PABLOS 2.0 - Chronic Pain After Sternotomy
- Conditions
- Anesthesia
- Registration Number
- NCT06534775
- Lead Sponsor
- University Hospital, Angers
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 253
Inclusion Criteria:<br><br> - Patient who participated in the PABLOS study (See below);<br><br> - French-speaking patient, able to understand and answer a questionnary<br><br>Exclusion Criteria:<br><br> - Patient who has had an operation for cardiac or thoracic surgery, including a REDUX<br> (surgical revision) of sternotomy since their inclusion in the PABLOS study;<br><br> - Patient opposing the research.<br><br>PABLOS criteria (NCT05345639) :<br><br>Pre-inclusion criteria<br><br> - Adult patient (=18 years old);<br><br> - Patient having planned cardiac surgery with performance of a sternotomy at the<br> Angers University Hospital;<br><br> - Patient having signed consent;<br><br> - French-speaking patient, able to understand and answer a questionnary;<br><br> - Patient affiliated to or beneficiary of a social security scheme;<br><br>Criteria for confirming inclusion<br><br> - Hemodynamic stability at the end of surgical intervention;<br><br> - Absence of bleeding justifying immediate surgical revision<br><br>Non-inclusion criteria<br><br> - Known hypersensitivity to local anesthetics with amide bonds;<br><br> - Operation for cardiac surgical revision, including REDUX (surgical revision) of<br> sternotomy;<br><br> - Emergency surgery;<br><br> - Surgery in a septic context (Endocarditis, Intravascular device infection);<br><br> - Weight less than 30kg;<br><br> - Severe psychiatric or cognitive disorder hindering assessment by questionnary;<br><br> - Pregnant, breastfeeding or parturient woman;<br><br> - Person deprived of liberty by judicial or administrative decision;<br><br> - Person subject to psychiatric care under duress;<br><br> - Person subject to a legal protection measure;<br><br> - Inclusion in another interventional study modifying post-operative pain management.
Not provided
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effectiveness of LRA
- Secondary Outcome Measures
Name Time Method LRA Impact on the intensity of exercise pain;LRA Impact on the prevalence of neuropathic pain;LRA Impact on daily consumption of analgesics;LRA Impact on quality of life;To describe all-cause mortality in cardiac surgery patients;Infection of the puncture point(s) event in context of LRA in the long term.;sternotomy scar revision in context of LRA in the long term.