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Clinical Trials/NCT03183349
NCT03183349
Unknown
N/A

Immediate Implant Placement With Platlet Rich Fibrin as Space Filling Material Versus the Use of Deprotienized Bovine Bone (Tutogen) in Maxillary Premolars. A Randomized Controlled Clinical Trial

Cairo University0 sites20 target enrollmentJuly 2016
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ConditionsImmediate Dental Implant

Overview

Phase
N/A
Intervention
Not specified
Conditions
Immediate Dental Implant
Sponsor
Cairo University
Enrollment
20
Primary Endpoint
Patient morbidity
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

20 subjects suffering from non restorable maxillary premolar teeth will be randomly devided into two groups. the selected teeth will be extracted and immeiate implants will be placed in all subjects. the first group will recieve deprotienized bovine bone (tutogen) to fill the buccal space between the implant and the bone, the second group will recieve platlet rich fibrin to fill the buccal space between the implant and the bone

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
July 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed mohamed awad elbrashy

Principal Investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • •non restorable maxillary premolars non smoker free from any systemic disease or medication that could impair normal bone healing

Exclusion Criteria

  • •any systemic disease that could affect bone healing patient with lesion related to the surgical site

Outcomes

Primary Outcomes

Patient morbidity

Time Frame: 14 days

patient pain level on pain scale using pain chart

Secondary Outcomes

  • crestal bone loss(3 months)
  • implants stability quotient(3 months)

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