Clinical evaluation research of GC Implant Aadva

Not Applicable

• Conditions: single or continuous two teeth loss

• Registration Number: JPRN-UMIN000013718
• Lead Sponsor: Kyushu University Faculty of Dental Science Implant and Rehabilitative Dentistry

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2014-04-15
• Study Completion: 2019-03-11
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Not provided

Exclusion Criteria

1.Subjects with a systemic disease that may affect the implant treatment, diabetes for example 2.Subjects with any of the diseases that is contraindicated or relatively contraindicated in oral surgical treatment disorders 3.Subjects with tooth root at planned implantation 4. Subjects with bone graft to the extraction socket 5. Subjects with an untreated tooth that needs endodontic care in an adjacent part of the implant placement site 6. Subjects with a 4-mm or deeper periodontal pocket in an adjacent tooth of the implant placement site 7. Subjects with un-control of periodontal disease 8. Subjects with severe habits of bruxism or clenching 9. Subjects with extremely short intermaxillary distance or notable trismus due to temporomandibular joint dysfunction 10. Subjects with extreme occlusion failure 11. Subjects who smoke more than 10 cigarettes a day or subjects who cannot stop smoking for 2 weeks before and after the implant placement surgery 12. Subjects who plan to participate in other clinical trial, or investigation 30 days prior to or during this study 13. Subjects who are pregnant or nursing or subjects who plan to be pregnant during this study 14. Subjects who cannot understand this study or subjects that the investigator deems ineligible to participate in this study 15. Subjects who can not be mutual understanding or mental illness 16. Uncooperative subjects to treatment 17. Subjects who need sinus lift 18. Subjects with a history of failure of implant placement in the site where an implant is planned to be placed in this study 19. Subjects within 12 weeks of tooth extraction

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
amount of marginal bone loss after implant loading

Secondary Outcome Measures

Name	Time	Method
Evaluation of implant success/survival Shaking of implant and pain Rubor of peri implant tissue Pus discharge Exposure of implant Oral hygiene