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Clinical Trials/NL-OMON39778
NL-OMON39778
Completed
Not Applicable

Clinical and microbiological evaluation of different implant surface decontaminating procedures in the surgical treatment of peri-implantitis; a randomized controlled study - Implant surface decontamination in peri-implantitis treatment

niversitair Medisch Centrum Groningen0 sites20 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
infection of the gingiva surrounding a dental implant
Sponsor
niversitair Medisch Centrum Groningen
Enrollment
20
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) The patient is \>\= 18 years of age;
  • 2\) The patient has at least one endosseous implant in the oral cavity with clinical and radiographical signs of periimplantitis. Peri\-implantitis is defined as a loss of marginal bone \>\= 2 mm as compared to a fixed reference point on the dental implant, in combination with bleeding and/or suppuration on probing and a peri\-implant probing depth \>\= 5 mm;
  • 3\) The implants have been exposed to the oral environment for at least two years;
  • 4\) The patient is capable of understanding and giving informed consent.

Exclusion Criteria

  • 1\) Medical and general contraindications for the surgical procedures;
  • 2\) A history of local radiotherapy to the head and neck region;
  • 3\) Pregnancy and lactation;
  • 4\) Insuline\-dependent diabetes;
  • 5\) Systemic use of antibiotics during the last 3 months;
  • 6\) Long\-term use of anti\-inflammatory drugs;
  • 7\) Incapability of performing basal oral hygiene measures as a result of physical or mental disorders;
  • 8\) Active, uncontrolled periodontal pathology of the natural dentition (PPD \> 5mm);
  • 9\) Implants placed in skin grafted areas;
  • 10\) Implants with bone loss due to other reasons than bacterial infection (e.g. loose screw, inadequate positioning of the implant);

Outcomes

Primary Outcomes

Not specified

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