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Study identifier: NCT07437417 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Novel Volume Stable Matrix for Gingival Recession Coverage at Teeth

Condition: Gingival Recession · Connective Tissue Defect  ·  Sponsor: University of Bern

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Periodontal health and preservation of the dentition without tooth loss are important quality of life components and should be safeguarded in order to provide optimal function and esthetics. Optimal treatment of gingiva recessions is likely to allow for more efficient use of healthcare resources and reduced costs long-term. It is evident that the prevalence in gingival recession is high and its consequences on the aging population constitute an important healthcare issue that requires further attention. The standard therapy of gingival recession encompasses a coronally advanced flap or coronally advanced tunnel flap and a connective tissue graft from the palate. Harvesting of the palatal graft involves a second surgical site and increased morbidity for the patients.This project aims to compare the connective tissue graft against a novel volume stable collagen matrix. Patients will be treated according to standard protocols of the Department of Periodontology. In the test group patient will undergo tissue thickening with a collagen matrix and the modified coronally advanced tunnel technique. The control group will undergo the standard protocol using a connective tissue graft from the palate along with the modified coronally advanced tunnel technique. No study specific risks do exist.

This description comes directly from the study's public registry record.

Talk to the study team

Anton Sculean, Prof  ·  +41 31 684 06 20  ·  anton.sculean@unibe.ch

Nikolaos Pandis  ·  +41 31 684 06 40  ·  nikolaos.pandis@unibe.ch

Always discuss trial participation with your own doctor first.

Locations (1)

Department of PeriodontologyBern, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT07437417