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The efficacy and safety of picosecond 1064 nm Nd:YAG laser in treatment of post sclerotherapy hyperpigmentation: a pilot study.

The efficacy and safety of picosecond 1064 nm Nd:YAG laser in treatment of post sclerotherapy hyperpigmentation: a pilot study.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210507005
Enrollment
12
Registered
2021-05-07
Start date
2019-03-05
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

post sclerotherapy hyperpigmentation the complication of cosmetic sclerotherapy safety profile of using picosecond 1064 nm Nd:YAG laser in low-fluence non-ablative setting sclerotherapy hyperpigmentation laser sclerotherapy adverse effects

Interventions

We use picosecond 1064 nm Nd:YAG laser to treat the post-sclerotherapy hyper pigmented areas. The skin will be prepared by 70% alcohol solution before the procedure. . The indicated setting and para
Experimental Device
Picosecond 1064 nm Nd:YAG laser

Sponsors

Institute of Dermatology, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patient is diagnosed as post-sclerotherapy hyperpigmentation from sclerotherapy using 0.1- 1% polidocanol in liquid or foam solution. Off- treatment time is 3-months period. 2. No truncal reflux by Duplex ultrasound study. 3. The patient has 2 lesions or more. 4. Those lesions has similar melanin index. 5. Age > 18 years. 6. Fitzpatrick skin type III-V 7. Patient could make a visit as appointed 8. Patient has no history of using bleaching agents such as hydroquinone, retinoids prior to the study.

Exclusion criteria

Exclusion criteria: 1. Patient is receiving anticoagulant, minocycline or iron supplements. 2. Patient has received laser treatment on the study sites within 6 months. 3. Pregnant patient 4. Patient with history of photosensitive conditions 5. Patient with history or risk of keloidal scar formation

Design outcomes

Primary

MeasureTime frame
Mean melanin index at 4 weeks and 8 weeks after the intervention Mexameter

Secondary

MeasureTime frame
Patient satisfactory score 4 weeks after the intervention Patient reported outcome using a 5-point rating scale questionnaire.,Physician evaluation score 4 weeks after the intervention Physician reported outcome using a 5-point rating scale questionnaire.

Countries

Thailand

Contacts

Public ContactTanongkiet Tienthavorn

Institute of Dermatology

pic062@gmail.com0949366465

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026