NL-OMON21054
Recruiting
Not Applicable
Optimal postoperative Pain management After Lung surgery (OPtriAL): multicenter randomised clinical trial
ZonMw, Maxima MC0 sites571 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ZonMw, Maxima MC
- Enrollment
- 571
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
/A
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients referred for anatomical lung resection (pneumonectomy, (bi)lobectomy or segmentectomy) with the intention of performing it by VATS or RATS are eligible for the trial.
- •\- Adult patients older than 18 years who are able to give informed consent and fill out questionnaires in Dutch.
Exclusion Criteria
- •\- Contra\-indications TEA or PVB (infection at skin site, increased intracranial pressure, non\-correctable coagulopathy, bridging indication for therapeutic anticoagulation (CHADS\-VASc \= 8\), sepsis and mechanical spine obstruction)
- •\- Allergy to local anaesthetics
- •\- Chronic use of opioids
- •\- In case the lung surgeon estimates the operation to be performed through a thoracotomy technique instead of a VATS the patient will be excluded.
Outcomes
Primary Outcomes
Not specified
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