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Evaluation, the Histomorphometric Study of Nanocrystalline Hydroxyapatite (Nano Bone) Wif Lovastatin in the Preservation of the Tooth Socket

the Histomorphometric Study of Nanocrystalline Hydroxyapatite (Nano Bone) With Lovastatin in the Preservation of the Tooth Socket

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03981601
Enrollment
20
Registered
2019-06-11
Start date
2018-02-22
Completion date
2019-07-30
Last updated
2019-06-11

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

Conditions

Bone Loss

Brief summary

Twenty patients referring to periodontics department of Boroujerd Azad university of dentistry after obtaining consent to participate in the research project, which have more than 20 teeth, are over 18 years old and require socket preservation surgery to tooth extraction for the periodontal problem, caries or Fractures were selected.

Detailed description

twenty healthy patients referring to periodontics department of Boroujerd Azad university of dentistry after obtaining consent to participate in the research project, which has more than 20 teeth, are over 18 years old and require socket preservation surgery to tooth extraction for the periodontal problem, caries or Fractures were selected. moreover, divided the socket randomly to two groups(A, B)including A: bone graft with lovastatin and B: bone graft alone, after 3 months with trephine will collect the samples. following the histomorphometric analysis.

Interventions

DRUGLovastatin 40 MG

after tooth extraction, put teh lovastatin40 mg wif bone graft wifin tooth socket

PROCEDUREwithout drug with Bone graft

after tooth extraction, put teh bone graft wifin tooth socket

Sponsors

Islamic Azad University, Sanandaj
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. at least 18 years old 2. tooth fracture, root caries 3. Patients are volunteered for placement of the implant

Exclusion criteria

1. systemic diseases 2. Pregnancy and breastfeeding 3. malignancy, radiation therapy, 4. history of periodontal surgery during the six months ago. 5. medicine(phosphonates, antibiotic,...)

Design outcomes

Primary

MeasureTime frame
Socket preservation with Lovastatin as evaluated by the amount of bone formation volume3 month

Countries

Iran

Contacts

Primary ContactAmirhossein Farahmand, Assistant Prof
perio-implant@hotmail.com+98 912 404 0359

Outcome results

None listed

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