Clinical prospective Study for Patient Satisfaction with dental Implants
- Conditions
- Patient Satisfaction with dental implants
- Registration Number
- DRKS00022979
- Lead Sponsor
- Praxis Prof. Dr. Dr. Stoll und Partner
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 196
Participation in the implant recall system of Prof. Dr. Dr. Peter Stoll and Partner
- Consent to the use of personal data
- Voluntary completion of the questionnaire as well as written consent to participate in the study
- patients> 18 years
- Indication: Loss of a single tooth, free end gaps, gaps between teeth, fixed securing of dentures
- Patients with inadequate oral hygiene or patients who are unmotivated to perform adequate dental care at home
- Conditions or circumstances which, in the opinion of the examiner, would prevent the completion of the study participation or interfere with the analysis of the study results, e.g. non-compliance, false information or unreliability
- Physical or mental disabilities that would affect the ability to maintain proper oral hygiene
- Systemic diseases that interfere with dental implant therapy (e.g. uncontrolled diabetes)
- taking medication that interferes with dental implant therapy (e.g. intake of bisphosphonates)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Review of the patient's subjective perception after the insertion of dental implants, the quality of the treatment success is standardized and preconditioned.
- Secondary Outcome Measures
Name Time Method Recording of quality of life data with regard to implant loss, wearing time, the feeling of a foreign body, as well as the subjective satisfaction of patients with dental implants.