Prospective Observational Study of SynCone® Concept
Primary Purpose
Jaw, Edentulous
Status
Unknown status
Phase
Phase 1
Locations
Brazil
Study Type
Interventional
Intervention
Tapered abutment connection
Sponsored by
About this trial
This is an interventional treatment trial for Jaw, Edentulous
Eligibility Criteria
Inclusion Criteria:
- subject has total edentulous maxilla.
- subject whose dental extractions occurred at least 6 months before treatment.
Exclusion Criteria:
- pregnancy, lactation, smoking or ex-smokers, systemic conditions that could affect bone metabolism (e.g., immunologic disorders, diabetes), use of anti-inflammatory, biphosphonate, and immunosuppressive medications, subjects that required bone grafts before/during implant surgery.
Sites / Locations
- School of dentistry - Paulista University UNIPRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Syncone
Arm Description
Tapered abutment connection
Outcomes
Primary Outcome Measures
Modified Gingival Index
Index of mucosal condition (Mombelli et al.1987): 0 - No bleeding when a periodontal probe is passed along the mucosal margin adjacent to the implant, 1 - Isolated bleeding spots visible, 2 - Blood forms a confluent red line on mucosal margin, 3 - Heavy or profuse bleeding
Secondary Outcome Measures
Modified Plaque Index
Index of plaque accumulation (Mombelli et al.1987): 0 - No detection of plaque, Plaque only recognized by running a probe accross the smooth marginal surface of the implant, 2 - Plaque can be seen by the naked eye, 3 - Abundance of soft matter.
Oral Healthy Impact Profile-14 (OHIP-14)
A questionnaire will be administered to evaluate patient centered outcomes with regards to prosthesis. It has 14 questions in which the patient answers between never (0), rarely (1), sometimes (2), repeatedly (3) and always (4).
Microbiological assays
Peri-implant biofilm will be collected and Real Time PCR wil be performed to measure the absolute quantification of Aggregatibacter Actinomycetemcomitans, Porphyromonas gingivalis, and Tannerella forsythensis
Concentration of osteoimmuneinflammatory mediators
Levels of osteoimmuneinflammatory mediators will be determined in the peri-implant fluid (IL-4, IL-17, IL-1β, IL-10, IL-6, IL-8, IL-23 and TNF-α)
Crestal bone level
Periapical radiographs will be made to evaluate crestal bone level alteration.
Full Information
NCT ID
NCT03957265
First Posted
May 17, 2019
Last Updated
November 9, 2020
Sponsor
Marcio Zaffalon Casati
Collaborators
Dentsply Sirona Implants and Consumables
1. Study Identification
Unique Protocol Identification Number
NCT03957265
Brief Title
Prospective Observational Study of SynCone® Concept
Official Title
Prospective Observational Study of SynCone® Concept: Patient-related Outcomes, Clinical, Radiographic, Immunoinflammatory Mediators and Microbiological Analysis
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 3, 2021 (Anticipated)
Primary Completion Date
September 17, 2021 (Anticipated)
Study Completion Date
March 17, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Marcio Zaffalon Casati
Collaborators
Dentsply Sirona Implants and Consumables
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this prospective observational study will be to evaluate patient-related outcomes, clinical, microbiological and peri-implant immunoinflammatory mediators in completely edentulous patients rehabilitated with delayed loaded overdentures prostheses. The investigators hypothetize that this system could restore edentulous patients with healthier mucosal concerning clinical, microbiological and immunoinflammatory parameters, besides to promote improvement in patient satisfaction and quality of life.
Detailed Description
This prospective observational study will include fifteen edentulous patients rehabilitated with conventional dentures. Patients will receive four to six maxillary implants loaded three months after surgery. Clinical, microbiological and immunoinflammatory parameters will be evaluated at baseline, three, and six months following overdenture prosthesis. Patient-centered/reported outcomes concerning general satisfaction with the prostheses as well as comfort, ability to speak, stability, esthetics, ease of cleaning and occlusion, will be evaluated at baseline (conventional denture evaluation) and after 6 months (overdenture evaluation).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Jaw, Edentulous
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Syncone
Arm Type
Experimental
Arm Description
Tapered abutment connection
Intervention Type
Procedure
Intervention Name(s)
Tapered abutment connection
Intervention Description
Rehabilitation of completely edentulous patients with overdentures prostheses.
Primary Outcome Measure Information:
Title
Modified Gingival Index
Description
Index of mucosal condition (Mombelli et al.1987): 0 - No bleeding when a periodontal probe is passed along the mucosal margin adjacent to the implant, 1 - Isolated bleeding spots visible, 2 - Blood forms a confluent red line on mucosal margin, 3 - Heavy or profuse bleeding
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Modified Plaque Index
Description
Index of plaque accumulation (Mombelli et al.1987): 0 - No detection of plaque, Plaque only recognized by running a probe accross the smooth marginal surface of the implant, 2 - Plaque can be seen by the naked eye, 3 - Abundance of soft matter.
Time Frame
6 months
Title
Oral Healthy Impact Profile-14 (OHIP-14)
Description
A questionnaire will be administered to evaluate patient centered outcomes with regards to prosthesis. It has 14 questions in which the patient answers between never (0), rarely (1), sometimes (2), repeatedly (3) and always (4).
Time Frame
6 months
Title
Microbiological assays
Description
Peri-implant biofilm will be collected and Real Time PCR wil be performed to measure the absolute quantification of Aggregatibacter Actinomycetemcomitans, Porphyromonas gingivalis, and Tannerella forsythensis
Time Frame
6 months
Title
Concentration of osteoimmuneinflammatory mediators
Description
Levels of osteoimmuneinflammatory mediators will be determined in the peri-implant fluid (IL-4, IL-17, IL-1β, IL-10, IL-6, IL-8, IL-23 and TNF-α)
Time Frame
6 months
Title
Crestal bone level
Description
Periapical radiographs will be made to evaluate crestal bone level alteration.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
subject has total edentulous maxilla.
subject whose dental extractions occurred at least 6 months before treatment.
Exclusion Criteria:
pregnancy, lactation, smoking or ex-smokers, systemic conditions that could affect bone metabolism (e.g., immunologic disorders, diabetes), use of anti-inflammatory, biphosphonate, and immunosuppressive medications, subjects that required bone grafts before/during implant surgery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
marcio casati
Phone
55 11 981625664
Email
mzcasati@gmail.com
Facility Information:
Facility Name
School of dentistry - Paulista University UNIP
City
São Paulo
State/Province
SP
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fernanda V Ribeiro, Professor
Phone
55 11 71388342
Email
fernanda@ribbeiro.com
12. IPD Sharing Statement
Plan to Share IPD
No
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Prospective Observational Study of SynCone® Concept
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