Last updated: April 29, 2024
Sponsor: Universitat Internacional de Catalunya
Overall Status: Active - Recruiting
Phase
N/A
Condition
Bone Density
Treatment
Customized allogenic bone block surgery
Clinical Study ID
NCT05937035
CIR-ECL-2022-02
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Signed informed consent
- Overall, healthy subjects (ASA1 and 2)
- Females and males of at least eighteen-years
- Requiring a posterior mandible rehabilitation with a minimum of 2 dental implants
- Able to follow instructions and attend a regular compliance
Exclusion
Exclusion Criteria:
- Acute local infection
- Untreated periodontal disease assessed by Socransky et al. parameters (≥ 2mm clinicalattachment loss in two consecutive visits within 1 year)
- Drug and/or alcoholic dependencies
- Medical conditions contraindicating implant surgery
- History of head and/or neck radiation
- Bisphosphonate therapy
Study Design
Total Participants: 10
Treatment Group(s): 1
Primary Treatment: Customized allogenic bone block surgery
Phase:
Study Start date:
May 25, 2024
Estimated Completion Date:
July 25, 2025
Study Description
Connect with a study center
Universitat Internacional de Catalunya
Sant Cugat Del Vallès, Barcelona 08195
SpainActive - Recruiting
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