Efficacy of a collagen matrix for soft tissue augmentation after implant placement compared to connective tissue grafts: A multicenter, noninferiority, randomized controlled trial

Author:

Hämmerle Christoph H. F.1ORCID,Jepsen Karin2,Sailer Irena3ORCID,Strasding Malin3ORCID,Zeltner Marco4,Cordaro Luca5ORCID,Mirisola di Torresanto Vincenzo5,Schwarz Frank6ORCID,Zuhr Otto7,Akakpo Dodji78,Bonnet Franck9,Sanz‐Martín Ignacio1011,Thoma Daniel S.1ORCID,Strauss Franz J.1ORCID,Sanz Mariano10

Affiliation:

1. Clinic of Reconstructive Dentistry University of Zurich Zurich Switzerland

2. Center for Dental and Oral Medicine, Department of Periodontology, Operative and Preventive Dentistry University Hospital Bonn Bonn Germany

3. Division of Fixed Prosthodontics and Biomaterials University of Geneva Geneva Switzerland

4. Private Practice Grimm Zahnaerzte Horgen Switzerland

5. Department of Periodontology and Prosthodontics, Eastman Dental Hospital University Policlinic Umberto I Rome Italy

6. Department of Oral Surgery and Implantlogy Carolinum Johan Wolfgang Goethe‐University Frankfurt Frankfurt Germany

7. Private Office Huerzeler/Zuhr Munich Germany

8. Private Practice DIE PRAXIS Berlin Germany

9. Private Practice Le Cannet France

10. ETEP Research Group (Etiology and Therapy of Periodontal and Peri‐implant Diseases) University Complutense Madrid Spain

11. Private Practice Lausanne Switzerland

Abstract

AbstractObjectivesTo test whether soft tissue volume augmentation using a collagen matrix (VCMX) leads to noninferior results in terms of gain of mucosal thickness at single implant sites, compared to connective tissue grafts (SCTG).MethodsThe study was designed as a multi‐center randomized controlled clinical trial. Subjects in need of soft tissue volume augmentation at single tooth implant sites were consecutively recruited at nine centers. The deficient mucosal thickness at the implant sites (one per patient) was augmented by applying either a VCMX or a SCTG. Patients were examined at 120 days (abutment connection = primary endpoint), 180 days (final restoration), and 360 days (1‐year after insertion of the final restoration). Outcome measures included: transmucosal probing of the mucosal thickness (crestal = primary outcome), profilometric measurements of the tissue volume, and patient‐reported outcome measures (PROMs).ResultsOut of the 88 patients, 79 attended the one‐year follow‐up. The median increase of the crestal mucosal thickness between pre‐augmentation and 120 days was 0.3 ± 2.1 mm in the VCMX group and 0.8 ± 1.6 mm in the SCTG group (p = .455). Non‐inferiority of the VCMX compared to the SCTG was not observed. The respective numbers at the buccal aspect amounted to 0.9 ± 2.0 mm (VCMX) and 1.1 ± 1.4 mm (SCTG; p = .431). PROMs including pain perception favored the VCMX group.ConclusionIt remains inconclusive whether soft tissue augmentation using a VCMX is noninferior to SCTG in terms of crestal mucosal thickening at single implant sites. However, the use of collagen matrices favors PROMs especially pain perception, while achieving similar buccal volume gains along with comparable clinical and aesthetic parameters to SCTG.

Funder

Geistlich Pharma

Publisher

Wiley

Subject

Oral Surgery

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