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A Study Comparing L PRF and Dermal Graft Techniques for Treating Mild to Moderate Gum Recession.

Comparative Evaluation of L-PRF and Acellular Dermal Matrix (ADM) in the Treatment of Miller s Class I and II Gingival Recession: A Randomized Controlled Clinical Trial. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110960
Enrollment
30
Registered
2026-05-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified

Interventions

Intervention1: L PRF: Patients treated using L PRF in millers class I and II gingival recession Control Intervention1: Acellular Dermal Matrix: Patients treated using ADM in millers class I and II

Sponsors

Dr.Ruchita Dilip Shahakar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age between 18 to 50 years 2 Presence of Class I or Class II gingival recession involving one or more teeth in the anterior or premolar esthetic zone 3 Systemically healthy individuals classified as ASA I 4 Full mouth plaque score and full mouth bleeding score less than or equal to twenty percent at the time of surgery 5 Patients with adequate oral hygiene compliance and willingness to follow postoperative instructions and recall visits 6 Vital teeth without periapical pathology at the defect site 7 Signed written informed consent for participation in the clinical study

Exclusion criteria

Exclusion criteria: 1 Class III or Class IV gingival recession defects 2 Evidence of active periodontal disease or generalized periodontitis 3 Uncontrolled systemic diseases such as diabetes mellitus cardiovascular disease or autoimmune disease 4 Smokers or tobacco users including those who quit within the last five years 5 Pregnant or lactating women 6 Use of antibiotics non steroidal anti inflammatory drugs anticoagulants corticosteroids or drugs affecting periodontal tissues in the last three months 7 History of periodontal surgery at the same site within the previous twelve months 8 Malpositioned teeth traumatic occlusion or orthodontic appliances interfering with soft tissue healing at the defect site 9 Bruxism parafunctional habits or high frenal pull at the treated site unless corrected 10 Allergy or contraindication to local anesthesia or study materials or inconsistent treatment protocol such as difference in prescribed medications between visits 11 Patient will be excluded if signs or symptoms aggravate the condition

Design outcomes

Primary

MeasureTime frame
Root coverage percentage Recession depth Keratinized mucosal width Timepoint: baseline 3 months 6 months

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Mangesh Phadnaik

Governmental Dental College and Hospital Nagpur

drmbphadnaik@gmail.com9422254404

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026