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Treatment of Gingival Recession-type Defects Using Different Restorative Materials

NCT02788266 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2016-06-02

No results posted yet for this study

Summary

Background: The aim of this study was to evaluate the treatment of multiple gingival recessions associated with non-carious cervical lesions (NCCL) using a modified coronally advanced flap in combination with a sub-epithelial connective tissue graft (SCTG) on restored root surfaces.

Methods: Twenty-three systemically healthy subjects, who were positive for the presence of three cervical lesions associated with gingival recessions in three different adjacent teeth, were enrolled in the study. The NCCL were each restored prior to surgery by using one of three different materials: composite resin (group 1), resin-modified glass ionomer cement (group 2) or giomer (group 3). The defects were treated with SCTG. Clinical measurements, including plaque index (PI), bleeding on probing (BOP), relative recession height (rRH), probing depth (PD), cervical lesion height (CLH), relative clinical attachment level (rCAL), keratinized tissue height (KTH), keratinized tissue thickness (KTT), percentage of root coverage (RC), and percentage of cervical lesion height coverage (CLHC) were recorded at baseline, 3 and 6 months, and 1 year postoperatively.

Conditions

  • Gingival Recession
  • Tooth Abrasion

Interventions

PROCEDURE

connective tissue graft+composite resin

treatment of gingival recession associated with cervical lesions with sub epithelial connective tissue graft plus composite resin

PROCEDURE

connective tissue graft+ glass ionomer

treatment of gingival recession associated with cervical lesions with sub epithelial connective tissue graft plus resin modified glass ionomer cement

PROCEDURE

connective tissue graft+giomer

treatment of gingival recession associated with cervical lesions with sub epithelial connective tissue graft plus giomer

Sponsors & Collaborators

  • Gazi University

    lead OTHER

Principal Investigators

  • gonen ozcan, Ph D · Prof.dr.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2016-01-31
Completion
2016-02-29

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02788266 on ClinicalTrials.gov