Status:
UNKNOWN
Postoperative Opioid-Sparing Effect of a Pecto-Intercostal Fascial Block and Opioid-Free Anesthesia.
Lead Sponsor:
Algemeen Stedelijk Ziekenhuis
Conditions:
Opioid Free Anaesthesia
Opioid Anaesthesia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The present study aims to assess the difference in postoperative opioid consumption between patients who intraoperatively receive a pecto-intercostal facial block combined with opioid-free anesthesia ...
Detailed Description
Patients, aged 18 years or older, scheduled for coronary artery bypass graft surgery (CABG) with a complete midline sternotomy as surgical approach will be recruited for this study. Patients planned ...
Eligibility Criteria
Inclusion
- Aged 18 years or older
- Patients scheduled for coronary artery bypass graft surgery (CABG), which includes a complete midline sternotomy.
Exclusion
- CABG surgery which did not include a complete midline sternotomy
- Valve surgery
- Aortic surgery
- Emergency cardiac surgery
- Known allergy for ropivacaine
- Participation in another clinical trial
- Known drug abuse
- Preoperative cognitive dysfunction
- Preoperative pain therapy with opioids or anticonvulsants 14 days before surgery
- Patients unable to use Patient Controlled Analgesia (PCA)
- Need of reintubation after initial extubation
Key Trial Info
Start Date :
May 1 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2022
Estimated Enrollment :
64 Patients enrolled
Trial Details
Trial ID
NCT04854577
Start Date
May 1 2021
End Date
September 1 2022
Last Update
April 22 2021
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