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Effectiveness of Alveolar Bone Preservation in Alveoli With Infectious Process

Effectiveness of Autologous Bone and Bioactive Glass for Alveolar Preservation in Alveoli With Infectious Process

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06661863
Enrollment
28
Registered
2024-10-28
Start date
2024-11-15
Completion date
2029-12-15
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Loss

Keywords

Alveolar Resorption, Alveolar process, Bone Substitutes, Alveolar Bone Grafting

Brief summary

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

PROCEDUREalveolar ridge preservation with bioactive glass

Bioactive glass grafted into alveolar preservation.

PROCEDUREalveolar ridge preservation with autologous bone

Autologous bone graft in alveolar ridge preservation.

Sponsors

Universidad de Especialidades Espiritu Santo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

The participants will not know wich biomaterial will be grafted

Intervention model description

The study includes 28 patients who have a tooth extraction indicated in reference to g. avila-ortiz et al. 2020. They will be divided into 2 randomized groups, 14 sockets with an infectious process will be preserved with autologous bone and the remaining 14 with 58s bioactive glass

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
To evaluate bone formationThe 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.the dimensional bone changes of the preserved at each stage of healing will be analyzed by computer tomography

Countries

Ecuador

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026