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The efficacy and safety of no thromboprophylaxis after endovenous radiofrequency ablation (TRAIN): a randomized controlled, non-interiority trial

The efficacy and safety of no thromboprophylaxis after endovenous radiofrequency ablation (TRAIN): a randomized controlled, non-interiority trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081638
Enrollment
Unknown
Registered
2024-03-07
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

venous diseas

Interventions

Control group:Participants with great saphenous varicose veins underwent endovascular thermal ablation followed by prophylactic anticoagulation
Experimental group:Participants with great saphenous varicose veins who underwent endovascular thermal ablation without prophylactic anticoagulation

Sponsors

Department of Vascular Surgery, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Male or non-pregnant female subjects, aged 18 years or older, with a life expectancy sufficient to complete all study procedures 2) patients with deep venous insufficiency of lower extremities and superficial varicose veins indicated by preoperative color Doppler ultrasound 3) Preoperative examination showed that the patient had no iliac vein compression 4) patients voluntarily participated in the study 5) Informed consent approved by the ethics committee

Exclusion criteria

Exclusion criteria: 1) patients with atrial fibrillation or valvular heart disease requiring regular anticoagulation 2) known hypersensitivity to sclerosing agents 3) history of myocardial infarction, thrombolytic therapy, or angina within 2 weeks before enrollment 4) stroke or TIA within 3 months before surgery 5) Stage C6 venous leg ulcer 6) patients with preoperative lower extremity venous thrombosis 7) Complicated with foramen ovale may not be the case

Design outcomes

Primary

MeasureTime frame
Thrombosis-related events ;

Secondary

MeasureTime frame
Ecchymosis of limbs;Induration and hematoma of limbs;The incision was infected, red and swollen, and healed poorly;

Countries

China

Contacts

Public ContactDing Yuan

+86 189 8060 6344

yuanding@wchscu.cn+86 189 8060 6344

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026