Effectiveness of Alveolar Bone Preservation in Alveoli With Infectious Process
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: alveolar ridge preservation with bioactive glass, alveolar ridge preservation with autologous bone.
- Who it may be relevant to
- Registry conditions: Alveolar Bone Loss. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Ecuador
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effectiveness of Autologous Bone and Bioactive Glass for Alveolar Preservation in Alveoli With Infectious Process
Overview
Alveolar ridge preservation (ARP) is a surgical technique that aims to minimize the degree of dimensional changes following extraction. In the healing period after extraction, the alveolar bone (AB) undergoes morphological changes during the remodeling process. The changes become evident immediately after tooth extraction, with greater resorption changes observed during the first two months, and these dimensional changes can be observed 1 year after surgery.
Interventions
- Procedure alveolar ridge preservation with bioactive glass
Bioactive glass grafted into alveolar preservation. - Procedure alveolar ridge preservation with autologous bone
Autologous bone graft in alveolar ridge preservation.
Primary outcome measures
- To evaluate bone formation [Time frame: The evaluation will occur from enrollment through the end of treatment at 12 months. Assessments will be conducted preoperatively, 7 days post-surgery, as well as at 3, 6, and 12 months following the surgery.]
Eligibility criteria
Inclusion criteria
- Patients over 18 years of age
- Patients with indicated tooth extractions
- Patients who have accepted the conditions of the study
Exclusion criteria
- Pregnant patients, breastfeeding or using oral contraceptives
- Smoking patients
- Patients with uncontrolled systemic diseases
- History of autoimmune disease
- Previous traumatic extraction
- Patients taking bisphosphonates or anticoagulants
- Patients who are or have undergone chemotherapy and radiotherapy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Ecuador · 1 center
- Universidadees — Samborondón
Identifiers
NCT: NCT06661863 · 2024-ODONT-002C