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Completed Not applicable Interventional Results available

An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery

ClinicalTrials.gov ID: NCT01783483

Public ClinicalTrials.gov record NCT01783483. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 5:20 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery: A Prospective, Randomized Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to evaluate sternal bone healing following a full median sternotomy versus standard of care for sternal closure with wire cerclage. Additional outcomes on post-operative pain and analgesic usage, patient function and quality of life, and complications will also be collected. A health economics study will also be conducted, in which cost and billing data will be collected from sites participating in this clinical study.

Study identification

NCT ID
NCT01783483
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Zimmer Biomet
Industry
Enrollment
236 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2012
Primary completion
May 31, 2015
Completion
Nov 30, 2016
Last update posted
Sep 7, 2017

2013 – 2016

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Mayo Clinic Jacksonville Jacksonville Florida 32224
Florida Hospital Orlando Florida 32803
Emory University Atlanta Georgia 30308
Franciscan St. Francis Health Indianapolis Indiana 46237
University of Louisville Louisville Kentucky 40202
United Heart & Vascular Clinic, United Hospital, part of Allina Health Saint Paul Minnesota 55102
Saint Luke's Mid America Heart and Vascular Institute Kansas City Missouri 64111
Columbia University Medical Center New York New York 10032
Lenox Hill Hospital New York New York 10065
University of Toledo Toledo Ohio 43614
Temple University Hospital Philadelphia Pennsylvania 19140
Scott & White Memorial Hospital Temple Texas 76508

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01783483, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 7, 2017 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01783483 live on ClinicalTrials.gov.

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