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To compare gum recession using Vista Technique by 2 grafts, either prf or amniotic membrane

Clinical Evaluation of Platelet Rich Fibrin versus Amniotic Membrane in treatment of Multiple Gingival Recession Defects using VISTA technique - A Randomised Clinical and 3-D Scan Study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101731
Enrollment
36
Registered
2026-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

None listed

Interventions

Intervention1: GROUP A = VISTA + Platelet Rich FIbrin: A single 8 10 mm vertical vestibular incision will be made, and a subperiosteal tunnel flap will be created extending 1 cm beyond recession site

Sponsors

Dr Charvi Raheja
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: 1. Multiple adjacent gingival recession Miller type I/II 2. The participants who are systemically healthy with good oral hygiene 3. Aged from 18 50 years

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA: 1. Systemic diseases interrupting the healing after surgical procedures 2. Patients who showed improper oral hygiene 3. Patients with Trauma from Occlusion 4. Smoking, and alcohol consumption 5. Patients with allergy to the Membrane used in the current study 6. Patients with cervical restoration in the facial surface of the involved tooth 7. Patients with high frenal pull 8. Patients received a periodontal surgery at the same location of designed treatment of gingival recession in the in the past 1 year.

Design outcomes

Primary

MeasureTime frame
Primary outcomes of the study: 1. GRD gingival recession depth, 2. KGW keratinized gingival width 3. RC% mean percent of root coverage 4. GTH - gingival thickness 5. To examine the volumetric changes in soft tissue aspects following root coverage using 3D ScanTimepoint: Baseline, 3 months, 6 months

Secondary

MeasureTime frame
Secondary outcomes of the study 1. PPD - probing pocket depth 2. CAL clinical attachment levelTimepoint: Baseline, 3 months, 6 months

Countries

India

Contacts

Public ContactDr Charvi Raheja

Dr. Harvansh Singh Judge Institute of Dental Sciences and Hospital, Chandigarh

charviraheja75@gmail.com06283727893

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026