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Effect of simvastatin gel on periodontitis

Clinical evaluation of the effect of allograft alone, or in combination with simvastatin gel in the treatment of mandibular class II furcation defects in human

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016112631116N1
Enrollment
10
Registered
2017-01-07
Start date
2015-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Furcation involvement class 2 mandible molars (periodontitis). Periodontal disease, unspecified

Interventions

Intervention 1: Intervention group: allograft and membrane and simvastatin gel are used. After local anesthesia and incision in the target area, flap were reflected, debridemant was performed, then al
Treatment - Surgery
Intervention group: allograft and membrane and simvastatin gel are used. After local anesthesia and incision in the target area, flap were reflected, debridemant was performed, then allograft with sim
Control group: allograft with placebo gel. After local anesthesia and incision in the target area, flap were reflected, debridemant was performed, then allograft put in the defect, membrane adapted o

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- presence at least 1 pair of first or second molar of mandible bilaterally accompanied with fraction involvement class 2 with less or equal 3 mm horizontal penetration of probe. 2- presence at least 2 mm keratinized gingiva around each tooth. Exclusion criteria: 1- smoking. 2- history of systemic disease. 3- pregnant or breast feeders. 4- history of antibiotic consumption within 2 months. 5- hx of periodontal treatment within 6 months. 6- hx of hypersensitivity to statins. 7- pt with statin treatments. 8- aggressive periodontitis. 9- tooth mobility grade 3. 10- pulp-pathology and incomplete RCT or PA lesion. 11- poor oral hygiene.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical Attachment Level. Timepoint: preoperative, during and 6 months post surgery. Method of measurement: probe and CBCT.

Secondary

MeasureTime frame
Recession. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe.;Bone Fill. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe and CBCT.;Probing pocket depth. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe and CBCT.;Horizontal penetration in the Furca. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe and CBCT.;Bleeding Index. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe.;Plaque Index. Timepoint: before Surgery- during Surgery- 6 month after. Method of measurement: Periodontal probe.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farin Kiany Yazdy

Shiraz Dentistry School

farinkiany@yahoo.com+98 71 3628 9919

Outcome results

None listed

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