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Comparing standard PICO second laser and combination of fractional and standard picosecond laser in the treatment of tattoo removal.

Safety and efficacy of standard PICO second laser alone and in combining with fractional picosecond laser in the treatment of tattoo removal - a prospective split study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077588
Enrollment
10
Registered
2024-12-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: L818- Other specified disorders of pigmentation

Interventions

Intervention1: combination of Fractional and standard picosecond laser: 4 mm spot size and fluence starting at 0.8-1J/cm2/1 pass + fractional picosecond laser will be done with 8mm spot size and flue

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: All Patients of age 18 to 60 years wants to remove unwanted tattoos Patients willing to participate in the study with their informed consent Patients not undergoing any other treatment for the same

Exclusion criteria

Exclusion criteria: Associated photoaggravated skin diseases and medical illness, for example, systemic lupus erythematosus. Treatment area with active cutaneous infections, for example, herpes labialis, staphylococcal infections. Unstable vitiligo and psoriasis for risk of Koebnerization of the treated area. Tattoo granuloma Patients with skin malignancy Pregnancy and Lactation women Bindi tattoo Have taken any treatment in the past for tattoo removal

Design outcomes

Primary

MeasureTime frame
1.To determine the efficacy of standard picosecond laser in the treatment of tattoo removal 3.Efficacy of the Fractional Picosecond laser and standard Picosecond laser in tattoo removalTimepoint: After 6 months

Secondary

MeasureTime frame
Physician global assessment (PGA) evaluation using four point scale with Grades of 1 minimal, 2 moderate, 3 marked and 4 near total improvement. Baseline and at weeks 6,12,18 and 24 weeksTimepoint: After 6 months

Countries

India

Contacts

Public ContactDr Chaithra Shenoy

CUTIS Academy of Cutaneous Sciences

chaithrashenoy@gmail.com9739247155

Outcome results

None listed

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