跳至主要内容
临床试验/NCT03640247
NCT03640247已完成1 期

Are Narcotic Pain Medications Necessary Following Thyroidectomy and Parathyroidectomy

MetroHealth Medical Center1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2018年11月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
126
试验地点
1
主要终点
Overall mean pain as assessed by 10 point visual analogue scale from the 6 post operative day time points.

研究概览

简要总结

The purpose of this study is to evaluate the use of a non-narcotic, postoperative pain management regimen on patients undergoing thyroidectomy and parathyroidectomy.

详细描述

The purpose of this study is to evaluate the use of a non-narcotic, postoperative pain management regimen for patients undergoing thyroidectomy and parathyroidectomy. The investigators hypothesize that participants receiving non-narcotic pain regimens will have equivalent pain control and satisfaction to those who receive narcotic pain medicines.

The primary objective will be to identify if there is a difference in average perceived postoperative pain scores between participants who do and do not receive narcotic pain medications. Secondary outcomes will include need for breakthrough pain medications, patient satisfaction scores and the need to call the surgeon office for additional pain medications.

The participant will undergo total thyroidectomy, partial thyroidectomy or parathyroidectomy per the standard of care. The study will have no influence on the surgical procedure performed.

Following the surgery, postoperative analgesia regimens will be prescribed based on study randomization.

Narcotic group regimen (63 patients):

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
None

盲法说明

All party or parties involved have knowledge of the interventions assigned to individual participants

入排标准

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

入选标准

  • Age 18 years or greater
  • Undergoing total thyroidectomy, partial thyroidectomy or parathyroidectomy at MetroHealth Medical Center

排除标准

  • Patients taking narcotics prior to surgery
  • Patients who are unable or unwilling to follow study protocol requirements

研究组 & 干预措施

Narcotic group regimen

Other
  • Tylenol tablet 1000 mg by mouth every 8 hours alternating with
  • Ibuprofen tablet 800 mg by mouth every 8 hours
  • Oxycodone 5 mg by mouth every 6 hours as needed for pain, #10 tablet or if needed based on patient allergies, hydrocodone 5 mg/tramadol 50 mg.

干预措施: Narcotic group regimen (Drug)

Non-narcotic group regimen

Active Comparator
  • Tylenol tablet 1000 mg by mouth every 8 hours alternating with
  • Ibuprofen tablet 800 mg by mouth every 8 hours

干预措施: Non-narcotic group regimen (Drug)

结局指标

主要结局

Overall mean pain as assessed by 10 point visual analogue scale from the 6 post operative day time points.

时间窗: Overall mean pain score from 6 time points (Post operative days 0,1,2,3,4,5)

10 point visual analogue scale- (0- no pain, 1-3 mild, 4-6 moderate pain, 7-10 severe pain).

次要结局

  • Patient satisfaction with the pain medication regimen as assessed by 3-point likert scale from the 6 post operative day time points.(Mean patient satisfaction score from 6 time points (Post operative days 0,1,2,3,4,5))
  • Total dose of oral narcotics converted into oral morphine equivalents (see below) that were taken by participants post-operatively(Mean oral morphine equivalents from 6 time points (Post operative days 0,1,2,3,4,5))
  • Mean number of office calls/contacts from the 6 post operative day time points.(Mean number of office calls/contacts from 6 time points (Post operative days 0,1,2,3,4,5))

研究者

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

Christopher McHenry

MD, Director, Division of General Surgery

MetroHealth Medical Center

研究点 (1)

Loading locations...

相似试验