- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03086499
Clustering Among the Clinical Profiles of Patients With Pectus Excavatum (PECTUS-cluster)
April 6, 2017 updated by: University Hospital, Montpellier
The primary objective of this study is to describe the relative distances between patient clinical profiles (i.e.
patient clustering) in multivariate space.
Study Overview
Status
Completed
Conditions
Detailed Description
Observational data will be collected from patient files and submitted to clustering analyses.
Then clusters will be compared.
Study Type
Observational
Enrollment (Actual)
55
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Montpellier, France, 34295
- Centre Hospitalier Universitaire de Montpellier
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients with pectus excavatum having consulted at the Montpellier University Hospital and who have had corrective surgery.
Description
Inclusion Criteria:
- Adult patient with pectus excavatum
- The patient has had corrective surgery
Exclusion Criteria:
- The patient has expressed opposition to the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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The study population
Patients with pectus excavatum having consulted at the Montpellier University Hospital and who have had corrective surgery.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The number of clusters found
Time Frame: Day 0 (transversal, retrospective study)
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The number of clusters found among clinical profiles
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Day 0 (transversal, retrospective study)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Jean Philippe Berthet, MD, PhD, University Hospital, Montpellier
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 25, 2017
Primary Completion (Actual)
March 30, 2017
Study Completion (Actual)
March 30, 2017
Study Registration Dates
First Submitted
March 16, 2017
First Submitted That Met QC Criteria
March 16, 2017
First Posted (Actual)
March 22, 2017
Study Record Updates
Last Update Posted (Actual)
April 10, 2017
Last Update Submitted That Met QC Criteria
April 6, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RECHMPL17_0094
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
NC
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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