Study Type
Interventional - Procedure
The PAIN-STOP pilot study assessed the feasibility of a larger randomized controlled trial evaluating NMDA antagonists and IV steroids, as compared to placebo, in decreasing the chances of clinically significant persistent post-surgical pain (PPSP) after video assisted thoracoscopic surgeries (VATS).
Patients were recruited at two centres over five months, and followed for three months post-surgery.
Primary endpoint:
The proportion of:
1) eligible patients recruited;
2) patients adhering to the study protocol; and
3) patients completing the follow-up at three months.
Along with PHRI’s PJ Devereaux, the co-Principal Investigator of the PAIN-STOP study was Harsha Shanthanna, Associate Professor, Anesthesia, McMaster University.
Interventional - Procedure
Multi-centre, blinded, randomized controlled trial with 2 X 2 factorial design
1
1
48
2017
PHRI
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