Mode
Text Size
Log in / Sign up
Phase 2 N=10 Treatment

Magnetic Mini-Mover Procedure to Treat Pectus Excavatum

Pectus Excavatum

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Sep 2012
Primary outcome: Primary: Affect on Cardiac Activity — 0 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Magnetic Mini-Mover Procedure (3MP) (Device); Magnatract (external magnet in a removable external brace) (Device); 3MP (Magnetic Mini-Mover Procedure) (Procedure)
Age
Pediatric · 8+ yrs
Sex
All
Sponsor
University of California, San Francisco
Primary completion
May 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Affect on Cardiac Activity
PRIMARY
Damage/Discoloration to Skin
PRIMARY
Efficacy: Patient Satisfaction
3.7
PRIMARY
Efficacy: Patient Recommendation of Treatment
4.2
SECONDARY
Patient Compliance
16

Summary

This is a medical research study. The study investigators have developed a method to gradually repair pectus excavatum (sunken chest) deformity by placing a magnet on the sternum (breastbone) and then applying an external magnetic force that will pull the sternum outward gradually. Potential candidates for this study are children and adolescents with a previously diagnosed congenital pectus excavatum (sunken chest) deformity who are otherwise healthy and are seeking corrective surgery for their condition. They will be residents of the U.S. and between the ages of 8 and 14 years of age. Potential candidates and their families will have already been counseled about this condition and about the standard way to repair this deformity. The purpose of this study is to test what effects, good and/or bad, placing an external/internal magnetic device has on correcting pectus excavatum deformity in children, and the safety of using such a device for treatment.

Eligibility Criteria

Residents of the United States with previously diagnosed pectus excavatum who are referred to the UCSF Pediatric Surgery Service for evaluation and treatment will be considered for participation in this study. Only patients with moderate to severe pectus excavatum who meet all the inclusion criteria will participate. The patient and family will be fully counseled and consented about the risks and benefits of participation in the study, and will be asked to sign an informed consent reviewed and approved by the UCSF Committee on Human Research.

Inclusion Criteria

  • Resident of the U.S.;
  • Otherwise healthy male or female with pectus excavatum deformity;
  • Between 8 and 14 years of age;
  • Pectus Severity Index > 3.5 (normal 2.56); and
  • Ability to read and speak English.

Exclusion Criteria

  • Other congenital anomalies (including significant skeletal anomalies such as scoliosis, bony fusion involving the cervical vertebrae) not directly related to pectus excavatum;
  • Bleeding disorders;
  • Heart disease (including arrhythmia);
  • Persons with active implantable medical devices (AIMD) such as pacemakers;
  • Persons with a relative(s) or close family friend(s) living within their households and having a pacemaker;
  • Persons with arteriovenous malformations;
  • Chest deformity more complicated than pectus excavatum (e.g.. Poland syndrome);
  • Persons for whom a foreign body implant would pose a risk (e.g., immunodeficiency);
  • Persons at increased risk for general anesthesia (e.g., history of malignant hyperthermia);
  • Respiratory conditions that have required steroid treatment (e.g., prednisone)in the last 3 years;
  • Pregnancy;
  • Inability to understand or follow instructions;
  • Refusal to wear the external brace;
  • Inability to obtain pre-approval (authorization) from the patient's insurance carrier; and
  • Inability or refusal to return to UCSF for weekly follow-up visits for the first month after surgery.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00466206). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search