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Evaluation of efficacy of Platelet rich fibrin in healing of surgical removal of oral mucosal lesions

Efficacy of Platelet-rich fibrin as grafting material in wound healing following the surgical excision of oral mucosal lesions - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057224
Enrollment
90
Registered
2023-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: K132- Leukoplakia and other disturbancesof oral epithelium, including tongue

Interventions

Intervention1: platelet rich fibrin as a graft material: After surgical excision of oral mucosal lesions, Platelet-rich fibrin will be placed as a graft material. The study outcomes will be recorded o

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with oral mucosal lesions of size less than 5 cm in its greatest dimension. 2. Age group- 18-60 years

Exclusion criteria

Exclusion criteria: 1. With systemic diseases like diabetes mellitus, hypertension, thyroid disorders, immunocompromised state, etc. 2. H/O chemotherapy or radiotherapy 3. On long-term antibiotic, steroid or antiplatelets 4. Active local and/or systemic infection 5. Pregnant and lactating women and those taking oral contraceptives. 6. Hemoglobin level less than 10 gm/dL 7. Platelet count less than 100 ×103/µL 8. H/O allergy to local anesthetic agents like Xylocaine. 9. Chronic Alcoholic- >4 drinks/day or 14-15 drinks in a week. 10. Smoker- 100 cigarettes in his/her lifetime or currently smokes cigarettes.

Design outcomes

Primary

MeasureTime frame
1. Comparison of IPR healing scores between group 1, group 2 & group 3Timepoint: post-operative 4th day, 14th day, 6 weeks between the three groups.

Secondary

MeasureTime frame
1.Comparison of scores of VAS for severity of pain assessment 2.To record & compare the presence the granulation tissue formed 3.To record and compare the epithelization of wound 4.To record and compare the wound contracture 5.To record and compare any complicationsTimepoint: post-operative 4th day, 14th day, 6 weeks between the three groups

Countries

India

Contacts

Public ContactPooja Jain

Lady Hardinge Medical College

Surgeonrakesh10@yahoo.co.in8447642512

Outcome results

None listed

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