Two Surgical Approaches for Root Coverage of Teeth Presenting Gingival Recession and Non-carious Cervical Lesion

Sponsor
Universidade Estadual Paulista Júlio de Mesquita Filho (Other)
Overall Status
Completed
CT.gov ID
NCT03341598
Collaborator
(none)
60
1
2
17.8
3.4

Study Details

Study Description

Brief Summary

The aim of the present study is to compare the use of the xenogeneic graft (MC) plus coronary advanced flap (CAF) and the coronary advanced flap alone, both associated with the partial restoration of composite resin in the treatment of gingival recessions associated with non-carious cervical lesion.

Condition or Disease Intervention/Treatment Phase
  • Procedure: CAF
  • Procedure: R
  • Procedure: MC
N/A

Detailed Description

This is a prospective, parallel and controlled clinical trial. The population evaluated in the study was selected at Institute of Science and Technology (ICT), São José dos Campos, College of Dentistry.

Sixty patients presenting gingival recession will be divided in 2 groups:
  • Group 1 - Test: 30 gingival recessions associated with non-carious cervical lesions that will receive partial composite resin restoration and periodontal surgery for root coverage through a xenogenic collagen matrix graft (CAF + MC + R)

  • Group 2 - control: 30 gingival recessions associated with non-carious cervical lesions that will receive partial composite resin restoration and periodontal surgery for root coverage (CAF + R) without graft.

The surgeries, as well as all postoperative follow-up, were performed at the dental clinic of ICT. Two horizontal incisions were made at right angles to the adjacent interdental papillae, without interfering with the gingival margins of neighboring teeth. Two oblique vertical incisions were extended beyond the mucogingival junction, and a trapezoidal mucoperiosteal flap was raised up to the mucogingival junction. After this point, a split-thickness flap was extended apically, releasing the tension and favoring coronal positioning of the flap.The exposed root surface was gently scaled and planed until it became smooth in the connective tissue graft (CTG) group. For those allocated to CTG plus composite resin (CR) group, a sterile rubber dam was placed to isolate the operative field and the non-carious cervical lesion restoration was performed with a nanocomposite resin (Filtek Supreme - 3M - St. Paul, Minnesota, USA), following the manufacturer's instructions. Afterward, the both groups received a thin and small connective tissue graft that was sutured over the root/restoration surface. Then, the flap was coronally positioned and sutured to completely cover the graft.

Clinical parameters were assessed at baseline and 3 and 6 months post-operatively.

Statistical Analysis The null hypothesis considered in the study was the absence of difference in the clinical parameters between the different groups. For data analysis, the statistical program was used (SigmaPlot). The demographic and clinical data were compared between the groups using Student's t-test. The data were first analyzed for homogeneity using the Shapiro-Wilk test, which indicated non-normal distribution. . Those presenting Shapiro-Wilk p values < 0.05 were analyzed using a Friedman test (for intragroup comparisons) and Mann-Whitney tests (for intergroup comparisons). Patients' esthetics and discomfort measures using a visual analog scale (VAS) were analyzed by T-tests. The frequency of sites that were scored as very good or excellent in each group by qualitative cosmetic evaluation (QCE) analysis, the frequency of complete root coverage, bleeding on probing (BOP), and the presence or absence of plaque at the site were compared using χ2 tests. Intergroup root esthetic scale (RES) comparisons were performed with a T-test. A significance level of 0.05 was adopted.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of Different Surgical Approaches for Root Coverage of Teeth Presenting With Gingival Recession Associated With Non-carious Cervical Lesion Partially Restored With Composite Resin. Randomized Controlled Clinical Trial
Actual Study Start Date :
Feb 1, 2017
Actual Primary Completion Date :
May 4, 2018
Actual Study Completion Date :
Jul 27, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: CAF+R

First of all, a sterile rubber dam will be placed to isolate the operative field and the non-carious cervical lesion restoration was performed with a nanocomposite resin (Filtek Supreme - 3M- St. Paul, Minnesota, USA), following the manufacturer's instructions. CAF treatment will be performed by starting with two divergent releasing incisions lateral to the recessed area. A sulcular incision will be made to unite the releasing incisions and the flap will be raised beyond the mucogingival junction (MGJ) in split-full-split thickness. Sling sutures will be placed to stabilize the flap in a coronal position 2 mm above the cementoenamel junction (CEJ), followed by interrupted sutures to close the releasing incisions.

Procedure: CAF
Periodontal surgical technique to treat gingival recessions.
Other Names:
  • Periodontal plastic surgery
  • Procedure: R
    Restorative procedure to treat tooth structure loss.
    Other Names:
  • Composite resin restoration (Filtek Supreme - 3M)
  • Experimental: CAF+R+MC

    First of all, a sterile rubber dam will be placed to isolate the operative field and the non-carious cervical lesion restoration was performed with a nanocomposite resin (Filtek Supreme - 3M - St. Paul, Minnesota, USA), following the manufacturer's instructions. CAF treatment will be performed by starting with two divergent releasing incisions lateral to the recessed area. A sulcular incision will be made to unite the releasing incisions and the flap will be raised beyond the mucogingival junction (MGJ) in split-full-split thickness. Additionally, this group will receive the xenogenous collagen matrix graft (Geistlich) on the recessed area before the sutures. Then, the flap will be coronally positioned and sutured to completely cover the graft.

    Procedure: CAF
    Periodontal surgical technique to treat gingival recessions.
    Other Names:
  • Periodontal plastic surgery
  • Procedure: R
    Restorative procedure to treat tooth structure loss.
    Other Names:
  • Composite resin restoration (Filtek Supreme - 3M)
  • Procedure: MC
    Xenogenous graft placed in the surgical site.
    Other Names:
  • Xenogenous collagen matrix
  • Outcome Measures

    Primary Outcome Measures

    1. Recession reduction [1 year]

      Recession reduction from baseline measured in millimetres

    Secondary Outcome Measures

    1. Root coverage esthetic score [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • presenting Miller class I or II gingival recession in the maxillary canines or premolars associated with non-carious cervical lesion;

    • teeth included in the study should present pulp vitality;

    • patients presenting no signs of active periodontal disease and full-mouth plaque and bleeding score ≤ 20%;

    • patients older than 18 years old;

    • probing depth ˂ 3 mm in the included teeth;

    • patients who agreed to participate and signed an informed consent form

    Exclusion Criteria:
    • patients with systemic problems (cardiovascular, blood dyscrasias, immunodeficiency, and diabetes, among others) that will contraindicate the surgical procedure

    • patients taking medications known to interfere with the wound healing process or that contraindicate the surgical procedure

    • smokers or pregnant women

    • patients who underwent periodontal surgery in the area of interest;

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 São Paulo State University São José dos Campos São Paulo Brazil 12245000

    Sponsors and Collaborators

    • Universidade Estadual Paulista Júlio de Mesquita Filho

    Investigators

    • Principal Investigator: Mauro P Santamaria, PhD, ICT-UNESP

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Mauro Pedrine Santamaria, Assistant Professor, Universidade Estadual Paulista Júlio de Mesquita Filho
    ClinicalTrials.gov Identifier:
    NCT03341598
    Other Study ID Numbers:
    • UEPJMF 8
    First Posted:
    Nov 14, 2017
    Last Update Posted:
    Sep 2, 2020
    Last Verified:
    Aug 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 2, 2020