Comparative Analysis of 2 Bone Graft Materials in Socket Preservation
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-50
SponsorPharos University in Alexandria
About this trial
Socket preservation procedures after tooth extraction have been designed and implemented to maintain the volume of the bone and gingival tissues, which can decrease following the extraction of the teeth. In this clinical trial we will compare clinically and histologically the effectiveness of two distinct bovine bone graft materials; an allograft and a xenograft, in alveolar ridge preservation procedures following tooth extraction .
Eligibility criteria
This trial accepts healthy volunteersQualifiers
• Systemically healthy individuals
Non-smokers
Age between 21 and 50 years
Indicated for tooth extraction and socket preservation
Disqualifiers
• Stage III or IV periodontitis
Active periodontal or periapical infection
Severely resorbed sockets (buccal bone height <5 mm)
Smoking more than 10 cigarettes per day
Trial design
Design model
Parallel
Treatments tested in this trial
Socket Preservation with Graft Material Allograft
Procedure/SurgerySocket preservation will be performed after tooth extraction using graft material Allograft or Xenograft according to standard surgical protocol.
Treatment groups
18 Participants
are divided into 2 treatment groupsGroup A: Allograft GroupExperimental treatment 1 intervention
Group B: Xenograft GroupExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Change in buccolingual ridge width
Difference in ridge width measured clinically and radiographically between baseline and 2-3 months post-extraction
Time frame
Baseline to 2-3 monthsSecondary outcomes
1
Histomorphometric outcomes
Percentage of new bone formation, residual graft material, and soft tissue/marrow space
Time frame
2-3 monthsSponsors and contacts
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Source ClinicalTrials.gov