跳至主要内容
临床试验/NCT03683095
NCT03683095撤回不适用

Efficacy of Lymphovenous Bypass in the Treatment of Extremity Lymphedema

Ottawa Hospital Research Institute0 个研究点开始时间: 2023年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Extremity volume (v)

研究概览

简要总结

BACKGROUND: Lymphedema is a pathologic soft tissue swelling that arises secondary to disruption of the lymphatic system. Lymphedema affects approximately 250 million people worldwide and causes significant physical and psychological morbidity. There is no definitive treatment for lymphedema. Lymphovenous bypass - microsurgically anastomosing lymphatic channels and venules - has demonstrated promising results in the treatment of lymphedema. PURPOSE: The purpose of this study is to determine the efficacy of lymphovenous bypass in treating extremity lymphedema. METHODS: This is a prospective, single-arm, cohort study. Eligible patients between 18-70 years of age with extremity lymphedema will undergo lymphovenous bypass. The primary outcome measure will be extremity volume and the secondary outcome measure will be quality of life assessed by a validated assessment tool for lymphedema of the limbs (LYMQOL). Patients will be assessed preoperatively and at 3, 6, 9, and 12-months postoperatively. Each participant will serve as their own control.

Primary and secondary outcome measures will be assessed with paired t-tests. With a sample size of 9 patients we will have at least 80% power to reject the null hypothesis assuming an alpha level of 0.01. To further increase the power and to account for patients lost to follow-up the investigators will target a patient recruitment of 20.

The findings of this study will help further elucidate the role of lymphovenous bypass in the treatment of extremity lymphedema.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-70 years.
  • Lymphedema of the upper or lower extremity.
  • International Society of Lymphology Stage I-II.

排除标准

  • Significant comorbidities that would preclude a patient from receiving a general anesthetic.

结局指标

主要结局

Extremity volume (v)

时间窗: Assessed preoperatively and 12-months postoperatively.

Extremity volume will be calculated using the truncated cone formula based on limb circumference measurements.

次要结局

  • Quality of life assessment tool for lymphedema of the limbs (LYMQOL).(Assessed preoperatively and 12-months postoperatively.)

研究者

申办方类型
Other
责任方
Sponsor

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