Efficacy of laser in varicose insufficiency

Efficacy and side effects of Endovenous laser treatment for uncomplicated varicose veins: a randomized comparative study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201301118146N5

Enrollment

Registered

2013-01-26

Start date

2012-12-21

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Varicose veins of lower extremities. 183.9

Interventions

Intervention 1: laser ablation of saphenofemoral junction in varicose patient. Intervention 2: high ligation of saphenofemoral junction by surgical technique.

Treatment - Surgery

laser ablation of saphenofemoral junction in varicose patient

high ligation of saphenofemoral junction by surgical technique

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18 to 65 years; insufficiency of GSV and the Saphenofemoral junction (SFJ) with reflux at least up to the knee and symptoms of GSV insufficiency or CVI. Exclusion criteria: pregnancy; active malignancy; arterial occlusive disease with an Ankle Brachial Index of below 0.8; acute deep vein thrombosis (DVT); thrombophilia or high risk of pulmonary thromboemboli; history of inguinal surgery except for hernia and insufficiency of the lesser saphenous vein in the same limb requiring treatment. aim :compare Efficacy and side effects of Endovenous laser treatment for uncomplicated varicose vein

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Patency rate. Timepoint: 6months-12 month- 18 month. Method of measurement: Doppler Ultrasonography.;CEAP score. Timepoint: before treatment- 3 week-6 month-12 month-18 month. Method of measurement: physical exam.;AVVSS score. Timepoint: Before treatment -1week 3 month-6 month-12 month-18 month. Method of measurement: physical exam.	—

Secondary

Measure	Time frame
Pain. Timepoint: before treatment-1 week-3 month-6 month-12 month-18 month. Method of measurement: physical exam.;Edema. Timepoint: before treatment--1 week-3 month-6 month-12 month-18 month. Method of measurement: physical exam.;Pigmentation. Timepoint: before treatment -1 week- 3 month-6 month- 12 month- 18 month. Method of measurement: physical exam.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKhashayar Atqiaee

Shahid Beheshti University of Medical Sciences

khashayaratqiaee@gmail.com+98 21 8890 4546

Outcome results

None listed

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