Endovenous Radiofrequency Ablation Closure System in the Treatment of Varicose Veins

Varicose Veins Clinical Trial

Official title:

Prospective, Multi-center, Randomized Controlled Study to Evaluate the Effectiveness and Safety of Endovenous Radiofrequency Ablation Closure System in the Treatment of Varicose Veins

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04671641
• Other study ID #: RFS 1.0
• Status: Active, not recruiting
• Phase: N/A
• Start date: April 1, 2021
• Est. completion date: October 2, 2022

Study information

• Verified date: September 2021
• Source: Suzhou Hengruihongyuan Medical Technology Co. LTD
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to evaluate the effectiveness and safety of the endovenous radiofrequency ablation closure system produced by Suzhou Hengrui Hongyuan Medical Technology Co., Ltd. for the treatment of varicose veins.

Description:

In this prospective, multi-center, randomized controlled study, 176 patients who were diagnosed with varicose veins and met the inclusion criteria without any exclusion criteria were randomly divided into the experimental group (Hongyuan Endovenous Radiofrequency Ablation Closure System)and control group (Medtronic's ClosureFast™ Radiofrequency Ablation System) at 1:1. The effectiveness of the product was evaluated by the vascular closure rate at 6 months after the operation, and the safety of the product was evaluated by the incidence of adverse events and serious adverse events within 6 months after the operation.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 176
• Est. completion date: October 2, 2022
• Est. primary completion date: July 2, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Age 18-80 years old, no gender limit.

2. Great saphenous varicose, CEAP grade C2-C6.

3. The diameter of the diseased vein is =2mm, =15mm.

4. Expected survival period = 6 months.

5. The informed consent form can be signed by the patient or the legal representative.

Exclusion Criteria:

1. Are pregnant or breastfeeding.

2. Participating in clinical trials of other devices or drugs.

3. Deep vein thrombosis in the affected limb.

4. Uncorrectable coagulation dysfunction and obvious abnormal blood picture, with obvious bleeding tendency (platelets=30x109/L).

5. Acute thrombosis in the main saphenous vein of the affected limb.

6. The investigator judged that it is not suitable to participate in the clinical trial.

Related Conditions & MeSH terms

• Varicose Veins

Intervention

Device:
• radiofrequency ablation
ultrasound-guided radiofrequency ablation is performed to treat varicose veins patients

Locations

Country	Name	City	State
China	Affiliated Hangzhou First People's Hospital ,Zhejiang University School of Medicine	Hangzhou	Zhejiang
China	The Fourth Affiliated Hospital ,Zhejiang University School of Medicine	Hangzhou	Zhejiang
China	The Second Affiliated Hospital of Zhejiang University School of Medicine	Hangzhou	Zhejiang
China	ZheJiang Provincial People's Hospital	Hangzhou	Zhejiang
China	Zhongshan Hospital	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Suzhou Hengruihongyuan Medical Technology Co. LTD

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Rate of serious adverse events within 6 months after surgery		6 months
Other	Rate of adverse events within 6 months after surgery		6 months
Primary	Vascular closure rate at 6 months after the operation	Calculation method: completely closed patients / total cases of subjects in the same group x 100%.; Definition of complete closure: Complete closure refers to ultrasound follow-up at 6 months after surgery that shows no blood flow in varicose veins.	6 months
Secondary	CEAP	The CEAP is an elaborate scoring system for varicose veins and other disorders from venous insufficiency. It has been developed to determine the severity of the condition for diagnosis and treatment point of view. CEAP stands for: Clinical Etiopathological Anatomical Pathophysiological	6 months
Secondary	Technical success rate	The device is delivered in place and withdrawn smoothly, and the target diseased blood vessel is immediately examined by ultrasound without blood flow.	6 months
Secondary	Evaluation of the use of devices	For endovenous radiofrequency closure catheter: evaluation on the degree of device flexibility, crossability, accuracy, usability (subjective evaluation scale: excellent, good and poor) For endovenous radiofrequency closure generator: evaluation on applicability,accuracy of identifying catheter version, stability in the procedure(subjective evaluation: yes or no)	6 months
Secondary	VCSS	Changes from baseline in venous clinical severity score (VCSS) (0-30, higher scores mean a worse outcome) in outpatient services. the VCSS was derived by the American Venous Forum from the CEAP classification and provides means by which clinical outcomes in venous disease can be monitored in time.Compared to the CEAP, VCSS is said to be more responsive to changes in disease severity, thus making it great for progressive rankings. It proved good inter and intra observer reproducibility and is often cited in quality of life assessments	6 months