Status:
TERMINATED
Novel Porous Bioceramic Material as a Bone Substitute
Lead Sponsor:
Orton Orthopaedic Hospital
Collaborating Sponsors:
Biomendex Oy
Oral Hammaslääkärit Oy, Qmedical Pikku Huopalahti
Conditions:
Alveolar Ridge Preservation
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The aim of this study is to demonstrate that new synthetic bone graft bioceramic composites (Adaptos®-Si and Adaptos®, Biomendex Oy) are able to support the preservation of the alveolar ridge and to p...
Detailed Description
The purpose of this study is to evaluate new synthetic Adaptos®-Si and Adaptos® in ridge preservation bone grafting after dental extraction. This is partly randomized, subject and outcome assessor-bli...
Eligibility Criteria
Inclusion
- Patient must have voluntarily signed the informed consent
- Females and males, 18 years to 80 years of age
- Patient needs single tooth extraction of 1st or 2nd premolar or molar tooth
- At least one adjacent teeth present
- At least 3 intact walls
- Subjects must be committed to the study and the required follow-up visits
Exclusion
- Planned radiation or radiation during previous year in the tooth extraction area.
- Smoking
- Osteoporosis
- Uncontrolled periodontitis
- Alcohol or drug abuse
- Pregnant or breastfeeding women
- Uncontrolled diabetes
- Local acute or chronic infection or presence of oral lesions or trauma
- Immunosuppressive disease, treatment, or medication
- Subject is part of the investigator team of this study or investigator's family member
- Subject is employee of one of the organizations involve in this study
Key Trial Info
Start Date :
June 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 27 2023
Estimated Enrollment :
76 Patients enrolled
Trial Details
Trial ID
NCT04719624
Start Date
June 1 2021
End Date
January 27 2023
Last Update
November 2 2023
Active Locations (1)
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1
Oral Hammaslääkärit Oyj, Qmedical Pikku Huopalahti
Helsinki, Finland, 00170