CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 15 enrolled
Drug / intervention
Magnetic Mini-Mover Procedure (Magnimplant)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01327274
NCT01327274N/ACompleted

Phase 3 Multicenter Study of Magnetic Mini-Mover for Pectus Excavatum

Michael Harrison·interventional·Posted Apr 1, 2011·Updated Nov 8, 2018

In Brief

A clinical study evaluating Magnetic Mini-Mover Procedure (Magnimplant) for Pectus Excavatum. Completed, enrolled 15 participants across 3 sites.

Detailed Summary

This study is a Phase 3, multicenter, non-randomized study to evaluate the safety and efficacy of the next-generation outpatient Magnetic Mini-Mover Procedure (3MP) in 15 patients aged 8-14 years for the correction of pectus excavatum ('sunken chest'). 3MP for pectus excavatum uses a magnetically coupled implant to pull the sternum forward and gradually remodel the deformed costal cartilage. The Funding Source for this trial is the FDA Office of Orphan Products Development (Grant #R01 FD003341).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedApr 1, 2011
Enrollment StartDec 1, 2011
Primary CompletionNov 1, 2016
Study CompletionMay 1, 2018
TodayJul 2, 2026
Enrollment to primary: 4.9 yearsPosted 15.3 years ago

Interventions

Magnetic Mini-Mover Procedure (Magnimplant)device

This is a non-randomized study in which otherwise healthy patients, ages 8-14, with severe pectus excavatum (PSI \> 3.5) will undergo the Magnetic Mini-Mover procedure outpatient surgery. The Magnimplant or Magnetic Mini-Mover device implant will surgically implanted on the sternum. Patients will be required to wear a custom-fitted orthotic brace, which houses the external magnet and records brace-wear compliance. They will undergo brace treatment for 18-24 months, enough to attempt to improve their PSI (\< 3.25). Patients will be seen in clinic at least monthly until treatment is complete and the magnimplant device will be explanted from their sternum.