Pleuropulmonary Echography Versus Standard Chest X-ray in the Post-operative Follow-up of Pleuropulmonary Surgery
NCT ID: NCT03835130
Last Updated: 2019-08-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
40 participants
OBSERVATIONAL
2019-01-25
2019-07-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This repeated performance of radiographs results in irradiation of patients but also of medical staff and a significant cost.
In the thoracic study, ultrasound imaging is a fast, cost-effective, non-irradiating solution that can be performed at the patient's bedside. It could guide the performance of chest x-ray, limit their number, with increased clinical relevance.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Management of Parapneumonic Pleurisy Guided by an Early Pleural Ultrasound
NCT04348734
Nurse-performed Lung Ultrasound Versus Chest Radiography for Detection of Pneumothorax.
NCT04678726
Comparison Of Chest Ultrasound Techniques To Identify Clinically Significant Pneumothorax
NCT02619591
Lung Ultrasound for the Postoperative Diagnosis of Pneumothorax in Children
NCT03073616
The Added Value of CT Scanning in Patients With an Unilateral Pleural Effusion
NCT03270215
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
OTHER
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Hospitalized patient at Martinique University Hospital
* Patient receiving social security
* Patient giving his free and informed consent orally
Exclusion Criteria
* Woman who is pregnant and breast feeding
* Patient no giving his free and informed consent orally
18 Months
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital Center of Martinique
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nicolas VENISSAC, MD-PhD
Role: PRINCIPAL_INVESTIGATOR
CHU de Martinique
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU Martinique
Fort-de-France, , Martinique
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
18_RIPH3-06
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.