Evaluation of blood components on healing of extracted teeth site
Not Applicable
- Conditions
- Z40.9ridge preservation.Encounter for prophylactic surgery, unspecified
- Registration Number
- IRCT20160815029369N2
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 26
Inclusion Criteria
Patient should be at least 18 years old
Lack of any systemic disease
Patient should not use any immunosuppressive drug, corton and any drug that can affect the bone metabolism
Intact socket or sockets which have less than 50% dehiscence
Exclusion Criteria
Over than 25 %plaque index
Periodontitis
Pregnant women
Teeth with acute or chronic peri-apical lesions
Traumatic tooth extraction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in ridge height and width. Timepoint: Measuring of ridge width and height immediately and 8 weeks after extraction. Method of measurement: radiographic analysis will have been performed on DICOM file.;New bone formation. Timepoint: New bone formation in histologic view 8 weeks after extraction. Method of measurement: Histologic evaluation with Microbin software .
- Secondary Outcome Measures
Name Time Method Ridge width in 25,50 and 75 % of socket depth. Timepoint: immediately after tooth extraction and 8 weeks later. Method of measurement: evaluation on DICOM file.;Height of buccal plate. Timepoint: immediately after tooth extraction and 8 weeks later. Method of measurement: evaluation on DICOM file.;Height of lingual plate. Timepoint: immediately after tooth extraction and 8 weeks later. Method of measurement: evaluation on DICOM file.