Actively Recruiting
Zinc Incorporated Bovine Derived- Hydroxyappatite Xenograft in Immediately Placed Implant
Led by Suez Canal University · Updated on 2025-09-23
16
Participants Needed
1
Research Sites
64 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to evaluate Clinical and radiographic effect of zinc incorporated bovine derived hydroxyapatite xenograft and bovine hydroxyapatite xenograft alone for immediately placed implant
CONDITIONS
Official Title
Zinc Incorporated Bovine Derived- Hydroxyappatite Xenograft in Immediately Placed Implant
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult male or female patients aged between 21 and 50 years who require replacement of one or more non-restorable teeth in the lower jaw
- Adequate bone dimensions at the implant site including ridge width of at least 6 mm
- Availability of at least 3 mm of sound subapical bone
- Presence of an intact labial bone plate
- No evidence of periapical infection on cone beam computed tomography or clinical exam
- Peri-implant gaps larger than 1.5 mm
- Physically healthy with no systemic diseases
You will not qualify if you...
- Smokers
- Patients with parafunctional habits like bruxism or clenching
- Poorly controlled systemic diseases preventing anesthesia or surgery
- Patients undergoing chemotherapy, radiotherapy, or who are immunocompromised
- Pregnant or breastfeeding women
- Patients allergic to zinc
- Patients who have taken antibiotics in the past 6 months
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Suez canal university
Suez, Egypt
Actively Recruiting
Research Team
I
Ibrahim Montaser, General Dental Practitioner
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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