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Comparing the Effects of Platelet-Rich Fibrin (PRF) and Normal Saline Dressings on the Healing of Chronic Wounds

Effects of platelets rich fibrin & normal saline dressing in chronic wounds- A prospective randomized control trial. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079342
Enrollment
30
Registered
2025-01-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: T814- Infection following a procedure

Interventions

Intervention1: PRF dressings: PRF dressings done once a week for 6 weeks along with appropriate offloading method - surface area will be measured weekly Control Intervention1: Saline-gauze dressings:

Sponsors

Dr Dheerendra Kumar Mishra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age above 2 years and below 60 years (Male, Female & Transgender). 2.Non healing ulcers. 3.Serum platelet count more than 150000/dl. 4.Hb more than 9g/dl. 5.INR less than 1.5 6.Serum albumin more than 3.5g/dl. 7.Patients compliant to appropriate offloading procedure recommended by investigator.

Exclusion criteria

Exclusion criteria: 1.Wounds with signs of active local or systemic infection (Surrounding redness, local warmth, fever) 2.Wound size more than 50 cm2. 3.Diabetic patients with HbA1C more than 7%. 4.Radiological evidence of osteomyelitis of the underlying bone. 5.Immunocompromised states, uncontrolled systemic illnesses. 6.Patients on antiplatelet drugs. 7.Patients with mental illness or not able to give consent. 8.Patient refused to participate in study.

Design outcomes

Primary

MeasureTime frame
PEF Vs normal saline by comparing the weekly percentage reduction in the surface area of wounds after treatment in both groups.Timepoint: 4weeks and 3 months

Secondary

MeasureTime frame
effects of PRF during the treatment of chronic wounds.Timepoint: baseline, then every weekly till 6 weeks.

Countries

India

Contacts

Public ContactProf Dileep Kumar

King Georges Medical University Lucknow

dileepmsortho@yahoo.co.in7007636236

Outcome results

None listed

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