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临床试验/NCT05914740
NCT05914740招募中不适用

Feasibility Study of Ultrasound-guided Functional Remodeling of Lower Extremity Superficial Venous Valve

The Fourth Affiliated Hospital of Zhejiang University School of Medicine1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2023年4月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
10
试验地点
1
主要终点
Changes in the duration of venous valve regurgitation

研究概览

简要总结

In this project, an exploratory study was conducted to perform in situ venous valve remodeling in vivo, evaluate venous valve function after surgery and conduct regular follow-up, collect relevant ultrasonic data before, during and after surgery, and evaluate the safety and effectiveness of Ultrasound-guided percutaneous great saphenous vein valve functional remodeling.

详细描述

A certain number of patients meeting the requirements (meeting the inclusion criteria, but not meeting the exclusion criteria) were selected for preoperative hemodynamic evaluation of lower extremity vein ultrasound to determine the reflux points and reflux points, identify the blood circulation pattern, and design an individualized surgical program. Intraoperative venous valve was remodeled in situ under ultrasound guidance. Postoperative ultrasound was used to assess venous valve function and complications in the operative area.

Screening period (before surgery 14 days to 0 days) Subject signs informed consent. General information and previous medical history of subjects were collected, preoperative laboratory examination (blood routine, blood biochemistry, coagulation function, preoperative immunity, blood type), electrocardiogram, ultrasound, preoperative hemodynamic evaluation of lower extremity vein were completed, and evaluation scales such as CEAP grading, VCSS, AVVQ, CIVIQ and pain score were completed.

Subjects who meet the inclusion criteria and do not meet all exclusion criteria will be admitted.

Day of surgery (day 0) Preoperative ultrasound was re-evaluated to confirm the valve function, and the tissue was disinfected. Hyaluronic acid was injected around the valve of the great saphenous vein to rebuild the valve about 1-2ml, and the whole process was monitored under ultrasound. During the injection, the valve function was pumped back for protection, and the injection was performed multiple times at different points. Supplementary injection: Following the subject's voluntary principle, the researcher can give supplementary injection after evaluating the general condition of the subject.

The follow-up period for each subject was 12 months ±20 days after enrollment. Follow-up period (±3 days at 1 week, ±5 days at 1 month, ±10 days at 3 months, ±15 days at 6 months, ±20 days at 1 year) General data of subjects were collected, laboratory examination (blood routine and blood biochemistry) and postoperative ultrasound hemodynamic evaluation of lower limb veins were improved, and evaluation scales such as VCSS, AVVQ, CIVIQ and pain score were completed.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

盲法说明

Open trial

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 18-80, gender unlimited
  • •CEAP grading was C2-C5 patients
  • •The patient was clinically diagnosed as a primary varicose great saphenous vein of lower extremity, and the ultrasound findings were great saphenous vein valve insufficiency (complete structure, normal shape, enlarged valve ring, Duration of reflux >0.5s), only unilateral varicose great saphenous vein was treated this time

排除标准

  • •Patients with target vessel diameter < 3mm
  • •The final valve of the great saphenous vein was not clear or lost its normal shape on ultrasound
  • •Patients with deep vein valvular insufficiency
  • •The presence of thrombus or thrombophlebitis in the main trunk of great cryptic skin
  • •Target diseased blood vessel had previously received surgical treatment
  • •Patients with deep vein thrombosis or history of pulmonary distension embolism
  • •Patients with active implants such as pacemakers or ICDs
  • •Patients with severe abnormal liver and kidney function (more than three times the normal value)
  • •Patients with non-primary varicose veins caused by post-deep vein thrombosis syndrome, Cockett syndrome (iliac vein compression syndrome), KT syndrome (venous malformation hypertrophy syndrome >, arteriovenous sputum, etc
  • •Any serious or uncontrolled systemic disease (including poorly medicated hypertension, diabetes, and diseases with active bleeding signs or severe coagulopathy)
  • •Patients with diseases that may make treatment and evaluation difficult (e.g., malignant arsine tumor, acute infectious diseases, sepsis, systemic intolerability of surgery, life expectancy less than 12 months, etc.)
  • •Pregnant and lactating women, or those who planned to have children during the study period
  • •Patients who have participated in clinical trials of other drugs or medical devices within the last 3 months
  • •Anesthetist and other patients were deemed unsuitable for the study

研究组 & 干预措施

Venous valve remodeling

Experimental

Venous valve function was remodeled under ultrasound guidance

干预措施: Ultrasound guided functional remodeling of lower extremity superficial vein valve (Procedure)

结局指标

主要结局

Changes in the duration of venous valve regurgitation

时间窗: 1 year after intervention

The duration of venous valve regurgitation was measured under calf compression test

Venous valve regurgitation or not

时间窗: 1 year after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Venous valve regurgitation or not

时间窗: immediately after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Venous valve regurgitation or not

时间窗: 1 week after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Venous valve regurgitation or not

时间窗: 1 month after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Venous valve regurgitation or not

时间窗: 3 months after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Venous valve regurgitation or not

时间窗: 6 months after intervention

Under the calf compression test, the venous valves were observed for blood flow regurgitation signal

Changes in the duration of venous valve regurgitation

时间窗: immediately after intervention

The duration of venous valve regurgitation was measured under calf compression test

Changes in the duration of venous valve regurgitation

时间窗: 1 week after intervention

The duration of venous valve regurgitation was measured under calf compression test

Changes in the duration of venous valve regurgitation

时间窗: 1 month after intervention

The duration of venous valve regurgitation was measured under calf compression test

Changes in the duration of venous valve regurgitation

时间窗: 3 months after intervention

The duration of venous valve regurgitation was measured under calf compression test

Changes in the duration of venous valve regurgitation

时间窗: 6 months after intervention

The duration of venous valve regurgitation was measured under calf compression test

次要结局

未报告次要终点

研究者

发起方
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
申办方类型
Other
责任方
Sponsor

研究点 (1)

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