Status:
UNKNOWN
SPiT-frequency; the Effect of Increased Frequency of Intervention on Post-surgical Peri-implant Inflammation
Lead Sponsor:
University of Oslo
Conditions:
Peri-Implantitis
Eligibility:
All Genders
20+ years
Phase:
NA
Brief Summary
This pilot study is an interventional clinical study on the supportive peri-implant treatment (SPiT) necessary to maintain/ improve the clinical conditions surrounding a dental implant following surgi...
Detailed Description
Patients with surgically treated peri-implantitis enrolled in a maintenance program at the Specialist clinic, Institute for Clinical Dentistry, Dental Faculty, University of Oslo, will receive SPiT by...
Eligibility Criteria
Inclusion
- Subject must be ≥ 20 years,
- Subjects must have received surgical treatment of peri-implantitis as defined by the World Workshop 2017 criteria (Berglundh et al., 2018).
- Subjects have to present inflammation (suppuration or BoP 3-2) at more than one implant of similar implant brand, with similar defect type (Schwarz et al., 2007), and defect severity.
- The implants must not be replacing adjacent teeth (minimum space for one tooth/implant between test and control.
Exclusion
- • Previous radiotherapy in the affected area, current use of chemotherapy, systemic long-term corticosteroid treatment.
- No pregnant or nursing subjects.
- \< class 2 according to the ASA (American Society of Anesthesiologists) physical status classification.
- Registered implant bone loss with exposed modified surface \< 2.0 mm.
- If examiners/operators agree the placement of the implant (angle, position, proximity to adjacent implant or tooth) or suprastructure was suboptimal and considered to play a major role in the development and sustain the peri-implant disease.
- Anatomical abnormalities
- clinical exclusion criteria specific to the disease/condition
- specific concomitant treatment with other devise, mouthrinse or systemic antibiotics
- participation in any other clinical study within the last month
- inability to comprehend and respond to the quality of life questionnaire
Key Trial Info
Start Date :
January 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 31 2023
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT04705012
Start Date
January 1 2023
End Date
August 31 2023
Last Update
November 3 2022
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