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Recruiting NCT06643507

Evaluation of the Modified VISTA Technique Using ALB-PRF vs CTG in the Treatment of Multiple Miller Class III Recessions

Phase II / Phase III Interventional Gingival Recession

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Connective tissue graft, ALB-PRF.
Who it may be relevant to
Registry conditions: Gingival Recession. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Clinical Evaluation of the Modified VISTA Technique (M-VISTA )Using Albumin-platelet Rich Fibrin (Alb-PRF) Versus Connective Tissue Graft (CTG)in the Treatment of Multiple Miler Class III RT2 Recessions A Randomized Clinical Trial

Overview

treatment of miller class III RT2 gingival recession using modified vista technique using connective tissue graft vs albumin PRF

Detailed description

treatment of gingival recession is an important element in the treatment of periodontitis this study covers clinical evaluation of using the modified VISTA technique with using Albumin-PRF VS connective tissue graft in the treatment of miller class III / RT2 for root coverage outcomes

Interventions

  • Other Connective tissue graft
    regenerative properties
  • Biological ALB-PRF
    regenerative properties

Primary outcome measures

  • mean root coverage [Time frame: 6 months]
Secondary outcome measures (6)
  • the percentage of mean root coverage [Time frame: 6 months]
  • the percentage of complete root coverage [Time frame: 6 months]
  • recession depth [Time frame: 6 months]
  • recession width [Time frame: 6 months]
  • keratinized tissue width [Time frame: 6 months]
  • clinical attachment level [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • 18 years old good oral hygiene

Exclusion criteria

  • smokers patients with poor oral hygiene

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of Dentistry Cairo University — Cairo

Identifiers

NCT: NCT06643507 · PER 3 -3 -1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗