Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07551024

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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

Post-operative Follow-up

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

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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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