Calcium Dobesilate After Radiofrequency Ablation for Varicose Veins
Starting soon · Phase 4
Conditions studied: Varicose Veins Leg, Great Saphenous Vein Insufficiency, Chronic Venous Insufficiency
In brief
This study evaluates whether calcium dobesilate, a venoactive drug, improves recovery after radiofrequency ablation (RFA) for varicose veins. Patients with great saphenous vein insufficiency undergoing RFA will be randomly assigned to receive either calcium dobesilate (500 mg twice daily) or standard care alone. The treatment starts 7 days before the procedure and continues for 30 days after. The primary outcome is postoperative pain at day 7. Secondary outcomes include pain at days 14 and 30, quality of life, ecchymosis, and return to daily activities.
Key facts
- Study ID
- NCT07390097
- Run by
- Oguz Arslanturk
- People needed
- 250
- Starts
- 2026-02-28
- Expected to finish
- 2026-11-01
- Last updated by the study team
- 2026-02-05
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-70 years
- Symptomatic primary varicose veins (CEAP classification C2-C4)
- Great saphenous vein insufficiency confirmed by duplex ultrasound (reflux >0.5 seconds)
- Great saphenous vein diameter 5-12 mm
- Scheduled for radiofrequency ablation
- Able to provide written informed consent
You may not qualify if…
- History of deep vein thrombosis
- Peripheral arterial disease (ABI <0.9)
- Active venous ulcer (CEAP C6)
- Pregnancy or breastfeeding
- Severe renal or hepatic insufficiency
- Known allergy to calcium dobesilate
- Use of venoactive drugs within the past 4 weeks
- Current anticoagulant therapy
- Previous venous intervention on the same limb
- Bilateral disease requiring simultaneous treatment
- Inability to comply with follow-up schedule
Where it is running
- Zonguldak Bulent Ecevit University Hospital, Department of Cardiovascular Surgery — Kozlu, Zonguldak Province, Turkey (Türkiye)
Full record on ClinicalTrials.gov
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