CompletedNot Applicable

Comparison Between Two Techniques to Reposition the Maxilla After le Fort 1

Egypt14 participantsStarted 2022-11-15

Plain-language summary

clinical and radiographic comparison between novel locating guide design with pre-bent titanium plates and 3d printed intermediate wafer to reposition the maxilla after Le Fort 1 osteotomy in orthognathic surgery (randomized controlled clinical trial)

Who can participate

Age range18 Years – 42 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * All patients requiring Le Fort I osteotomy will be selected including those suffering from skeletal malocclusion (Class II or Class III), midface hypoplasia or vertical maxillary excess. Exclusion Criteria: cleft lip and palate. skeletal disharmony due to trauma or severe facial asymmetry. significant medical condition.

What they're measuring

Radiographic evaluation of accuracy by superimposition

Timeframe: 2 weeks

The surgery duration

Timeframe: 1 week

Trial details

NCT IDNCT06132906

SponsorAlexandria University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-10-01

View on ClinicalTrials.gov More Dentofacial Deformities trials