Varicose Veins

9

Review clinical trials related to Varicose Veins. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

THRomboprophylaxis in Individuals Undergoing Superficial endoVEnous Treatment (THRIVE)

Endovenous interventions are keyhole operations for varicose veins that are carried out from within the vein itself. Varicose veins are enlarged veins close to the surface of the skin. They are connected to the bigger deeper veins in the leg (known as deep veins). Because of this, operations to close the varicose veins can increase the chance of a blood clot forming in the deep veins. Blood clots in the deep veins happen in around 1 in 50 people after endovenous operations. A clot in the leg can cause swelling, pain, and other long-term problems. If a clot in the leg breaks off and travels to the lungs, it can cause problems with the lung' ability to move oxygen from the air into the blood and may, in rare cases, be life threatening. Varicose vein procedures may carry a slightly higher risk of blood clot formation, and we are currently unsure if current clot reducing medicines are beneficial in preventing blood clots in people having varicose vein procedures. This study will investigate if it is worthwhile prescribing medicines to reduce blood clots after varicose vein procedures.

Participants needed: 3,175
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Imperial College LondonUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Adults (>18 years) [+2]

Clinical indication for therapeutic anticoagulation e.g., atrial fibrillation [+12]

Status: Recruiting

Research on the Application of Nursing Intervention Based on ITHBC Theory in Postoperative Self-Management of Patients With Varicose Veins of the Lower Extremities

This study constructed a postoperative self-management nursing intervention program for VVLE patients based on the ITHBC theory, and explored the impact of this program on the patients' postoperative self-management ability, self-efficacy, complication rate and quality of life.

Participants needed: 104
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Second Affiliated Hospital of Nanchang UniversityUpdated: May 6, 2026Locations: 1
Eligibility criteria

It meets the diagnostic criteria for varicose veins of the lower extremities in... [+4]

Secondary varicose veins of the lower extremities ; [+3]

Status: Recruiting

Polidocanol Foam With or Without Transdermal Laser in Varicose Veins

This randomized, parallel clinical trial with blinded outcome assessment will compare the clinical and aesthetic outcomes of polidocanol foam sclerotherapy alone versus polidocanol foam associated with long-pulse 1064 nm Nd:YAG transdermal laser in the treatment of lower-limb tributary varicose veins. The primary endpoint is venous occlusion rate at 30 days, assessed by Doppler ultrasound. Secondary outcomes include cutaneous hyperpigmentation, pain, patient satisfaction, and adverse events.

Participants needed: 102
Trial details
Age: 21-75Biological sex: AllType: InterventionalSponsor: Hospital Universitario Pedro ErnestoUpdated: May 5, 2026Locations: 1
Eligibility criteria

Age 21 to 75 years [+7]

CEAP clinical class ≥ 4 [+12]

Status: Recruiting

Study on Treatment of Varicose Veins by Endovenous Laser (1940 nm vs 1470 nm)

The goal of this clinical trial is to compare efficacy of two wavelength for EndoVenous Laser Ablation (EVLA) in treatment of varicose veins of the lower limbs. The main questions it aims to answers are : 1. Is the increase of wavelength form 1470 nm to 1940 nm affect the efficacy of varicose veins treatment ? 2. Is the increase of wavelength reduce complication or pain ? Participants are patients with varicose veins of lower limbs and candidate for endovenous laser ablation. After laser ablation patients will be followed during 5 years for clinical evaluation, recording potential treatment complications and quality of life evaluation. Researchers will compare strategy 1(EVLA with an endovenous laser at 1940 nm) vs strategy 2 (EVLA with an endovenous laser at 1470 nm) in varicose veins treatment to see if efficacy of treatment is not reduce, and to see if complications of EVLA treatment can be reduced.

Participants needed: 280
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Clinique PasteurUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Primary insufficiency of the great saphenous vein (GSV) and/or small saphenous v... [+5]

Patient with a current serious pathology and/or a life expectancy of less than 5... [+10]

Status: Recruiting

The Influence of Laser Crossectomy With Different Wavelengths on Varicose Vein Progression

Technically successful laser crossectomy will reduce the risk of reflux recurrence at the sapheno-femoral junction without increasing the risk of endovenous heat-induced thrombosis, which may positively impact the likelihood of ultrasound- or clinical-recurrence of varicose veins. Similar technical efficacy is expected for laser crossectomy at 1940 nm and 1470 nm. A possible advantage of the 1940 nm wavelength in terms of postoperative pain intensity and the risk of adverse events cannot be ruled out.

Participants needed: 400
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Pirogov Russian National Research Medical UniversityUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Age >18 years [+4]

Primary reflux outside the GSV trunk (including combined reflux) [+8]

Status: Recruiting

Caprini Score in Venous Surgery: a Prospective Cohort Study

The aim of the study is to make a validation of Caprini score in patients undergoing varicose veins surgery, especially endovascular procedures (endovascular laser treatment - EVLT, radiofrequency ablation - RFA, ultrasound-guided foam sclerotherapy - USFS) and to identify patients with elevated risk of postoperative venous thromboembolism (VTE) who will benefit from prophylactic anticoagulation.

Participants needed: 3,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Pirogov Russian National Research Medical UniversityUpdated: Mar 2, 2026Locations: 1
Eligibility criteria

age over 18 years [+3]

Status: Recruiting

Vacuum-assisted Laser Ablation (VALA) for Treatment of Large Saphenous Veins

Endovenous thermal ablation (EVTA), including radiofrequency ablation (RFA) and endovenous laser ablation (EVLA), is considered the main method for the treatment of symptomatic truncal vein reflux. However, there are controversial data concerning their efficacy and safety in ablating large saphenous veins because of high risk of heat-induced thrombosis (EHIT), incomplete ablation and recanalization.1-5 The use of vacuum evacuation of the remaining intraluminal blood during endovenous laser ablation allows to decrease the risk of intraoperative (carbonization and destruction of the fiber lens) and postoperative complications (EHIT, hyperpigmentation, "string" feeling) and leads to reduction of recovery because of short period of vein resorption. The aim of the study is to evaluate the safety and effectiveness of endovenous thermal ablation with or without vacuum evacuation for the treatment of incompetent large saphenous veins (\>15 mm).

Participants needed: 184
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Center Of PhlebologyUpdated: May 14, 2025Locations: 9
Eligibility criteria

Age over 18 years [+2]

pregnancy or lactation [+10]

Status: Not yet recruiting

Evaluating QoL and Postoperative Complications Using TEThA Technique in the Treatment of Tributary Veins

Endovenous laser thermoablation is a well-established alternative for the treatment of tributary veins. We believe that it is possible to improve the techniques described in the literature, aiming not only to allocate the laser fiber within the venous lumen, but mainly to transfix the vessel walls - a technique called TEThA (Transfixing Endovenous Thermal Ablation).

Participants needed: 20
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Nara Medeiros Cunha de Melo VasconcelosUpdated: Nov 1, 2024
Eligibility criteria

Not listed

Status: Recruiting

Study of Foam Sclerotherapy Versus Ambulatory Phlebectomy

This study will be comparing the treatment of varicose vein tributaries using either foam sclerotherapy or ambulatory phlebectomies. Patients will be randomised to having either ambulatory phlebectomy (group A) or foam sclerotherapy (group B) following treatment of their saphenous vein. The re-intervention rates, safety, patient experience as well as the cost effectiveness of each intervention will be assessed.

Participants needed: 160
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Imperial College LondonUpdated: Jul 5, 2024Locations: 1
Eligibility criteria

Adults over 18 years of age [+2]

Current DVT [+8]