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Treatment of Severe Alveolar Defect With Calcium Sulfate and Simvastatin

Efficacy of Calcium Sulfate and Simvastatin Drug Delivery System in Combination with Non Autogenous Bone Graft in the Treatment of Severe Alveolar Horizontal Defect: A clinical, histological and histomorphometric study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190409043211N2
Enrollment
15
Registered
2020-12-02
Start date
2020-12-20
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Atrophy of alveolar ridge. Atrophy of edentulous alveolar ridge

Interventions

Intervention group: reconstructive surgery with simvastatin at a specific dose (10mg / 1gr) entrapped in calcium sulfate drug delivery system in combination with non-autogenous bone marrow.

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with horizontal defect in the alveolar ridge with overall thickness less than 4 mm

Exclusion criteria

Exclusion criteria: Patients with systemic problems that affect the tissue repair process (connective tissue diseases. Kidney failure. Liver failure. Diabetes) Smokers Patients taking anti-osteoporosis drugs Lack of patient consent to participate in the study Patients of developmental age. Pregnant patients Patients with psychological problems

Design outcomes

Primary

MeasureTime frame
The amount of increase in the thickness of the alveolar ridge. Timepoint: Measurement of alveolar ridge thickness at the beginning of the study before the intervention and 4 months after the intervention. Method of measurement: Caliper with an accuracy of one tenth of a millimeter.

Secondary

MeasureTime frame
Percentage of viable bone to total graft volume in the reconstructed area. Timepoint: 4 months after the intervention. Method of measurement: Observations under light microscope to examine the percentage of newly-formed bone.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzin Ahmadpour

Tabriz University of Medical Sciences

phoenixinfire@ymail.com+98 41 3335 5965

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026