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NCT Number: NCT07678697

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.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams University

Cairo, 11591, Egypt

Location status: Recruiting

Location contact

Ahmed G Abdellattif, MD

PRINCIPAL_INVESTIGATOR

Mina G Basta, MD

PRINCIPAL_INVESTIGATOR

Mohamed A Hagag, MD

CONTACT

[email protected]

00201126560324

About this study

Reticular veins and telangiectasias (spider veins) represent common chronic venous disorders affecting a large proportion of the adult population, particularly women.

The Cryo-Laser and Cryo-Sclerotherapy (CLaCS) technique has emerged as an innovative method combining transdermal laser therapy, injection sclerotherapy, and skin cooling. This multimodal approach enhances visualization of feeder veins using augmented reality or vein illumination systems, allowing precise targeting and improved clearance rates. Cooling reduces pain and protects the epidermis, making the procedure more tolerable and safer.

Nd:YAG laser (1064 nm) is considered the cornerstone of the CLaCS technique due to its deeper penetration and selective photothermolysis of hemoglobin. It effectively targets deeper reticular veins (up to 3-4 mm depth), induces vessel wall contraction, and facilitates subsequent sclerotherapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 18-60 years.
  • Both sexes.
  • Presence of reticular veins and/or telangiectasias (CEAP classification C1).
  • Fitzpatrick skin types II-V.
  • Patients seeking cosmetic treatment.

Exclusion criteria

  • Pregnancy or lactation.
  • History of deep vein thrombosis.
  • Coagulation disorders.
  • Allergy to sclerosant agents.
  • Active skin infection at treatment site.
  • Previous treatment of target veins within 6 months.
  • Great saphenous vein or short saphenous vein incompetence.
  • Deep venous insufficiency or thrombosis.
  • Abnormal venous duplex findings.

Treatment and study plan

Nd:Yag Laser

Device

Patients will receive Nd:YAG laser (1064 nm) + injection sclerotherapy (CLaCS).

diode laser

Drug

Patients will receive Diode laser (980 nm) + injection sclerotherapy (CLaCS).

Primary outcomes

  1. Degree of vein clearance

    Time frame: 6 months postoperatively

    Degree of vein clearance will be assessed by immediate endpoint response during laser application, defined as either instantaneous disappearance of the vein or an immediate change in vein color.

Secondary outcomes

  1. Degree of pain

    Time frame: 6 months postoperatively

    Each patient will be instructed about postoperative pain assessment with VAS. VAS (0 represents "no pain" while 10 represents "the worst pain imaginable").

  2. Degree of patient satisfaction

    Time frame: 6 months postoperatively

    Degree of patient satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied; 5, extremely satisfied).

  3. Incidence of complications

    Time frame: 6 months postoperatively

    Incidence of complications such as hyperpigmentation, burns, and matting will be recorded.

  4. Number of treatment sessions required

    Time frame: 6 months postoperatively

    Number of treatment sessions required will be recorded.

  5. Recurrence rate

    Time frame: 6 months postoperatively

    Recurrence rate will be recorded.

Study contacts

Contact information is provided by the study sponsor or research team.

Mohamed A Hagag, MD

CONTACT

[email protected]

00201126560324

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 1, 2026
Registry last updated
Jul 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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