跳至主要内容
临床试验/NCT00756873
NCT00756873Unknown3 期

Analgesic Efficacy and Safety of Etoricoxib in Ear Nose Throat Surgery

University of Regensburg2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2008年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
90
试验地点
2
主要终点
Post-operative opioid-sparing effect of etoricoxib in humans undergoing elective tonsillectomy

研究概览

简要总结

The aim of this study is to test the analgesic efficacy of etoricoxib (90 mg or 120 mg qd. perioperatively) for post-operative pain relief.

The primary endpoint is as follows:

  • does preoperative etoricoxib reduce the post-operative opioid utilization in patients undergoing elective tonsillectomy under general anaesthesia (i.e. the post-operative opioid-sparing effect of etoricoxib in humans).

The secondary endpoints are as follows:

  • does the etoricoxib medication have an impact on PONV or activities of daily
  • does the etoricoxib medication influence the blood loss during surgery or the incidence of postoperative bleeding
  • does the etoricoxib medication influence the operation time. In addition, adverse effects of etoricoxib will be documented.

详细描述

On day of surgery (day 0) the patients will be randomly assigned to one of the three groups using a sealed envelope method. The etoricoxib 90 mg group receives etoricoxib (Arcoxia®, Merck Sharp & Dohme GmbH, Haar, Germany) 90 mg orally, the etoricoxib 120 mg group receives etoricoxib 120 mg orally and the control group receives a placebo tablet orally 1 h before surgery (day 0). All patients receive a standard general anesthesia with intravenous propofol (2-3 mg/kg), fentanyl (2 µg/kg) and mivacurium (0.2 mg/kg) for induction. Patients are ventilated via a tracheal tube, anesthesia being maintained with sevoflurane (0.8 - 1.5% end-tidal concentration). If mean arterial blood pressure or heart rate increase to more than 25% above the pre-operative baseline value despite an end-tidal concentration of 1.5% sevoflurane, an intravenous bolus of fentanyl 0.05 mg will be administered. Monitoring includes electrocardiogram (ECG), non-invasive arterial blood pressure, pulse oximetry, end-tidal CO2 and end-tidal sevoflurane. On days 1 to 3 patients will receive etoricoxib (90 mg or 120 mg qd.) or placebo. After discharge on day 3, patients will receive etoricoxib (90 mg or 120 mg qd.) or placebo until cessation of pain during activity (swallowing). According to the current label for Arcoxia® 120 mg in Germany, patients taking etoricoxib 120 mg will switch to etoricoxib 90 mg on day 8. Rescue medication will be piritramid i.v. (day 0), oxycodone p.o. (day 1-2) and paracetamol p.o. (day 3-14).

Day -7 to -1: Inclusion/exclusion criteria, medical history, concomitant medications, laboratory, serum pregnancy test, informed consent Day 0: Study medication 1 h before surgery, intra-operative blood loss, pain score, opioid utilization, PONV score and anti-emetic medication Day 1: pain score, opioid utilization, PONV score, anti-emetic medication, bleeding Day 2: pain score, opioid utilization, PONV score, anti-emetic medication, bleeding Day 3: pain score, opioid utilization, PONV score, anti-emetic medication, bleeding Day 7: pain score, paracetamol utilization, bleeding Day 14: first day with no pain, last study medication, paracetamol utilization, bleeding

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
Triple (Participant, Care Provider, Investigator)

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

  • male or female patients
  • 18 years of age
  • female patients not pregnant/non-lactating
  • indication for elective tonsillectomy
  • written informed consent.

排除标准

  • etoricoxib, other analgesic or anti-emetic medication within 10 half-lives
  • evidence for active peptic ulceration
  • history of gastrointestinal bleeding
  • evidence of hepatic, renal or hematopoietic disorders
  • heart failure (NYHA II-IV)
  • uncontrolled arterial hypertension
  • clinical evidence of arterial occlusive disease
  • coronary heart disease or cerebrovascular disease
  • inflammatory bowel disease
  • hypersensitivity to analgetics, antipyretics, NSAIDs or antiemetics
  • evidence for noncompliance

研究组 & 干预措施

1

Placebo Comparator

干预措施: Administration of placebo (Drug)

2

Experimental

Etoricoxib 90 mg qd.

干预措施: Administration of etoricoxib (Drug)

3

Experimental

Etoricoxib 120 mg qd. (day 0-7) Etoricoxib 90 mg qd. (day 8-14)

干预措施: Administration of etoricoxib (Drug)

结局指标

主要结局

Post-operative opioid-sparing effect of etoricoxib in humans undergoing elective tonsillectomy

时间窗: Day 0-3 after surgery

次要结局

  • Impact of etoricoxib medication on PONV or activities of daily or the incidence of postoperative bleeding(Day 0-14)

研究者

申办方类型
Other

研究点 (2)

Loading locations...

相似试验