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Use of minimally invasive technique for gingival recession coverage.

Evaluation of Leukocyte - Platelet Rich Fibrin (L-PRF) and Titanium prepared Platelet Rich Fibrin (T-PRF) as adjuncts to Vestibular Incision Subperiosteal Tunnel Access (VISTA) technique under magnification in the treatment of multiple gingival recession defects A Randomized Controlled Trial. - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110084
Enrollment
26
Registered
2026-05-06
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

None listed

Interventions

Intervention1: VISTA : VISTA technique under magnification will be used to cover multiple gingival recession defects. Control Intervention1: GROUP II: T-PRF + VISTA Under magnification.: patients wil

Sponsors

NONE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 age between 18-55 years 2 systemically healthy individual 3 good oral hygiene 4 non-smoker 5 willing to participate 6 miller class I OR IIrecession defect 7 adequate vestibular depth 8 no previous mucogingival surgery at the selected site.

Exclusion criteria

Exclusion criteria: 1 systemic diseasees interrupting the healing after surgical procedure 2 patients with TFO 3 Smoking and alcohol comsumption 4 patient with high frenal pull 5 miller class III OR IV recession 6 cervical caries or non carious lesion requiring restoration 7 patients with poor oral hygiene 8 active periodontal disease

Design outcomes

Primary

MeasureTime frame
Gingival Recession Coverage (using parameters Recession depth, Percentage root coverage and Clinical attachment level ) will be assessed in both the groups.Timepoint: follow up will be done 3 months and 6 months post-operatively.

Secondary

MeasureTime frame
1gingival thickness 2 width of keratinized gingiva 3 probing depth 4 wound healing index 5 esthetic outcome assessment 6 visual analogue scale .Timepoint: baseline , 3 months & 6 months post -operatively

Countries

India

Contacts

Public ContactJESSICA DANG

Dr. Harvansh Singh Judge Institute of Dental Sciences and Hospital

nandini.chhabra@yahoo.co.in9876166768

Outcome results

None listed

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