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临床试验/NCT06730789
NCT06730789已完成不适用

Prospective Comparison of Conservative Treatment Methods in Patients With Lateral Epicondylitis

Uludag University2 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2020年12月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
54
试验地点
2
主要终点
Visual analog score

研究概览

简要总结

Conservative treatments follow the vast majority of treatments in lateral epicondylitis. In this research, we aimed to elucidate the treatment outcomes of patients via epicondylitis bandage, wrist dorsiflexion splint, and kinesio tape groups by sequential randomization and to compare treatment outcomes.

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

  • Patients who were ≥18 years of age, and had no history of elbow surgery.
  • Participants should have pain and sensitivity, with symptom duration less than 12 weeks.
  • Patients with a positive result in one of the provocation tests (Maudsley's Test-resisted middle finger extension extensor carpi radialis test), resisted wrist extension, or passive stretching of the wrist extensors (Mill's Test) were included.

排除标准

  • Patients under 18 years of age,
  • patients who did not consent to participate in the study,
  • those who had previous surgery on the elbow,
  • presence of cervical spondylosis and radiculopathy,
  • presence of endocrine disease,
  • presence of autoimmune disease,
  • presence of concomitant entrapment neuropathy or polyneuropathy,
  • pregnancy,
  • presence of systemic inflammatory disease,
  • presence of acute trauma,
  • presence of deformity in the upper extremity,
  • presence of metabolic disease,
  • presence of elbow arthritis,
  • presence of allergy to kinesio tape and orthoses,
  • having received treatment for lateral epicondylitis in the past (exercise, injection, NSAIDs).

结局指标

主要结局

Visual analog score

时间窗: At sixth weeks.

Minimum value: 0 Maximum value:10 Minimum is better.

次要结局

  • Disabilities of the Arm, Shoulder Score(At sixth weeks.)

研究者

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

Yücel Bilgin

MD, Orthopedics and Traumatolody Specialist

Uludag University

研究点 (2)

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