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Follow-Up After Surgical Treatment of Peri-implantitis

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ClinicalTrials.gov Identifier: NCT02860208
Recruitment Status : Completed
First Posted : August 9, 2016
Last Update Posted : December 20, 2016
Sponsor:
Information provided by (Responsible Party):
Göteborg University

Brief Summary:
The objective of this prospective clinical study was to evaluate the 3-year outcomes of anti-infective surgical treatment of peri-implantitis when a regular supportive peri-implant therapy (SPIT) programme was followed.

Condition or disease Intervention/treatment
Peri-Implantitis Procedure: 3 years follow-up

Detailed Description:

The patients enrolled in this prospective study all received surgical treatment for peri-implantitis at one of 2 treatment centres (specialist periodontal practice, Molndal and Gothenburg, Public Dental Health Services, Region Vastra Gotaland, Sweden) and were enrolled between October 2010 and December 2013.). All were treated by experienced periodontists.

Details of the peri-implantitis treatment protocol have been described in a previous publication reporting on the 12-month clinical and radiographic treatment outcomes, registered at ClinicalTrials.gov (NCT01857804) and approved by the Regional Ethical Committee, Gothenburg, Sweden (Dnr. 654-10).

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Study Type : Observational
Actual Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Follow-Up After Surgical Treatment of Peri-implantitis
Study Start Date : December 2013
Actual Primary Completion Date : December 2016
Actual Study Completion Date : December 2016

Group/Cohort Intervention/treatment
3 years follow-up
all patients who received surgical treatment for peri-implantitis during a Randomized and Controlled Trial registered in ClinicalTrials.gov NCT NCT01857804
Procedure: 3 years follow-up
Examination 3 years after surgical treatment of peri-implantitis




Primary Outcome Measures :
  1. Change from baseline in treatment success at 3 years post-op [ Time Frame: baseline (1 year post-op) and 3 years post-op ]
    treatment success is defined by pocket closure, no bleeding on probing, bone loss ≤0.5 mm between baseline and 3 years



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
all patients who received surgical treatment for peri-implantitis during the RCT registered in ClinicalTrials.gov NCT NCT01857804
Criteria

Inclusion Criteria:

  • all patients who received surgical treatment for peri-implantitis for 3 years ago

Exclusion Criteria:

-


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02860208


Sponsors and Collaborators
Göteborg University
Investigators
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Study Chair: Tord Berglundh, Professor Department of Periodontology, Institute of Odontology, The sahlgrenska academy, University of Gothenburg
Publications:

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Responsible Party: Göteborg University
ClinicalTrials.gov Identifier: NCT02860208    
Other Study ID Numbers: olivier2
First Posted: August 9, 2016    Key Record Dates
Last Update Posted: December 20, 2016
Last Verified: December 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by Göteborg University:
Peri-Implantitis
Surgical therapy
Follow-up
Supportive peri-implant therapy
Additional relevant MeSH terms:
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Peri-Implantitis
Periodontal Diseases
Mouth Diseases
Stomatognathic Diseases