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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03523845
Other study ID # LPI1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1996
Est. completion date December 2016

Study information

Verified date May 2018
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

A case-control study was performed was performed following the STROBE statement from 1996 to 2016 including patients who were diagnosed with early apical peri-implantitis. Data were collected at the time of implant placement, and once the patients developed signs and symptoms consistent with early apical peri-implantitis, to determine the frequency and etiology of this pathology.


Description:

A case-control study was performed following the STROBE statement (17) at the Oral Surgery Department, Faculty of Medicine and Dentistry (University of Valencia, Spain) from 1996 to 2016, in which patients with early peri-implantitis diagnosed were included (Figure 1). All patients were informed about the study design and procedures. Prior to participating, they were requested to sign an informed consent document. The study design was approved by the Ethical Committee of the University of Valencia (H1478255958653).

Two groups were established: Test group (patients diagnosed with early apical peri-implantitis diagnosed) and Control group (patients whose implants had not developed any inflammatory/infectious process and were osseointegrated).


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- The following inclusion criteria were applied: patients =18 years old and controlled medical conditions who received treatment with implants. Additionally, for the test group, inclusion criteria were: symptoms and signs suggesting early apical peri-implantitis after implant placement; absence of implant mobility; dull percussion of nonsurmerged implants; presence or absence of radiolucency apically.

Exclusion Criteria:

- for the both groups: implants placed with guided bone regeneration or inadequate follow-up for failing to maintenance visits.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational intervention to diagnose an early apical peri-implantitis
diagnose an early apical peri-implantitis

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

References & Publications (4)

Lefever D, Van Assche N, Temmerman A, Teughels W, Quirynen M. Aetiology, microbiology and therapy of periapical lesions around oral implants: a retrospective analysis. J Clin Periodontol. 2013 Mar;40(3):296-302. doi: 10.1111/jcpe.12045. Epub 2012 Dec 27. — View Citation

Peñarrocha-Diago M, Maestre-Ferrín L, Cervera-Ballester J, Peñarrocha-Oltra D. Implant periapical lesion: diagnosis and treatment. Med Oral Patol Oral Cir Bucal. 2012 Nov 1;17(6):e1023-7. — View Citation

Quirynen M, Gijbels F, Jacobs R. An infected jawbone site compromising successful osseointegration. Periodontol 2000. 2003;33:129-44. Review. — View Citation

Zhao D, Wu Y, Xu C, Zhang F. Immediate dental implant placement into infected vs. non-infected sockets: a meta-analysis. Clin Oral Implants Res. 2016 Oct;27(10):1290-1296. doi: 10.1111/clr.12739. Epub 2015 Dec 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary type of surgery immediate/delayed placement Intraoperative
Primary tooth-implant distance mesial and distal tooth-implant distance measured at the apex Intraoperative
Primary Tooth status apical lesion or endodontic treatment in the tooth being replaced or adjacent tooth endodontically treated Intraoperative