The Impact of Anti-Resorptive Agents on Dental Implant Success

This observational study aims to evaluate the relationship between the use of oral anti-resorptive agents and the success rate of dental implants in patients. Medical records from patients who received dental implants between January 2011 and December 2024 at National Taiwan University Hospital were reviewed. The study compares implant success rates between patients who had a history of oral anti-resorptive agents use and those who did not.

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Key information

Conditions

Dental Implant

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

National Taiwan University Hospital

Taipei, Zhongzheng Dist., 100, Taiwan

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age ≥ 20 years
with complete dental implant records
patients with or without a history of anti-resorptive agents

Exclusion criteria

patients lacking complete dental radiographic records
patients in whom the implant site or its relation to the lesion could not be clearly identified

Treatment and study plan

Primary outcomes

Dental implant success rate

Time frame: 12 months after implant placement

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Registry information

Official study title

The Impact of Anti-Resorptive Agents on Dental Implant Success: An Epidemiological, Meta-Analysis and Retrospective Cohort Study

Important dates

Study start: 2011
Primary completion: 2024
Study completion: 2025
First posted: Sep 2, 2025
Registry last updated: Sep 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed