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Observational study of scar outcomes in patients undergoing Dermaroller treatment with or without Platelet rich plasma (PRP)

Observational study of scar outcomes in patients undergoing microneedling with or without Platelet rich plasma (PRP) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/02/081177
Enrollment
20
Registered
2025-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: L919- Hypertrophic disorder of the skin,unspecified

Interventions

None listed

Sponsors

Tanvi Rao
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Scars secondary to trauma, burns or surgery Patient of any age if informed consent is obtained for the study by the patient or the guardian Patients who are not using other therapies for scar management

Exclusion criteria

Exclusion criteria: Patients who do not provide informed consent for the procedure Patients using other modalities of treatment for scar management Patients who have had permanent filler injections to scars Patients who are lost to follow up

Design outcomes

Secondary

MeasureTime frame
To evaluate POSAS score scars in patients undergoing microneedling and/or Platelet Rich Plasma (PRP)Timepoint: every 4 weeks—

Primary

MeasureTime frame
To evaluate outcomes of scars in patients undergoing microneedling and/or Platelet Rich Plasma (PRP)Timepoint: every 4 weeks—

Countries

India

Contacts

Public ContactTanvi Rao

Kasturba Medical college, Manipal

tanvi.rao@manipal.edu9483928989

Outcome results

None listed

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