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Xenogeneic Collagen Matrix or Palatal Connective Tissue Graft With a Coronally Advanced Flap in Class III Recessions

Primary Purpose

Gingival Recession

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
experimental: collagen matrix
Active Comparator: autologous connective tissue graft
Sponsored by
University of the Basque Country (UPV/EHU)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gingival Recession focused on measuring Gingival recession, Collagen matrix, Connective tissue graft, Coronally advanced flap, Root coverage, keratinized tissue, Periodontal disease

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • The patient must be 18 years or older
  • Patient with one or more recession defects are Miller Class III in incisives, canines and premolars. In at least two quadrants
  • Patient shows sufficient plaque control (FMPS < 20%).
  • Treated periodontal conditions
  • The patient is able to fully understand the nature of the proposed surgery and is able to provide a signed informed consent.

Exclusion Criteria:

  • General contraindications for dental and/or surgical treatment are present.
  • The patient is taking medications or having treatments which have an effect on mucosal healing in general (e.g. steroids, large doses of anti-inflammatory drugs).
  • Untreated periodontal conditions
  • Patients not willing to participate

Sites / Locations

  • Department fo Stomatology II, Faculty of Medicine and Nursery, University of the Basque Country

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

autologous connective tissue graft

collagen matrix

Arm Description

Soft tissue harvesting from patient palate

Mucograft collagen matrix manufactured by Geistlich AG, Switzerland Device: Collagen matrix

Outcomes

Primary Outcome Measures

Percentage of root coverage
In each patient the mean of their gingival recessions at baseline (initial RECm)and at 6 (RECm 6months)and 12 months (RECm 12 months) will be calculated measuring at the mid buccal point of the involved teeth by the same blinded investigator using the same periodontal probe (PCP SE-11 Hu Friedly, Chicago, IL USA). With this measurements the percentage of root coverage will be calculated

Secondary Outcome Measures

Percentage of recessions with Complete root coverage
The number of recessions which after the treatment show complete root coverage (no recession) measured at the mid buccal point of the involved teeth at baseline and at 6 and 12 months .
Patient centred outcomes
At suture removal both procedures will be evaluated by the patient for discomfort, duration and difficulty on a visual analogue scale (VAS) . At 12 months the aesthetic outcome obtained with both treatment modalities will be appreciated by the patient on a VAS scale.
Gingival Thickness
The thickness in millimeters measured 3mm apically from the free gingival margin at the mid buccal aspect of the tooth
Keratinized Tissue width
Distance from the mucogingival junction to the gingival margin
Clinical Attachment Level
The gain of clinical attachment level in milimetres, compared with baseline
Recession width
Mesio-distal distance taken in the coronal area of the same, measured in millimeters.
Aesthetic results
The same blinded investigator will measured the aesthetic result by using the root coverage esthetic score system (RES)
Time of surgery
At surgery, the length of time of the full procedure will be evaluated (in minutes)

Full Information

First Posted
October 30, 2017
Last Updated
April 14, 2021
Sponsor
University of the Basque Country (UPV/EHU)
Collaborators
Geistlich Pharma AG
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1. Study Identification

Unique Protocol Identification Number
NCT03344315
Brief Title
Xenogeneic Collagen Matrix or Palatal Connective Tissue Graft With a Coronally Advanced Flap in Class III Recessions
Official Title
Xenogeneic Collagen Matrix or Palatal Connective Tissue Graft With a Coronally Advanced Flap for the Treatment of Miller Class III Gingival Recessions
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of the Basque Country (UPV/EHU)
Collaborators
Geistlich Pharma AG

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this multi-center study is to compare the effectiveness of Mucograft versus connective tissue graft in combination with coronal advanced flap for the treatment of Miller class III recessions The connective tissue graft in combination with coronal advanced flap is considered the gold standard for the treatment of gingival recession in terms of percentage of root coverage and complete root coverage. However connective tissue graft harvesting from the palatal mucosa is often associated with increased patient morbidity, prolonged surgical time and is limited supply. To overcome these inconvenients many efforts are made to develop new materials (healing modifiers, barrier membranes and grafts substitutes) Recently a new two-layer , xenogenic collagen matrix (Mucograft: Geistlich Pharma , Wolhusen Switzerland) has been proposed for regenerative therapy involving teeth and implants. The use of this porcine collagen matrix has obtained promising results for treatment of Miller class I and II recession defects (isolated and multiple recession defects) The mayority of root coverage studies in the literature treats Miller class I and II recession defects .Surgical treatment of class III recesión defects is more challenging due to loss of interproximal bone and soft tissues and complete root coverage may not be expected . But some recent studies demonstrate complete root coverage and high percentage of root coverage in class III recessions. Also a new classification system using the level of interproximal attachment level has been proposed to predict the final root coverage outcome. So ,the soft tissue substitutes should be used also in Miller class III recession, and because of that fact, the investigators are conducting this study, to evaluate the effectiveness of Mucograft in Miller class III recessions compared with connective tissue graft.
Detailed Description
Given data reported by the study of Aroca in 2013 ,using the percentage of root coverage as a primary response variable the sample size was estimated in 20 patients. In addition, taking into account possible drop-outs, the investigators would increase the number of patients by 20%, finally recruiting 24 patients per group. Randomization was performed by computer generated random codes Study locations will include two private centers in Spain. A single calibrated examiner, blind with respect to the treatment assignment, will perform all measurements at all center. A biostatistician blind with respect to treatment assignment will perform the analysis. Interventions and Duration The two intervention groups will consist of surgery with connective tissue graft (standard of care control) and surgery with the application of Mucograft Collagen Matrix (MCM, Test group). Experienced clinicians will deliver treatment consisting of root coverage surgery using coronally advanced flaps, the most utilized procedure for coverage of recessions. Surgery will be standardized and the same procedures/materials will be employed to ensure consistency. Follow-up of individual patients will be 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingival Recession
Keywords
Gingival recession, Collagen matrix, Connective tissue graft, Coronally advanced flap, Root coverage, keratinized tissue, Periodontal disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
split mouth
Masking
Outcomes Assessor
Masking Description
Observer: Another periodoncist outside the intervention, would be in charge of recording the clinical parameters. Analyst: The statistician does not know which treatment corresponds to each variable.
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
autologous connective tissue graft
Arm Type
Active Comparator
Arm Description
Soft tissue harvesting from patient palate
Arm Title
collagen matrix
Arm Type
Experimental
Arm Description
Mucograft collagen matrix manufactured by Geistlich AG, Switzerland Device: Collagen matrix
Intervention Type
Device
Intervention Name(s)
experimental: collagen matrix
Intervention Description
Mucograft collagen matrix combined with coronal advanced flap
Intervention Type
Other
Intervention Name(s)
Active Comparator: autologous connective tissue graft
Intervention Description
Soft tissue harvesting from patient palate with coronal advanced flap
Primary Outcome Measure Information:
Title
Percentage of root coverage
Description
In each patient the mean of their gingival recessions at baseline (initial RECm)and at 6 (RECm 6months)and 12 months (RECm 12 months) will be calculated measuring at the mid buccal point of the involved teeth by the same blinded investigator using the same periodontal probe (PCP SE-11 Hu Friedly, Chicago, IL USA). With this measurements the percentage of root coverage will be calculated
Time Frame
Change from baseline at following surgery sixth and twelfth month respectively
Secondary Outcome Measure Information:
Title
Percentage of recessions with Complete root coverage
Description
The number of recessions which after the treatment show complete root coverage (no recession) measured at the mid buccal point of the involved teeth at baseline and at 6 and 12 months .
Time Frame
Change from baseline at following surgery sixth and twelfth month respectively
Title
Patient centred outcomes
Description
At suture removal both procedures will be evaluated by the patient for discomfort, duration and difficulty on a visual analogue scale (VAS) . At 12 months the aesthetic outcome obtained with both treatment modalities will be appreciated by the patient on a VAS scale.
Time Frame
after surgery up to 7 days and 1 year
Title
Gingival Thickness
Description
The thickness in millimeters measured 3mm apically from the free gingival margin at the mid buccal aspect of the tooth
Time Frame
Change from baseline at following surgery and twelfth month respectively
Title
Keratinized Tissue width
Description
Distance from the mucogingival junction to the gingival margin
Time Frame
Change from baseline at following surgery sixth and twelfth month respectively
Title
Clinical Attachment Level
Description
The gain of clinical attachment level in milimetres, compared with baseline
Time Frame
Change from baseline at following surgery sixth and twelfth month respectively
Title
Recession width
Description
Mesio-distal distance taken in the coronal area of the same, measured in millimeters.
Time Frame
Change from baseline at following surgery sixth and twelfth month respectively
Title
Aesthetic results
Description
The same blinded investigator will measured the aesthetic result by using the root coverage esthetic score system (RES)
Time Frame
12 months
Title
Time of surgery
Description
At surgery, the length of time of the full procedure will be evaluated (in minutes)
Time Frame
After surgery up to 7 days

10. Eligibility

Sex
All
Gender Based
Yes
Gender Eligibility Description
18 years to 75 years
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The patient must be 18 years or older Patient with one or more recession defects are Miller Class III in incisives, canines and premolars. In at least two quadrants Patient shows sufficient plaque control (FMPS < 20%). Treated periodontal conditions The patient is able to fully understand the nature of the proposed surgery and is able to provide a signed informed consent. Exclusion Criteria: General contraindications for dental and/or surgical treatment are present. The patient is taking medications or having treatments which have an effect on mucosal healing in general (e.g. steroids, large doses of anti-inflammatory drugs). Untreated periodontal conditions Patients not willing to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luis Antonio Aguirre Zorzano
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Elena Ruiz de Gopegui Palacios
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Miren Vilor Fernandez
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ana Garcia de la Fuente
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ruth Estefania Fresco
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Xavier Marichalar Mendia
Organizational Affiliation
University of the Basque Country (UPV/EHU)
Official's Role
Study Chair
Facility Information:
Facility Name
Department fo Stomatology II, Faculty of Medicine and Nursery, University of the Basque Country
City
Leioa
State/Province
Biscay
ZIP/Postal Code
48940
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The data collected for the study will be identified by a code and only the researcher will be able to relate them. The personal data will be treated with absolute confidentiality in accordance with the Data Protection Law and will remain in the patient's clinical history. The coded data will be included in a UPV/EHU´s file with reference number 2080310015-INA0110, whose head is Ana María García de la Fuente, and will only be used for the purposes of this project.
Citations:
PubMed Identifier
23346965
Citation
Buti J, Baccini M, Nieri M, La Marca M, Pini-Prato GP. Bayesian network meta-analysis of root coverage procedures: ranking efficacy and identification of best treatment. J Clin Periodontol. 2013 Apr;40(4):372-86. doi: 10.1111/jcpe.12028. Epub 2013 Jan 24.
Results Reference
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Results Reference
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Wessel JR, Tatakis DN. Patient outcomes following subepithelial connective tissue graft and free gingival graft procedures. J Periodontol. 2008 Mar;79(3):425-30. doi: 10.1902/jop.2008.070325.
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Citation
Esteibar JR, Zorzano LA, Cundin EE, Blanco JD, Medina JR. Complete root coverage of Miller Class III recessions. Int J Periodontics Restorative Dent. 2011 Jul-Aug;31(4):e1-7.
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Xenogeneic Collagen Matrix or Palatal Connective Tissue Graft With a Coronally Advanced Flap in Class III Recessions

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