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NCT05817526 Clinical Trial

BMAC Loaded Collagen Jumping the Gap Around Immediate Implants

Implant Site Reaction Clinical Trial

Official title:
Assessment of Collagen Loaded With Bone Marrow Aspirate Concentrate Versus Autograft on Marginal Bone Changes Around Immediate Implants in Esthetic Zone. A Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05817526
Other study ID # BMAC around immediate implants
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 25, 2023
Est. completion date December 2024

Study information
Verified date March 2024
Source Cairo University
Contact Walaa Kadry
Phone +201061527359
Email walaakadry@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study aims to evaluate the effect of utilization of BMAC/ collagen on marginal bone changes around immediate implants in the esthetic zone of maxilla. Methodology: Twenty dental implants will be installed in the esthetic zone and patients will be randomly divided into two groups: study group: The jumping gap surrounding the immediate implants will be grafted with BMAC/collagen, whereas in the control group, autograft from the chin will be used to fill the defect. Cone beam CT (CBCT) will be requested Preoperative, immediate and 4 months Postoperative for assessment of marginal bone changes around implants. .

Description:

The aim of present study is to evaluate the effect of utilization of bone marrow aspirate concentrate (BMAC) loaded on collagen on the marginal bone changes around immediate implants in the esthetic zone of maxilla. Methodology: Twenty dental implants will be installed in patients suffering from non- restorable teeth in esthetic zone. Patients will be randomly divided into two equal groups: study group: The jumping gap surrounding the immediate implants will be grafted with bone marrow aspirate concentrate loaded on collagen, whereas in the control group, autogenous bone graft from the chin will be used to fill the peri-implant defect. CBCT will be requested Preoperative, immediate and 4 months Postoperative for assessment of marginal bone changes around dental implants. .

Recruitment information / eligibility
Status Recruiting
Enrollment 20
Est. completion date December 2024
Est. primary completion date October 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patients with non- restorable teeth in esthetic zone - Patients above 18 us - Highly motivated patients. Exclusion Criteria: - patients with systemic diseases • immunocompromised patients . Patients with bleeding disorders

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• BMAC/ collagen
Bone marrow aspirate concentrate loaded on collagen in the peri-implant defect
Procedure:
• Autograft harvesting from chin
Autograft

Locations
Country Name City State
Egypt Walaa Kadry Cairo

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Marginal bone changes Buccal bone height 4 months
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