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Periapical Lesions and Immediate Implants

A

Akdeniz University

Status

Completed

Conditions

Periapical Granuloma
Osseointegration Failure of Dental Implant
Dental Implant Failure Nos

Study type

Observational

Funder types

Other

Identifiers

NCT06521203
20022019/188

Details and patient eligibility

About

The aim of this case-control study is to evaluate the success and survival rates of dental implants immediately placed into extraction sites in the presence of periapical pathology.

The main questions it aims to answer are:

What were the survival and success rates of implants immediately placed into extraction sockets of teeth with chronic periodical lesions.

A retrospective analysis was performed based on the evaluation of certain clinical and radiographic parameters 12 months after prosthetic function of these implants.

Full description

In 25 patients (13 men, 12 women), certain clinical and radiological parameters were retrospectively evaluated with particular interest in survival and success rates of the implants (total of 30 implants, 21 in the maxilla, 9 in the mandible) placed immediately to extraction sites of teeth with chronic periapical lesions. These parameters included mobility and the presence or absence of chronic pain, probing depth, gingival index, radiographic measurements of crestal bone loss on mesial and distal aspects of the implants.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • To have 1 or more teeth with a chronic periapical lesion that requiring extraction.
  • The chronic periapical lesion should be determined as an asymptomatic periapical radiolucency with a diameter ranging between 4 and 8 mm.
  • The patients undergoing tooth extraction must have been treated with an immediate implant placement procedure.
  • At the time of extraction and implant placement, the neighboring teeth must have had healthy periodontal and periapical status.

Exclusion criteria

  • Age younger than 18 years
  • Any systemic disease or medication that might compromise osseointegration, bone or soft tissue healing
  • Smoking
  • Purulent exudate during the extraction
  • Severe deficiency of soft and/or hard tissue in implant region
  • Pregnancy
  • Lactation
  • History of chemotherapy or radiotherapy
  • Severe parafunctional habits

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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