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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00236132
Other study ID # IRB #01-02-FB-0032
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 10, 2005
Last updated October 11, 2007
Start date August 2001
Est. completion date December 2008

Study information

Verified date October 2007
Source Children's Health System, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The main goal of the pectus multicenter outcomes study is to document the utility of PEx repair in improving health and quality of life and to test the prevailing belief that the two predominant surgical procedures currently in use for PEx repair are essentially equivalent in terms of long-term outcomes.

We believe the uncertainty about the impact of PEx on cardiopulmonary function is due to part to the fact that the previous studies have not measured the physiological parameters mostly likely affected by the defect. A protocol to test this was developed. Thus, we propose to use these measures as well as conventional output of progressive exercise test to examine cardiopulmonary function before and after surgical repair of PEx within the context of the original study.


Other known NCT identifiers
  • NCT00275470

Recruitment information / eligibility

Status Active, not recruiting
Enrollment 360
Est. completion date December 2008
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 3 Years to 21 Years
Eligibility Inclusion Criteria:Haller index by thoracic computed tomography (CT) scan of 3.2 or greater, has decided to have surgery to repair PEx, Written informed consent obtained from the parent or guardian of the subject,or, fro subjects 18-21 years, from the subject him(her)self, and assent of the child.

Exclusion Criteria:Pectus carinatum, Poland's syndrome or other comlex chest wall anomaly,Previous repair of PEx by any technique, Previous thoracic surgery, Congenital heart disease, Bleeding dyscrasia, History of major anesthetic risk factors such as malignant hyperthermia, Pregnancy, Surgical repair to be performed with bar other than stainless steel.

Study Design

N/A


Related Conditions & MeSH terms


Locations

Country Name City State
Canada The Hospital for Sick Children Toronto Ontario
United States John Hopkins Hospital Baltimore Maryland
United States Children's Hospital Boston Boston Massachusetts
United States Children's Hospital Medical Center Cincinnati Ohio
United States Children's Medical Center Dallas Dallas Texas
United States Kapi'olani Medical Center for Women and Children Honolulu Hawaii
United States The Children's Mercy Hospital Kansas City Missouri
United States Children's Hospital Of Wisconsin Milwaukee Wisconsin
United States Yale New Haven Children's Hospital New Haven Connecticut
United States Children's Hospital of New York -Presbyterian New York New York
United States Childern's Hospital of The King's Daughters Norfolk Virginia
United States All Children's Hospital St Petersburg Florida

Sponsors (2)

Lead Sponsor Collaborator
Children's Health System, Inc. Walter Lorenz Surgical Corporation

Countries where clinical trial is conducted

United States,  Canada,