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A comparative study to compare laser and injection therapy vs injection treatment alone in treating keloids.

A comparative study on the efficacy of intense pulse Light therapy combined with Intralesional steroids versus Intralesional steroids alone in the treatment of Keloids. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058276
Enrollment
50
Registered
2023-10-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: L918- Other hypertrophic disorders of the skin

Interventions

Intervention1: intense pulse light therapy and intralesional steroids: Intense pulse light(530nm and 640nm filter) topically and intralesional steroids (40mg/ml)subcutaneous maximum 6 sittings at 4 w

Sponsors

DrULavanya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All clinically diagnosed cases of keloid . Patients who are willing to give informed consent.

Exclusion criteria

Exclusion criteria: Before starting the study - Patients who are pregnant or lactating. Patients planning for pregnancy. Patients with history of intake of oral retinoids in the past 6 months. Patients with signs of active infection or lesions suspicious of malignancy. Patients with diseases or genetic conditions causing photosensitivity or tending to aggravate after light exposure. Patients with co-morbidities- DM,SHT,TB,CAD,EPILEPSY,BA. Patients on Photosensitizing drugs,immunosuppressive drugs,anti coagulants. Bleeding and coagulation disorders,HIV. During Study - If patient develops severe side effects like ulceration / intolerance to pain during the treatment. If patient wants alternate treatment during the study. If patient wants to discontinue the treatment.

Design outcomes

Primary

MeasureTime frame
The end point will be the evaluation of clinical response to both the mode of treatment at 36 weeks after treatment initiation Responses in between the study will be noticed recorded using Modified Vancouver Scar Scale(MVSS) Physicians Global Assessment (PGA) scale Patients overall satisfaction scoreTimepoint: 4 weeks

Secondary

MeasureTime frame
Safety profileTimepoint: 36 weeks

Countries

India

Contacts

Public ContactDrULAVANYA

Government Chengalpattu Medical college and hospital

dermcliniccmch@gmail.com9444767687

Outcome results

None listed

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