Thorax Traumas Clinical Trial
— TraumaThoraxOfficial title:
Evaluation of Patient Analgesia After Bloc Serratus for the Management of Thoracic Trauma
| NCT number | NCT04123977 |
| Other study ID # | 7406 |
| Secondary ID | |
| Status | Recruiting |
| Phase | |
| First received | |
| Last updated | |
| Start date | October 1, 2019 |
| Est. completion date | October 2020 |
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.
| Status | Recruiting |
| Enrollment | 100 |
| Est. completion date | October 2020 |
| Est. primary completion date | October 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| France | Service de Réanimation chirurgicale_ Hôpital de Hautepierre | Strasbourg |
| Lead Sponsor | Collaborator |
|---|---|
| University Hospital, Strasbourg, France |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Retrospective analysis of analgesia after Bloc serratus | Files analysed retrospectily from January 1st, 2018 to February 28, 2019 will be examined |