Actively Recruiting
Prospective Outcomes of Guided Equator Overdentures
Led by Menoufia University · Updated on 2025-09-29
40
Participants Needed
1
Research Sites
169 weeks
Total Duration
On this page
Sponsors
M
Menoufia University
Lead Sponsor
M
Mansoura University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This prospective clinical study evaluated the 3-year performance of mandibular implant-supported overdentures (IODs) placed using a fully guided static computer-assisted implant surgery (CAIS) protocol. Primary outcomes included implant survival, peri-implant soft tissue health, and marginal bone loss. Findings provide evidence for the predictability of digital surgical workflows in removable prosthodontics.
CONDITIONS
Official Title
Prospective Outcomes of Guided Equator Overdentures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Completely edentulous mandible requiring implant-supported overdenture rehabilitation
- Adequate bone volume to accommodate four implants in a quadrilateral configuration, confirmed by cone-beam computed tomography (CBCT)
- Age between 40 and 75 years
- Good general health with no systemic contraindications to implant surgery
- Willingness and ability to provide informed consent
- Commitment to attend all scheduled follow-up visits over the 3-year study period
You will not qualify if you...
- Uncontrolled systemic diseases (e.g., diabetes mellitus, osteoporosis)
- History of radiotherapy in the head and neck region
- Untreated oral infections or severe periodontal disease
- Poor oral hygiene or inability to comply with maintenance protocols
- Heavy smoking (>10 cigarettes/day) or alcohol abuse
- Known allergy or intolerance to materials or medications used in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Faculty of Dentistry
Shibīn al Kawm, Egypt
Actively Recruiting
Research Team
M
Mohammed A. El-Sawy, PhD
CONTACT
M
Mohammed T. Khater, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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