Gingival Recession Clinical Trial
Official title:
Connective Tissue Graft vs Mucograft Collagen Matrix for Coverage of Multiple Gingival Recession Defects Randomized Controlled Clinical Trial Assessing Superiority in Health Related Quality of Life and Non-Inferiority in Root Coverage
This study deals with coverage of multiple denuded roots. The current standard treatment requires surgical correction and uses soft tissue taken from the roof of the mouth to enhance results. The hypothesis of this trial is that a synthetic collagen matrix (called Mucograft) can be used to replace soft tissue taken from the subject. If the collagen matrix will prove to be equally as effective as the patient own tissue, it will be possible to avoid a more extensive surgery and decrease pain and discomfort.
Objectives The main objective of this study is to assess if the Mucograft Collagen Matrix
reduces morbidity, shortens time to recovery and improves patient based outcomes with respect
to the use of autologous connective tissue graft harvested from the patient own palate when
used to obtain root coverage of multiple adjacent gingival recessions.
The secondary objective is to assess the non-inferiority - in terms of complete root
coverage, percentage of root coverage and professional evaluation of aesthetics - of the use
of Mucograft Collagen Matrix and autologous connective tissue harvested from the patient's
own palate.
Design and Outcomes This will be a parallel group, standard of care-controlled,
assessor-blind, randomized, multicenter, multinational, clinical trial.
The statistical design will be a superiority trial in terms of the primary outcomes (patient
based outcomes) and non-inferiority trial in terms of the professional outcomes measuring
root coverage and aesthetics.
Sample size has been estimated in 140 subjects per treatment arm using a pilot case series
analyzed with a multilevel statistical approach and a non inferiority margin of 0.25 mm in
recession coverage.
Randomization will be performed by computer generated random codes, using random permuted
blocks with a block size of 4 to avoid uneven splits and minimization for the key prognostic
factor cigarette smoking. Allocation will be concealed to the surgeons until completion of
preparation of the recipient bed by opaque envelopes. A central study registrar will perform
patient registration.
Study locations will include academic centers and a practice-based research network in Italy,
Switzerland, Germany, Belgium, France, Spain and Greece.
A single examiner, blind with respect to the treatment assignment, will perform all
measurements at each center. Trained personnel not involved with the surgical intervention
will: i) administer patient questionnaires, ii) provide instructions and collect patient
diaries. A single calibrated investigator with specific experience in using the specific
score will centrally perform assessment of esthetic scores on standardized digital images.
A biostatistician blind with respect to treatment assignment will perform the analysis.
Interventions and Duration The two intervention groups will consist of surgery with
connective tissue graft (standard of care control) and surgery with the application of
Mucograft Collagen Matrix (MCM, Test group). Experienced clinicians will deliver treatment
consisting of root coverage surgery using coronally advanced flaps, the most utilized
procedure for coverage of multiple recessions. Surgery will be standardized and the same
procedures/materials will be employed to ensure consistency.
Follow-up of individual patients will be 6 months (to be extended to 3 years if funding will
be available)
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