- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04123977
Evaluation of Patient Analgesia After Bloc Serratus (TraumaThorax)
Evaluation of Patient Analgesia After Bloc Serratus for the Management of Thoracic Trauma
Thorax traumas are very common in severe traumatology, including road accidents, representing the second most frequent site (after head injury, according to the FIRST study). These thoracic lesions are the cause of many complications (pneumothorax, hemothorax, lung infections, atelectasis).
The national recommendations recommend the use of multi-modal analgesia with the use of regional loco anaesthesia for pain management and prevention of respiratory complications, including infectious complications. The loco-regional anaesthesia of choice is thoracic epidural or paravertebral block, but these techniques are not without risks, and are contraindicated in many situations (severe head trauma, patient under curative anticoagulation, pelvic trauma...).
The anterior Serratus block appears to be a quality localoregional anaesthesia in thoracic surgery, and a few cases in the literature have shown an interest in severe traumatology.
The investigators perform this anterior Serratus block almost systematically in patients with thoracic trauma in the Hautepierre surgical intensive care unit.
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Julien POTTECHER, MD, PhD
- Phone Number: 33 3 88 12 70 95
- Email: julien.pottecher@chru-strasbourg.fr
Study Contact Backup
- Name: Kevin COGNE, MD
- Phone Number: 33 3.88 12 61 55
- Email: kevin.cogne@chru-strasbourg.fr
Study Locations
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-
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Strasbourg, France, 67091
- Recruiting
- Service de Réanimation chirurgicale_ Hôpital de Hautepierre
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Contact:
- Julien POTTECHER, MD, PhD
- Phone Number: 33 3 88 12 70 95
- Email: julien.pottecher@chru-strasbourg.fr
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Principal Investigator:
- Julien POTTECHER, MD, PhD
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Sub-Investigator:
- Kevin COGNE, MD
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Contact:
- Kevin COGNE, MD
- Phone Number: 33 3 88 12 61 55
- Email: kevin.cogne@chru-strasbourg.fr
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Sub-Investigator:
- Paul BRUNET, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
- Adult patient (≥18 years old)
- Gender (Male and Female)
- Patient hospitalised in surgical intensive care or continuous trauma care with thorax trauma who received anterior Serratus block analgesia from January 1, 2018 to February 28, 2019
- Patient who has given his consent to the reuse of his data for the purposes of this research
Criteria for non-inclusion:
- Patient who has expressed opposition to participating in the study
- Impossibility of giving the subject informed information (difficulties in understanding the subject,...)
- Subject under the protection of justice
- Subject under guardianship or curatorship
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Retrospective analysis of analgesia after Bloc serratus
Time Frame: Files analysed retrospectily from January 1st, 2018 to February 28, 2019 will be examined
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Files analysed retrospectily from January 1st, 2018 to February 28, 2019 will be examined
|
Collaborators and Investigators
Investigators
- Study Director: Julien POTTECHER, MD, PhD, University Hospital, Strasbourg, France
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7406 (Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium)
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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