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Clinical Trials in Egypt / NCT06850194
Recruiting Not applicable

Vertical Ramus Osteotomy With Iliac Graft Versus Sagittal Split Osteotomy

NCT06850194 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-02-15
Last updated
2025-02-28

Condition(s) studied

Mandibular Deficiency

Investigational drug(s) / intervention(s)

vertical ramus osteotomy with iliac graftbilateral sagittal splitting osteotomy

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

bilateral sagittal splitting osteotomy: all patients in this group will undergo to bilateral sagittal split osteotomy to correct the sever mandibular deficiency

Study summary

* 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 )

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beni-Suief University Beni-seuf Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06850194 on ClinicalTrials.gov ↗ ← All trials in Egypt