Table 1.
Study Period | |||||||
---|---|---|---|---|---|---|---|
Timepoint | Enrollment | Allocation | Post-Allocation | Closeout | |||
Preoperative Visit | Before Surgery | During Surgery | Postoperative Care Unit | Day 1 | Day 2 | Hospital Discharge | |
Enrollment | |||||||
Inclusion criteria | × | ||||||
Exclusion criteria | × | ||||||
Written informed consent | × | ||||||
Baseline data | × | ||||||
Randomization | × | ||||||
Allocation | × | ||||||
Interventions | |||||||
Intravenous lidocaine | × | × | |||||
Quadratus lumborum block | × | ||||||
Assessments | |||||||
Sufentanil consumption | × | × | |||||
Pain at rest | × | × | × | ||||
Pain on coughing | × | × | × | ||||
Rescue analgesia | × | × | × | ||||
Postoperative nausea and vomiting | × | × | × | ||||
Quality of recovery | × | × | |||||
Adverse events | × | × | |||||
Postoperative hospital stay | × |
Notes: According to SPIRIT statement of defining standard protocol items for clinical trials.