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NCT02939222

Impact of Buccal Bone Thickness on Pathological Peri-implant Bone Loss: A 3-year Prospective Cohort Study

Withdrawn NA Last updated 29 April 2020
What this trial tests

NA trial testing Implant placement in Periimplantitis. Withdrawn.

Timeline
1 October 2016
Primary endpoint
1 December 2021
1 December 2023

Quick facts

Lead sponsorCenter of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date1 October 2016
Primary completion1 December 2021
Estimated completion1 December 2023
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain — full company profile →

Who can join

Adults 18 to 80, any sex, with Periimplantitis or Oral Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Implant placement may trigger bone trauma, which might result in 3-dimensional bone changes. While the process of peri-implant disease is not well understood, implant position within the bony structure might play a role. However, there is no data available on this regard.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Implant placement

Trials testing the same drug.

Other recruiting trials for Periimplantitis

Currently open trials in the same condition.

Other Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02939222.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing