Effect of Atorvastatin gel on clinical and histological parameters in socket preservatio

Not Applicable

Recruiting

Conditions: socket preservation.
Partial loss of teeth, unspecified cause
K08.40

Registration Number: IRCT20110109005570N11

Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 15

Inclusion Criteria

Patient with healthy systemic condition
Single-rooted or double-rooted teeth
Presence of sound buccal and lingual plates after tooth extraction
Presence of a minimum of 10 mm vertical bone height without invading the adjacent critical structures,

Exclusion Criteria

Allergy to collagen membrane
Severe untreated periodontitis
Acute infection or pus at the extraction site

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ength of socket. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Periodontal probe.;Width of socket. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Periodontal probe.;Width of keratinized gingiva. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Periodontal probe.;Thickness of gingiva. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Periodontal probe.;Percent of ossification of alveolar socket. Timepoint: 2 months after the intervention. Method of measurement: Histological evaluation.;Thickness of new trabecula. Timepoint: 2 months after the intervention. Method of measurement: Histological evaluation.

Secondary Outcome Measures