Reticular Veins

2

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

Condition / disease
Location
Status: Recruiting

Foam Sclerotherapy With or Without Transdermal Laser for Reticular Veins and Telangiectasias

This prospective, randomized, controlled, intraindividual split-leg clinical trial will compare isolated polidocanol foam sclerotherapy with the Cryo-Laser After Foam (CLaF) technique for the treatment of reticular veins and telangiectasias of the lower limbs. The study will include 70 women aged 18 to 60 years with bilateral CEAP C1 telangiectasias and/or reticular veins. Each participant will receive CLaF in one lower limb and isolated foam sclerotherapy in the contralateral limb, with treatment laterality determined by randomization. The CLaF technique consists of polidocanol foam sclerotherapy followed immediately by transdermal 1064-nm Nd:YAG laser under continuous cold-air cooling. The study will evaluate vascular clearance, residual vascular area, hyperpigmentation, retained thrombi and need for drainage, pain, adverse events, aesthetic improvement, patient satisfaction, and quality of life during follow-up through 180 days.

Participants needed: 70
Trial details
Phase: Phase 4Age: 18-60Biological sex: FemaleType: InterventionalSponsor: University of Sao PauloUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Female participants aged 18 to 60 years. [+6]

Saphenous or perforator venous reflux. [+11]

Status: Recruiting

Nd:YAG Laser Combined With Injection Sclerotherapy Versus Diode Laser in the Treatment of Reticular Veins and Telangiectasias Using CLaCS Technique

This study aims to compare the efficacy (in terms of vein clearance) and safety of Nd:YAG laser combined with injection sclerotherapy versus diode laser combined with injection sclerotherapy in the treatment of reticular veins and telangiectasias using the Cryo-Laser and Cryo-Sclerotherapy (CLaCS) technique.

Participants needed: 80
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Ain Shams UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Patients aged 18-60 years. [+4]

Pregnancy or lactation. [+8]