Evaluating Implant Stability Using Three Devices Osstell®, Periotest® and AnyCheck®

Completed

• Conditions: Edentulous Alveolar Ridge

• Registration Number: NCT05340959
• Lead Sponsor: University of Baghdad

Brief Summary

A prospective observational study guided by the guidelines of Strengthening The Reporting Of Observational Study in Epidemiology (STROBE) in 2014, that will be conducted to evaluate implant stability using three devices; Osstell®, Peiotest® and AnyCheck® and comparing the results.

Detailed Description

In this study, 40 dental implants will be installed in osteotomy sites for patients with single or multiple missing tooth or teeth based on radiographic findings (CBCT).

The primary stability will be measured immediately after implant installation using three devices :

1. Osstell : based on resonance frequency analysis (RFA).

2. Periotest: based on damping effect.

3. AnyCheck: based on tapping motion. Secondary stability will be measured after 12 weeks using the same devices mentioned above.

Study Timeline

• Study Start: 2021-12-15
• Study First Submitted: 2022-03-27
• Study First Submitted QC: 2022-04-21
• Study First Posted: 2022-04-22
• Primary Completion: 2022-09-01
• Study Completion: 2022-12-01
• Status Verified: 2023-10
• Last Update Submitted: 2023-10-01
• Last Update Posted: 2023-10-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 16

Inclusion Criteria

1. Healthy patients over 18 years of either gender, having single or multiple missing teeth in the maxilla and/or mandible.
2. Patient with adequate vertical bone height and width for implant placement based on preoperative radiographic findings (CBCT).
3. Ability to tolerate conventional surgical and restorative procedures.
4. Patients who are willing to comply with the study and give their consent.

Exclusion Criteria

1. Active infection or inflammation in the implant zone.
2. Presence of any uncontrolled systemic diseases.
3. Patients with a history of radiotherapy to the head and neck.
4. Any patient requires advanced and complicated surgical techniques such as sinus lift and bone graft.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Implant stability measured by AnyCheck®.	Changes in implant stability from baseline value measured immediately after implant installation (primary stability) and after 12 weeks (secondary stability).	Implant stability will be measured by: AnyCheck® (tapping-motion) that is measured by Initial Stability Test (IST) Value.
Implant stability measured by Osstell®.	Changes in implant stability from baseline value measured immediately after implant installation (primary stability) and after 12 weeks (secondary stability).	Implant stability will be measured by: Osstell® (RFA) that is measured by Implant Stability Quotient (ISQ) Value.
Implant stability measured by Periotest®.	Changes in implant stability from baseline value measured immediately after implant installation (primary stability) and after 12 weeks (secondary stability).	Implant stability will be measured by: Periotest® (damping effect) that is measured by Periotest Value (PTV).
Correlation between values obtained by the devices	Changes in implant stability from baseline value measured immediately after implant installation (primary stability) and after 12 weeks (secondary stability).	Correlation between values obtained by: 1. Osstell® (RFA): measured by Implant Stability Quotient (ISQ) Value.; 2. Periotest® (damping effect): measured by Periotest Value (PTV).; 3. AnyCheck® (tapping-motion): measured by Initial Stability Test (IST) Value.

Trial Locations

Locations (1)

College of Dentistry, University of Baghdad; 🇮🇶 Baghdad, Medical City, Iraq