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临床试验/NCT07226076
NCT07226076招募中3 期

Reduction of Post-op Pain and Opioid Consumption With the Addition of Methadone in Total Knee Arthroplasty: a Double-blind Randomized Control Trial

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 162 人开始时间: 2026年1月8日最近更新:
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
162
试验地点
1
主要终点
Patient reported pain in the recovery unit after surgery

研究概览

简要总结

This randomized, double-blind controlled trial investigates whether intraoperative IV methadone (0.15 mg/kg based on ideal body weight) reduces acute postoperative pain and opioid consumption in patients undergoing elective total knee arthroplasty under spinal anesthesia with mepivacaine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ages 18-75 years of age
  • Undergoing elective primary total knee arthroplasty with mepivacaine in the spinal anesthesia
  • Allergy to methadone or mepivacaine
  • Severe liver disease defined as Child's Pugh Class C
  • End stage renal disease requiring dialysis
  • Known diagnosis of prolonged QT syndrome
  • Currently pregnant
  • Unable to provide written, informed consent
  • Non-English speaking

排除标准

  • 未提供

研究组 & 干预措施

Methadone

Active Comparator

Patients will intraoperatively receive methadone 0.15mg/kg IV, based on ideal body weight.

干预措施: Methadone Hydrochloride (Drug)

No Methadone

No Intervention

Patients will NOT receive methadone.

结局指标

主要结局

Patient reported pain in the recovery unit after surgery

时间窗: up to 24 hours after surgery ends

Patient reported pain on a Visual Analog Scale (VAS) from 0-100mm at approximately 30-60 minutes after arriving to the recovery unit after surgery. A lower pain score means a better outcome.

次要结局

  • Time to first opioid rescue dose(up to 24 hours after surgery ends)
  • Opioid Consumption in the recovery unit(PACU Arrival until PACU Discharge up to 30 days)
  • Pain scores(PACU, 24 hours, 48 hours, and 72 hours post-operatively.)
  • Postoperative nausea and/or vomiting(PACU through 72 hours post-operatively)
  • Quality of Recovery(up to 24-hours post-operatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

William Barrett

Assistant Professor-Faculty

Medical University of South Carolina

研究点 (1)

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