Evaluation of initial crestal bone loss dependent on insertion torque with Progressive-Line implants: a retrospective data analysis.
- Conditions
- K08.1Loss of teeth due to accident, extraction or local periodontal disease
- Registration Number
- DRKS00029995
- Lead Sponsor
- Implantatzentrum Dr. Ruppin & Kollegen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 63
Inclusion Criteria
1. men and women aged 18 years and plus.
2. presence of one or more CAMLOG PROGRESSIVE-LINE implants as single tooth restoration(s) in the maxilla and/or mandible with implant surgery starting from 01.01.2021.
3. treatment plan with closed/submerged healing of the implants of at least 3 months.
4. patients who have appeared for the re-entry visit of the implant(s).
Exclusion Criteria
5. contraindications to oral surgery.
6. surgical complications that could affect healing, especially dehiscence, wound healing disorders and prosthetic pressure points.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary implant stability at insertion: insertion torque in Ncm, ISQ (RFA, Osstell Beacon measuring device), X-ray images.
- Secondary Outcome Measures
Name Time Method - Evaluation / measurement of the X-ray images according to crestal bone level (mesial and distal of implant neck) at the time of surgery and re-entry.<br>- Secondary implant stability: ISQ (RFA, Osstell Beacon)<br>- Bone class of the implant site<br>- Complications