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A comparative study to assess efficacy of platelet rich plasma with silver sulphadiazine versus silver sulphadiazine dressing in partial thickness burns

A Randomised comparative study to assess efficacy of platelet rich plasma with silver sulphadiazine versus silver sulphadiazine dressing in partial thickness burns - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104410
Enrollment
40
Registered
2026-02-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: T311- Burns involving 10-19% of body surface

Interventions

Intervention1: AUTOLOGOUS Platelet rich plasma with silver sulphadiazine: Drop by drop, 7-8 CC of autologous PRP is gently poured onto the target area once in two days and allowed to dry for 15 minu

Sponsors

Bangalore medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Subjects with a deep partial-thickness burn injury covering 1- 20 % TBSA 2) Patient willing to give informed consent 3) Both sexes with an age of 2-60 years. 4)Subjects who were younger than the legal consenting age must have a legally authorized representative. 5) isolated burn area (not involving head and/or face)

Exclusion criteria

Exclusion criteria: 1)Subjects with inhalational injury or subjects being on a ventilator. 2)Treatment of the burn with an active agent before study entry. 3)Clinically infected burn 4)Diagnosed underlying disease(s) (e.g., HIV/AIDS, cancer, and severe anemia) Judged by the investigator to be a potential interference in the treatment. 5) Use of immunosuppressive agents, radiation, or chemotherapy within the past 30d. 6) Subjects with physical and/or mental conditions who are not expected to comply with the investigation. 7) Pregnancy 8)Patient with haematological or coagulation disorders 9)Patients with any chronic skin disease 10) Electric or chemical burns

Design outcomes

Primary

MeasureTime frame
Healing rate (epithelisation rate) Scar Score(Vancouver Scar Score) Pain Score Time until skin graft Ease of removal of the dressing Timepoint: dressing is done for 5 days , every alternate day , patients are studied and followed for 21 days - day 0, day 2, day 4, day 6, day 8, day 14 and day 21

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Anoosha Tresa Pius

bangalore medical college

rameshktr@yahoo.com9645630588

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026