MedTrace Logo

Inter Flex Three Dimensional Plate in Management of Mandibular Fracture RCT

NCT07263893 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2026-01-22

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if The use of a 3D-designed Inter-flex plate will achieve safe and desirable anatomical \& functional restoration with reduced operative time in mandibular fracture,

* Improvement of occlusal and inter-cuspal relation in addition to stabilized intra-fragmentary mobility,
* Offer greatest resistance to displacement
* shows most favorable biomechanical behavior

Conditions

  • Mandibular Fracture Treatment

Interventions

PROCEDURE

Group I :site with mandibular fracture will be treated with custom made Inter-flex three dimensional plate in site of mandibular fracture

site with mandibular fracture will be reduced and fixation will be done .visibility using custom made Inter-flex three dimensional plate plates in Group I and fixation using custom made Inter-flex three dimensional according to champ's lines of osteo-synthesis in Group I. closure of the surgical field with vicryl suture material (90% glycolide and 10% L-lactide: Ethicon part of Johnson \& Johnson Int, US.).

Sponsors & Collaborators

  • Suez Canal University

    lead OTHER

Principal Investigators

  • Mohamed Ah Elsholukamy, Professor · Suez Canal University

  • Mohamed Na Gad Elhaq, lecturer · Suez Canal University

  • Maurice Fe khalil, consultant · Mataria Teaching Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-01
Primary Completion
2026-12-01
Completion
2026-12-03

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07263893 on ClinicalTrials.gov