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Mandibular Reconstruction Bone Plate

NCT06099431 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2025-04-10

No results posted yet for this study

Summary

The purpose of this study is to evaluate the reliability of using mandibular osteosynthesis a 2.3mm reconstruction bone plate in the maintenance of the space, contour, and mandibular bone preservation during marginal mandibular resection.

Conditions

  • Mandible Tumor

Interventions

PROCEDURE

Mandibular marginal resection and reconstruction

Intraoral buccal and lingual incisions 2-3 mm away from the free gingival margins were carried out around the teeth to be included in the resection. The osteotomy lines were marked using a long shank surgical tapered fissure bur. The osteotomies completed and the resected segment was removed.

DEVICE

mandibular osteosynthesis a 2.3mm reconstruction bone plate

a 2.3 mm reconstruction bone plate was then fit in place and fixed to both the proximal and distal segments

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Principal Investigators

  • Mohamed K Allam, Ass prof · Tanta University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-22
Primary Completion
2025-12-10
Completion
2025-12-30

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 NCT06099431 on ClinicalTrials.gov