- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07312448
Comparative Analysis Of Modified Vs. Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum " (PE)
Single-Center Retrospective Comparative Analysis Of Modified Vs. Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum "
Although the NUSS technique has become the standard minimally invasive procedure for correcting this deformity, there is a lack of comparative data between the classic and modified NUSS techniques. This research aims to fill this gap by comparing these two methods in terms of various outcomes, such as operative time, postoperative pain control, length of stay in the intensive care unit, and overall cosmetic results.
This study addresses the need to optimize surgical techniques to improve patient outcomes. By evaluating these two approaches, the research seeks to provide insights that could lead to better management strategies for patients with pectus excavatum, potentially influencing future clinical practices.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Isabelle TALON, MD, PhD
- Phone Number: 33 3 88 12 72 96
- Email: Isabelle.TALON@chru-strasbourg.fr
Study Locations
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-
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Strasbourg, France, 67091
- Recruiting
- Service de Chirurgie Pédiatrique - Réanimation - CHU de Strasbourg - France
-
Contact:
- Isabelle TALON, MD, PhD
- Phone Number: 33 3 88 12 72 96
- Email: Isabelle.TALON@chru-strasbourg.fr
-
Principal Investigator:
- Isabelle TALON, MD, PhD
-
Principal Investigator:
- Shaima AL SUDAIRI, MD
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients aged 11 to 18 years.
- Patients who underwent surgery between 2010 and 2024 using either the classic or modified Nuss technique. - Patient with a Haller index of 2.25 or higher.
Exclusion Criteria:
- Patients with a Haller score below 2.25.
- Patients who have undergone surgery using alternative techniques such as Ravitch or modified Ravitch.
- Patients under 11 years of age or over 19 years of age.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Operating time (in minutes)
Time Frame: Operating time (in minutes)
|
Comparaison Of Modified Vs.
Classical Nuss Technique In The Surgical Correction Of Pectus Excavatum in terms of operating time criterion (in minutes)
|
Operating time (in minutes)
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9450
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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