12 weeks compared to baseline on the Visual Analog Scale (VAS, 0-100mm) compared to the waiting list control group.

次要结局

  • Hand Dynamometer(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Disabilities of Arm, Shoulder and Hand (DASH) questionnaire(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Short Form (SF)-36 Health Survey (SF-36)(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Functional Index for Hand OsteoArthritis (FIHOA)(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Pain Self-Efficacy Questionnaire(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Pain medication (number per day)(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Hospital Anxiety and Depression Scale (HADS)(Baseline, 6 weeks, 12 weeks, 24 weeks)
  • Tolerability of the intervention(Baseline, 6 weeks, 12 weeks, 24 weeks)

研究者

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

Andreas Michalsen

Principal Investigator

Charite University, Berlin, Germany

研究点 (1)

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