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临床试验/NCT05383469
NCT05383469已完成不适用

Comparison of the Efficacy of Active Versus Passive Methods in Patients With Chronic Venous Insufficiency

Istanbul University - Cerrahpasa (IUC)2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2022年9月13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
66
试验地点
2
主要终点
Circumference measurements

研究概览

简要总结

The aim of our study was to compare the effectiveness of active and passive practices in patients with CVI.

详细描述

Volunteers who have been diagnosed with venous insufficiency according to the criteria of inclusion, who applied to Cardiovascular Surgery Department will be included this study.

Participants will be randomly allocated 3 groups using the 'Research Randomizer' website. In all groups, a common evaluation protocol will be applied to the patients.

Compression therapy will be applied to the first group. Active treatment in addition to compression therapy will be applied to the second group. Passive treatment in addition to compression therapy will be applied to the third group.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of venous insufficiency with duplex ultrasonography
  • Classification of CEAP (Clinical-Etiological-Anatomical-Pathological) used in venous insufficiency is C3-C4-C5-C6
  • Ankle-brachial index (ABI) is less than 0.7
  • Possibility to communicate in written and verbal in Turkish
  • Have a level of cognitive ability to understand the instructions given

排除标准

  • Presence of deep vein thrombosis
  • Ulceration or open burn wound in lower extremity greater than 4 cm
  • Presence of infected ulceration
  • Cardiorespiratory insufficiency
  • Orthopedic, rheumatologic or neurological comorbidities restrain the exercise in the lower extremity
  • Presence of a psychiatric illness requiring the use of prescribed medicines

结局指标

主要结局

Circumference measurements

时间窗: Change from Baseline circumferences at 8 weeks.

Circumference measurements will be recorded at 4 cm intervals to evaluated to edema.

次要结局

  • 6-Minute Walking Test(Assessment will be performed at baseline and at 8 weeks.)
  • Visual Analogue Scale (VAS)(Assessment will be performed at baseline and at 8 weeks.)
  • Handheld Dynamometer(Assessment will be performed at baseline and at 8 weeks.)
  • Chronic Venous Disease Quality of Life Questionnaire (CIVIQ) 20(Assessment will be performed at baseline and at 8 weeks.)
  • Venous Clinical Severity Score (VCSS)(Assessment will be performed tat baseline and at 8 weeks.)
  • 10-Meter Walking Test(Assessment will be performed at baseline and at 8 weeks.)

研究者

发起方
Istanbul University - Cerrahpasa (IUC)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Saliha Gürdal Karakelle

Research .Assistant

Istanbul University - Cerrahpasa (IUC)

研究点 (2)

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