The effect of rate of administration of tramadol on incidence of post operative nausea and vomiting after any surgical operation for which significant postoperative pain is expected

Category Primary study
Registry of TrialsANZCTR
Year 2006
INTERVENTION: ‘Fast’ group – will receive 2.5 mg/kg tramadol (made to 10 ml with addition of saline) intravenously over 2 minutes and 10 ml saline via a syringe driver over 30 minutes. ‘Slow’ group – will receive 10 ml saline over 2 minutes and 2.5 mg/kg tramadol (made to 10 ml with addition of saline) intravenously via a syringe driver over 30 minutes. CONDITION: Post operative nausea and vomiting PRIMARY OUTCOME: Comparative peak change from baseline in nausea visual analogue score (VAS) scores between fast, slow and placebo tramadol administration groups SECONDARY OUTCOME: Comparative vomiting frequencies, morphine PCA usage, pain scores, duration spent in PACU and patient satisfaction scores between fast, slow and placebo tramadol administration groups over three hours. INCLUSION CRITERIA: English spoken as first language, or fluent as a second language• Scheduled to have elective non‐abdominal surgery under general anaesthesia (including general, orthopaedic, plastic, ENT, urologic, dental or vascular surgery) • Requiring general anaesthesia• Significant post‐operative pain requiring opioid therapy expected.
Epistemonikos ID: af8003a4ab568ba2ccbcfd3ee2501c9d3cbf19ca
First added on: Aug 25, 2024