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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03498911
Other study ID # HUM00140205
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2018
Est. completion date April 11, 2022

Study information

Verified date May 2022
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the influence of two different flap designs (envelope Coronally Advanced Flap (eCAF) and Modified Tunnel Technique (MTT)) with the addition of a connective tissue graft (CTG) in treating soft tissue dehiscences at implant sites


Description:

The primary aim is to compare the test and control groups in terms of: 1. mean mid-facial recession coverage (mRC) measured as a percentage 2. the keratinized tissue (KT) gain measured in mm 3. the keratinized tissue thickness (KTT) gain measured in mm. The secondary aims are to compare the two groups in terms of: 1. Esthetic score, using numeric values from 0 to 10 2. patient-reported esthetics, using numeric values from 1 to 5 3. patient-reported post-operative pain, based on Visual Analog Scale (VAS) scale, measured as numbers from 0 to 10.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date April 11, 2022
Est. primary completion date March 11, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years - Periodontally and systemically healthy - Full-mouth plaque score and full-mouth bleeding score = 20% (measured at four sites per tooth) - Correct implant 3-dimensional position or buccal position = 1 mm - Buccal soft tissue dehiscence = 4 mm - Only osseointegrated implants - The patient must be able to perform good oral hygiene Exclusion Criteria: - Contraindications for periodontal surgery - Patients pregnant or attempting to get pregnant - Malpositioned implant - Soft tissue dehiscence (STD) > 4 mm - Multiple adjacent implants with STD - Existing of peri-implantitis - Severe bone loss (=4mm) - Moderate-severe interproximal bone loss (implant fixture level to the alveolar bone > 3 mm) - Moderate-severe papilla height loss (Nordland and Tarnow implant papillae index >1) - Previous mucogingival surgery around the implant within the past six months or implant placement at the surgical site less than six months prior - Smoking more than 10 cigarettes a day

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Mucogingival surgery
The gingiva around the mucosal recession at implant site will be coronally positioned by releasing the underlying mucosa

Locations

Country Name City State
United States University of Michigan School of Dentistry Ann Arbor Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan Delta Dental Foundation

Country where clinical trial is conducted

United States, 

References & Publications (8)

Anderson LE, Inglehart MR, El-Kholy K, Eber R, Wang HL. Implant associated soft tissue defects in the anterior maxilla: a randomized control trial comparing subepithelial connective tissue graft and acellular dermal matrix allograft. Implant Dent. 2014 Au — View Citation

Bassetti RG, Stähli A, Bassetti MA, Sculean A. Soft tissue augmentation around osseointegrated and uncovered dental implants: a systematic review. Clin Oral Investig. 2017 Jan;21(1):53-70. doi: 10.1007/s00784-016-2007-9. Epub 2016 Nov 21. Review. — View Citation

Burkhardt R, Joss A, Lang NP. Soft tissue dehiscence coverage around endosseous implants: a prospective cohort study. Clin Oral Implants Res. 2008 May;19(5):451-7. doi: 10.1111/j.1600-0501.2007.01497.x. Epub 2008 Mar 26. — View Citation

Morelli T, Neiva R, Nevins ML, McGuire MK, Scheyer ET, Oh TJ, Braun TM, Nör JE, Bates D, Giannobile WV. Angiogenic biomarkers and healing of living cellular constructs. J Dent Res. 2011 Apr;90(4):456-62. doi: 10.1177/0022034510389334. Epub 2011 Jan 19. — View Citation

Roccuzzo M, Gaudioso L, Bunino M, Dalmasso P. Surgical treatment of buccal soft tissue recessions around single implants: 1-year results from a prospective pilot study. Clin Oral Implants Res. 2014 Jun;25(6):641-6. doi: 10.1111/clr.12149. Epub 2013 Apr 15 — View Citation

Schwarz F, Mihatovic I, Shirakata Y, Becker J, Bosshardt D, Sculean A. Treatment of soft tissue recessions at titanium implants using a resorbable collagen matrix: a pilot study. Clin Oral Implants Res. 2014 Jan;25(1):110-5. doi: 10.1111/clr.12042. Epub 2 — View Citation

Sculean A, Chappuis V, Cosgarea R. Coverage of mucosal recessions at dental implants. Periodontol 2000. 2017 Feb;73(1):134-140. doi: 10.1111/prd.12178. Review. — View Citation

Zucchelli G, Mazzotti C, Mounssif I, Mele M, Stefanini M, Montebugnoli L. A novel surgical-prosthetic approach for soft tissue dehiscence coverage around single implant. Clin Oral Implants Res. 2013 Sep;24(9):957-62. doi: 10.1111/clr.12003. Epub 2012 Aug — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary mean mid-facial recession coverage (mRC) mRC measured as a percentage up to 1 year
Secondary Esthetic score Esthetic score measured using numeric values from 0 to 10 6 months and 1 year
Secondary Patient-reported esthetics Patient-reported esthetics measured using numeric values from 1 to 5 6 months and 1 year
Secondary Patient-reported post-operative pain Patient-reported post-operative pain, based on VAS scale, measured as numbers from 0 to 10. 2 weeks
Secondary Keratinized tissue (KT) gain KT gain measured in mm 6 months and 1 year
Secondary Keratinized tissue thickness (KTT) KTT gain measured in mm 6 months and 1 year
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