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CompletedNCT06588075Updated Feb 18, 2026

A Full Digital VS Conventional Protocol in Management of Zygomatico-Maxillary Complex Fracture

An interventional study of Reduction and fixation of zygomatico- Maxillary complex fracture using a full digital work flow and Reduction and fixation of zygomatico- maxillary complex fracture using a conventional free hand protocol in Zygomatic Fractures, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-18.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

this study aims To evaluate The Accuracy of Zygomatico- Maxillary Complex (ZMC) Fracture reduction and fixation Using customized Patient-Specific implant and patient-specific predictive holes surgical guide Versus Conventional Technique of reduction and fixation.

Read the detailed description

The ZMC has multiple points of articulation with the craniofacial skeleton making accurate assessment of reduction at all articulations intraoperative in multiple planes very challenging and the interference of soft tissue edema and a narrowed visual field increases the possibility of intraoperative overcorrection or underestimation of pre-injured position of all fracture lines at the same time resulting in a suboptimal reduction. As a trial to maximize the benefits of digital planning carrying the plan into a real operating room using a patient-specific surgical guide to predrill screw holes and guide patient-specific implants during fixation according to the planning depend on CT scan.

02

Conditions studied

  • Zygomatic Fractures

Keywords

  • Zygomatic fracture
  • computer guided surgery
  • patient specific implant
  • predictive holes surgical guide
  • Zygomatico-Maxillary complex fracture
03

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Zygomatic Fracture Types III, IV, V, VII, and VIII according to Rowe and Killey's classification.
  • Age range (18-60 years).
  • Patients are willing for the surgical procedure and follow-up, with informed consent

Exclusion criteria

Exclusion Criteria:

  • Zygomatic Fracture Type I, II according to Rowe and Killey's classification.
  • Patients with contraindications for general anesthesia.
  • Patient on radiotherapy.
  • Patients suffer from bone disease.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    study group

    all cases that will be allocated in this group will undergo treatment using a full digital protocol depending on planning software and the planning will be carried out into the operating room using 3D printed predictive holes surgical guides to determine accurately the optimum position of customized plates

    Procedure: Reduction and fixation of zygomatico- Maxillary complex fracture using a full digital work flow

  • Active comparator
    control group

    patients in this group will be treated using a conventional protocol of reduction depending on visualization intraoperative and tactile sensation and will be fixed using a stock miniplates and screws.

    Procedure: Reduction and fixation of zygomatico- maxillary complex fracture using a conventional free hand protocol

Interventions

  • ProcedureReduction and fixation of zygomatico- Maxillary complex fracture using a full digital work flow

    All surgeries will be carried out under general anesthesia the fracture lines will be exposed then For the study group: following the exposure of all fracture lines , anatomically seated bone-supported predictive holes surgical guides will be inserted on the bone segments with intimate contact. Each segment hole will be drilled according to the predesigned predictive holes guide. The fractured segments will then be reduced and fixed using titanium miniplates customized for the patient and screws at least two screws for each fracture segment. then closure in layers will be performed using absorbable vicryl for deep layers and intraoral sutures and non-absorbable polyproline for skin closure.

  • ProcedureReduction and fixation of zygomatico- maxillary complex fracture using a conventional free hand protocol

    For the control group: all cases will be treated under general anesthesia and the fracture lines will be exposed then the conventional protocol of treatment depend mainly on visualization of the fracture line and tactile sensation of the operator intra-operative during reduction procedure and the fixation of fractured segments will be done using titanium miniplates and screws then closure in layers will be performed.

05

What researchers measure

Primary outcomes

  1. Zygomatic reposition

    the accuracy of zygomatic bone reduction and fixation using postoperative CT scan

    Time frame: immediate postoperative

Secondary outcomes

  1. intraoperative time

    duration of operation using stopwatch

    Time frame: during the operation

  2. paresthesia

    sensation in the area supplied by the infraorbital nerve using a 2 points discrimination test

    Time frame: pre operative, immediate postoperative and 6 months post operative

  3. patient satisfaction

    patient aesthetic satisfaction will be measured using a visual analogue scale from 0 to 10 in a questionnaire form, zero mean not satisfied at all and 10 is the maximum satisfaction.

    Time frame: 6 months postoperative

06

Study locations

1 site
  • Cairo university
    Giza, 12613, Egypt
07

References and documents

Individual participant data

Plan to share: Undecided — the data will be available from the corresponding author upon reasonable request.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06588075
Lead sponsor
Cairo University
Responsible party
Dina Ayman Fayek (Assistant lecturer in Oral and Maxillofacial department in Future university in Egypt, Cairo University) — Principal investigator
First posted
Sep 19, 2024
Start date
Sep 4, 2024
Primary completion
Jun 1, 2025
Completion
Jan 1, 2026
Last update
Feb 18, 2026

Study contacts

Dina Ayman Fayek, M.Sc
principal investigator · Assistant lecturer oral and maxillofacial surgery department Future university in Egypt

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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