Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07200258

Changes in Soft Tissue Thickness Following Multiple Coronally Advanced Tunnel (MCAT) vs Vestibular Incision Subperiosteal Tunnel Access (VISTA): A Randomized Clinical Trial With 3D Volumetric Analysis

Led by Universidad Complutense de Madrid · Updated on 2026-02-13

44

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are comparing two surgical methods for treating multiple adjacent gingival recessions, types RT1 and RT2: the Modified Coronally Advanced Tunnel (MCAT) and the Vestibular Incision Subperiosteal Tunnel Access (VISTA). Both methods use connective tissue grafts (CTG) to cover exposed tooth roots. This randomized clinical trial aims to assess changes in soft tissue thickness using three-dimensional digital volumetric analysis at six and 12 months. Secondary outcomes include root coverage, esthetic results, gum health, sensitivity, patient satisfaction, and wound healing quality. Participants will be randomly assigned to either the VISTA or MCAT group. The VISTA technique involves remote vestibular incisions and creating a subperiosteal tunnel for graft placement, stabilized with sutures anchored coronally. The MCAT technique uses sulcular incisions without releasing incisions, raising a full-thickness tunnel beyond the mucogingival junction where the connective tissue graft is inserted and secured with horizontal mattress sutures. Both procedures are performed under local anesthesia by periodontal specialists in training. Follow-up evaluations will occur up to 12 months post-surgery. During the study, participants will attend multiple visits for assessments including measurements of soft tissue thickness, root coverage, probing depth, gingival thickness, and oral health impact. Digital tools will be used to analyze tissue changes, and evaluations of hypersensitivity, esthetics, wound healing, and patient concerns will be recorded at various time points from baseline to 12 months. The total participation duration spans from surgery through a year of follow-up to monitor healing and treatment outcomes.

CONDITIONS

Brief Title

Changes in Soft Tissue Thickness Following Multiple Coronally Advanced Tunnel (MCAT) vs Vestibular Incision Subperiosteal Tunnel Access (VISTA)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Periodontally and systemically healthy adults aged 18 years or older
  • At least two adjacent sites with gingival recessions classified as type 1 (RT1) or type 2 (RT2)
  • Presence of at least 2 mm depth on one or more recessions
  • Smokers who smoke 10 or fewer cigarettes per day
  • Full-mouth plaque and bleeding scores of 20% or less
  • Ability to maintain good oral hygiene
Not Eligible

You will not qualify if you...

  • Compromised general health
  • Pregnancy or attempting to get pregnant
  • Untreated periodontal diseases
  • Severe tooth malposition
  • Root caries or inadequate prosthetic restorations
  • Previous periodontal plastic surgery at the experimental sites
  • Smoking more than 10 cigarettes per day

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Day of surgery

Participants undergo surgical treatment using either the Vestibular Incision Subperiosteal Tunnel Access (VISTA) technique or the Modified Coronally Advanced Tunnel (MCAT) technique to treat gingival recessions.

1 surgery visit (in-person)

Post-operative Follow-up

Duration - Up to 12 months

Participants are monitored regularly after surgery to assess healing, soft tissue changes, and treatment outcomes.

Visits at Day 7, Week 2, Week 4, and at 3, 6, and 12 months post-surgery (in-person)

Trial Site Locations

Total: 1 location

1

University Complutense of Madrid

Madrid, Spain

Actively Recruiting

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Research Team

A

Ana Carrillo de Albornoz Sainz

T

Tommaso Conforti

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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