Clinical research on bone augmentation with Bio-Oss and B-TCP

Phase 3

• Conditions: patient planning dental implant surgery with loss of teeth and alveolar bone; dental implant

• Registration Number: JPRN-jRCTs022180044
• Lead Sponsor: KOYAMA SHIGETO

Brief Summary

We attempted to compare the clinical evaluation of Bio-Oss, a novel bone replacement material, when used non-approved for dental implants with beta-TCP in existing treatments, but discontinued the study due to noncompliance with the research plan.

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-03-26
• Study Completion: 2022-06-08
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 7

Inclusion Criteria

There are taken informed concent among dental implant patients at Tohoku University hospital

Exclusion Criteria

(1) the patients who refsed the consent for this study
(2) the patient judged to be unsuitable for study participation by doctor in charge

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. The amount of bone augmentation<br>2. CT value<br>3. ISQ at implant placement

Secondary Outcome Measures

Name	Time	Method
prognosis of implant