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Comparison of the Clinical, histologic and histomorphometric of Ceno Bone ® with and without plasma rich growth factor in dental socket

Phase 3
Conditions
.
Registration Number
IRCT20100427003813N10
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Patients with non-restoring molar in the lower jaw with indications out
volunteer for performing implant
have good health
availability for follow-up
Signature of consent form

Exclusion Criteria

Patients who are not able to perform surgery
smoker
Pregnancy
Dental Infection
Patients with gingivitis or active untreated periodontitis
Patients with ankylosis of teeth
teeth with dehiscence
Diseases that affect tissue repair
Patients with certain systemic problems

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Vertical changes in dental apicoronal socket. Timepoint: before surgery,5 months after surgery. Method of measurement: stent.;Degree of inflammation. Timepoint: 5 months after surgery. Method of measurement: histology.;Trabecular thickness. Timepoint: 5 months after surgery. Method of measurement: histology.;Bone-biomaterial contact. Timepoint: 5 months after surgery. Method of measurement: histology.;Presence or absence of connective tissue in the reconstructed area. Timepoint: 5 months after surgery. Method of measurement: histology.;Percentage of remnant particles. Timepoint: 5 months after surgery. Method of measurement: histology.;Percentage of new bone formation. Timepoint: 5 months after surgery. Method of measurement: histology.;Number of blood vessels. Timepoint: 5 months after surgery. Method of measurement: histology.;Bone Vitality. Timepoint: 5 months after surgery. Method of measurement: histology.;Foreign body reaction. Timepoint: 5 months after surgery. Method of measurement: histology.
Secondary Outcome Measures
NameTimeMethod
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