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Clinical Trials/NL-OMON21054
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

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
ZonMw, Maxima MC

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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