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Efficacy of Transverse Maxillary Expansion With AMCOP Preformed Appliances

StatusEnrolling by Invitation
PhaseNot applicable
Started
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Record status
This record was last updated April 16, 2025 (before its estimated February 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Trial status: Recruiting to Enrolling by Invitation
    • Primary and study completion dates: Mar 2026 to Feb 2026
    • Start date changed from estimate of Mar 2025 to Mar 15, 2025
    • Site details revised
    v3
  2. Trial status: Not Yet Recruiting to Recruiting
    • Secondary endpoints: 14 to 15
    • Site details revised
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The present study aimed to investigate the cross-sectional effect of Class I AMCOP devices in patients of all possible skeletal types from both vertical skeletal pattern (normodivergent, hyperdivergent, hypodivergent) and sagittal skeletal pattern (skeletal Class I, skeletal Class II, skeletal Class III). The criterion for choosing patients was determined by the protocol of using these devices, which is to always perform an AMCOP First Class phase with the aim of improving transverse coordination of the arches, Spee's Curve and Wilson's Curve.
Trial Details
NCT Number NCT06864949
Lead Sponsor University of Pavia
Conditions
(from sponsor)		 Transverse Maxillary Deficiency
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov