Actively Recruiting
Evaluation of Zygomatic Implant Placement Accuracy Using Fully Metallic vs Resin-based Surgical Guides in Severely Atrophic Maxilla
Led by Future University in Egypt · Updated on 2026-05-07
4
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the accuracy of two types of surgical guides used to place zygomatic implants in patients with severe bone loss in the upper jaw. Zygomatic implants are longer than regular dental implants and are fixed in the cheekbone, which generally has enough bone to support them. The study focuses on patients with severely atrophic maxilla who need these special implants due to significant bone loss. The main goal is to determine whether fully metallic surgical guides or resin-based guides improve the precision of implant placement. Participants will receive zygomatic implants on both sides of the upper jaw during surgery. On one side, the implant will be placed using a fully metallic surgical guide made of nickel with CAD/CAM technology. On the other side, the implant will be placed using a resin surgical guide made from biocompatible 3D-printed material. Before surgery, patients will undergo a CT scan and digital impressions or planning to create these guides. This allows direct comparison of the two guide types within the same patient. During the study, patients will have clinical examinations and CT scans before and after surgery to plan and verify implant placement. Researchers will measure the difference between planned and actual implant positions to assess accuracy. Additional outcomes include implant stability, surgical time, and any complications during surgery. Participation involves follow-up visits and signing informed consent, with the study lasting through the implant placement and evaluation periods.
CONDITIONS
Brief Title
Evaluation of Zygomatic Implant Placement Accuracy Using Fully Metallic vs Resin-based Static Surgical Guides in Severely Atrophic Maxilla
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older with severely atrophic maxilla
- Maxillary defects caused by trauma, pathology, or previous surgery
- Candidates for zygomatic implant-supported fixed prosthesis
- Sufficient mouth opening to allow placement of zygomatic implants
- Willingness to provide informed consent and attend follow-up visits
You will not qualify if you...
- Uncontrolled systemic diseases affecting healing, such as uncontrolled diabetes
- Heavy smokers
- Previous radiotherapy or bisphosphonate treatment
- Active infection in sinus or nasal areas
- Severe parafunctional habits like bruxism
- Pregnant or lactating women
- Psychiatric disorders that affect compliance
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 4 weeks
Participants receive zygomatic implant placement using either a fully metallic or resin-based static surgical guide, with CT scans and digital impressions taken before surgery to create the guides.
1 surgical visit
Duration - Up to 4 weeks after surgery
Participants are monitored following implant placement to assess implant placement accuracy and healing progress.
Follow-up visits as scheduled
Trial Site Locations
Total: 1 location
1
Future University in Egypt
New Cairo, Cairo Governorate, Egypt, 11835
Actively Recruiting
Research Team
A
ahmed abozekry associate professor of oral and maxillofacial surgery at FUE, associate professor
A
aya magdy lecturer of oral and maxillofacial surgery at FUE, LECTURER
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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