Spontaneous Pneumothorax in Adolescents (PNSA)

December 15, 2023 updated by: University Hospital, Strasbourg, France

Spontaneous Pneumothorax in Adolescents: Inventory and Management

Pneumothorax is characterized by an abnormal presence of air in the pleural cavity, that is to say between the two layers of the pleura, the membrane that surrounds the lungs and lines the rib cage. "The patient is usually seized with sudden chest pain and difficulty in breathing.

In this retrospective research, the investigators wish to carry out an inventory of the management of spontaneous pneumothorax in adolescents within the University Hospitals of Strasbourg

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Estimated)

134

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Strasbourg, France, 67091
        • Recruiting
        • Service de Chirurgie Pédiatrique - CHU de Strasbourg - France
        • Principal Investigator:
          • Isabelle TALON, MD
        • Sub-Investigator:
          • François LEFEBVRE, MD
        • Contact:
        • Sub-Investigator:
          • Soufiane ESSAMOUD, MD
        • Sub-Investigator:
          • Nizar SASSI, MD

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

  • Child
  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Patient (aged between 14-20 years old) having pontaneous pneumothorax without apparent cause and operated on at the HUS between 2010 and 2021.

Description

Inclusion criteria:

  • Adult patient (18-20 years old)
  • Minor patient aged 14-17 years old
  • Any gender
  • Spontaneous pneumothorax without apparent cause, between 14 and 20 years old
  • Patient operated on at the HUS between 2010 and 2021
  • Patient not objecting to the reuse of their data for scientific research purposes.
  • Holders of parental authority who do not object to the reuse of their child's data for scientific research purposes.

Exclusion criteria:

  • Patient who has expressed his opposition to the reuse of his data for scientific research purposes.
  • Holders of parental authority who have expressed their opposition to the reuse of their child's data for scientific research purposes.
  • Secondary origin of the pathology: Cystic fibrosis, postoperative pneumothorax, post-traumatic,
  • Subject having been treated initially in another structure without further information.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Retrospective description of the management of spontaneous pneumothorax in adolescents in the Strasbourg University Hospital
Time Frame: Files analysed retrospectively from January 1, 2010 and December 31, 2021 will be examined
This study is retrospective, the analysis focuses on the medical records of patients treated at the Strasbourg University Hospital between between January 1, 2010 and December 31, 2021.
Files analysed retrospectively from January 1, 2010 and December 31, 2021 will be examined

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

September 1, 2022

Primary Completion (Estimated)

December 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

September 13, 2022

First Submitted That Met QC Criteria

December 15, 2023

First Posted (Estimated)

December 18, 2023

Study Record Updates

Last Update Posted (Estimated)

December 18, 2023

Last Update Submitted That Met QC Criteria

December 15, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 8700

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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