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Evaluation of the Osteoinductivity of Atorvastatin Combined With β-TCP

Evaluation of the Osteoinductivity of Atorvastatin Combined With β-TCP in the Treatment of Bone Defects After Radicular Jaw Cyst Enucleation Using CBCT-based Volumetric Analysis

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06382974
Enrollment
10
Registered
2024-04-25
Start date
2024-12-31
Completion date
2026-03-31
Last updated
2024-08-13

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

Conditions

Bone Loss, Infection

Keywords

bone regeneration, bone graft, volumetric analysis

Brief summary

This case series study aims to evaluate the local effects of Atorvastatin (which belongs to the family of lipid-lowering drugs, known as statins) combined with β-TCP (which is a synthetic osteoconductive bone graft), on the volume of the residual bone defects and on hastening the bone regeneration after radicular jaw cyst enucleation using CBCT-based volumetric analysis to calculate the shrinkage rate of these defects.

Detailed description

Statement of the problem: According to the literature, the residual bone defects after medium-large-sized jaw cyst enucleation pose the risk for infection, insufficient healing, and pathological fracture. the gold standard of bone grafting materials remains the autologous bone graft, yet it is accompanied by risks including second surgery, the morbidity of the donor site, excessive bleeding, etc. Therefore, there is a constant search for alternative bone grafting materials, this is where the addition of atorvastatin to an osteoconductive synthetic bone grafting material (β-TCP) comes in. β-TCP takes anywhere from 6 to 18 months for complete resorption and replacement by bone, according to the literature. The addition of an osteoinductive material to an osteoconductive grafting material like β-TCP holds two premises; increasing the resorption of the β-TCP particles at the expense of bone deposition, and therefore leads to hastening the bone generation of the residual bone defects. Rationale: Studies have shown that the local application of lipid-lowering drugs, statins, induces bone growth by stimulating BMP-2. therefore, the addition of these pharmacological agents to osteoconductive bone graft materials, which lack osteogenic properties, could be a promising approach for bone regeneration. However, there is still no consensus in the literature on the optimal therapeutic dose and mode of application for statins. Furthermore, limited studies are available in the literature regarding the use of statins especially Atorvastatin as a biological modifier in filling bone defects after cyst enucleation. Therefore, the purpose of this study is to validate and evaluate the osteoinductivity of statins+ β-TCP combination using the Gouda et al., methodology used in maxillary sinus lifting using simvastatin but instead using atorvastatin in filling the residual defects of medium-large odontogenic radicular cysts (1.5 - 4 cm), which shows the suppressive influence on bone formation, as well as a greater risk for pathological fracture, infection, and insufficient bone healing. Methodology: The ratio of atorvastatin to β-TCP will be 0.1 mg: 14 mg, which was the methodology adopted by Gouda et al, based on the methodology of Nyan et al.

Interventions

PROCEDURECyst enucleation and bone grafting

cyst enucleation followed by bone grafting the residual bone defects using Atorvastatin combined with β-TCP.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A case series study.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

1. Male and female patients 2. Patients 18 to 40 years old 3. Radicular cyst with a maximum diameter from 1.5 to 4.0 cm; 4. Focal teeth were preserved with root canal treatment; 5. No previous surgical treatment of the cyst site; 6. No evidence of acute inflammation; 7. In good physical status and oral health; 8. Regular attendance at control visits

Exclusion criteria

1. Patients \< 17 years old 2. Radicular cyst with a maximum diameter \< 1.5 cm. 3. Pregnancy or lactation 4. Aggregate systemic pathologies such as diabetes, thyroid disorders, and bone metabolism diseases, among others; 5. Patients taking calcium, bisphosphonates, glucocorticoids, or other drugs that can interfere with the metabolism of bone; 6. Patients with uncontrolled periodontal conditions, endodontic conditions, and other oral disorders; 7. Heavy smokers (10 cigarettes/day or more)

Design outcomes

Primary

MeasureTime frameDescription
The Rate of shrinkage of the residual bone defect3 moths post-operatively and 6 months post-operativelythe shrinkage of the residual bone defects after bone grafting, measured from the following formula: pre-operative cyst volume - 3/6 months post-operative defect volume/pre-operative cyst volume x 100%. it will be measured radiographically using CBCT through manual segmentation

Secondary

MeasureTime frameDescription
Incidence of Inflammation at the grafted site1 week post-operatively, 3 months post-operatively and 6 months post-operativelyany signs of inflammation; edema, redness or discharge

Countries

Egypt

Contacts

Primary ContactYara Mahmoud
yara.mahmoud@dentistry.cu.edu.eg01100764737
Backup ContactMohamed Mosa
mohamed.mosa@dentistry.cu.edu.eg

Outcome results

None listed

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