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Observational Comparison of Tooth-borne, Bone-borne and Hybrid Distraction Following SARPE.

NCT04670211 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2021-04-20

No results posted yet for this study

Summary

The investigators will perform a prospective, non-randomized observational study. The aim of this study is to evaluate stability of tooth-borne, bone-borne and hybrid expansion following SARPE by using data collected according to the existing SARPE follow-up protocol. The insights of this study might elucidate the preferred expansion technique and improve surgical technique.

Conditions

  • Malocclusion

Interventions

DEVICE

maxillary distractor

the type of maxillary distractor: tooth-borne, bone-borne or hybrid distractor

Sponsors & Collaborators

  • ZOL

    lead OTHER

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-05-01
Primary Completion
2023-12-31
Completion
2023-12-31

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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 NCT04670211 on ClinicalTrials.gov