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Recruiting NCT06850194

Vertical Ramus Osteotomy With Iliac Graft Versus Sagittal Split Osteotomy

No phase Interventional Mandibular Deficiency

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: vertical ramus osteotomy with iliac graft, bilateral sagittal splitting osteotomy.
Who it may be relevant to
Registry conditions: Mandibular Deficiency. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluating the Efficacy of Vertical Ramus Osteotomy With Iliac Graft Versus Bilateral Sagittal Split Osteotomy for the Correction of Mandibular Deficiency in Skeletal Class II Cases Management. A Randomized Controlled Trial

Overview

* Patients will be collected from faculty of dentistry * bilateral vertical ramus osteotomy (VRO )with iliac graft group (group I):- 10 patients will be treated via VRO and iliac crest or * bilateral sagital spilt osteotomy (BSSO) group (group II):- 10 patients will be treated via BSSO * All patients will be studied by comprehensive clinical oral and maxillofacial examination and lateral cephalometric radiographic analyses, within 1 week before the surgery (T0), immediately after the surgery (T1), and 6 months after surgery (T2). * All lateral cephalometric radiographs and clinical photographs must be standardized for all cases. * After pre-surgical orthodontic treatment , a lateral cephalograph Will be obtained for planning the surgical movement of both jaws * Surgical models and surgical stent will be fabricated. * All surgical procedures will be performed under nasal intubation and general anesthesia to surgically reposition the maxilla in standard LeFort I setback fosteotomy; the BSSO group will be underwent BSSO, and VRO group will be underwent VRO * The bony segments will be fixed in the new position with the use of custom made plates (specific for each patient )

Interventions

  • Procedure vertical ramus osteotomy with iliac graft
    in the VRO group all patient will undergo vertical ramus osteotomy surgery with iliac graft to correct the sever mandibular defficiency
  • Procedure bilateral sagittal splitting osteotomy
    all patients in this group will undergo to bilateral sagittal split osteotomy to correct the sever mandibular deficiency

Primary outcome measures

  • skeletal stability [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • patients with age above 18 years old suffered from skeletal class II with severe mandibular deficiency

Exclusion criteria

  • patients with chin deviation,
  • severe temporomandibular joint (TMJ) symptoms.
  • Sever periodontal disease
  • pregnancy,
  • previous mandibular surgery,
  • inability to follow-up for the study protocol

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Beni-Suief University — Beni-seuf

Identifiers

NCT: NCT06850194 · 111

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗