Comparison of three regimens with inhalational methoxyflurane versus intranasal fentanyl versus intravenous morphine in pre-hospital acute pain management: study protocol for a randomized controlled trial (PreMeFen)

被引:3
作者
Simensen, Randi [1 ,2 ,3 ,4 ]
Fjose, Lars Olav [1 ,2 ]
Rehn, Marius [2 ,3 ,4 ]
Hagemo, Jostein [2 ,3 ,4 ]
Thorsen, Kjetil [2 ]
Heyerdahl, Fridtjof [2 ,3 ,4 ]
机构
[1] Innlandet Hosp Trust, Div Prehosp Serv, Kastbakkvegen 9, N-2390 Moelv, Norway
[2] Norwegian Air Ambulance Fdn, Dept Res, Oslo, Norway
[3] Oslo Univ Hosp, Div Prehosp Serv, Oslo, Norway
[4] Univ Oslo, Inst Clin Med, Fac Med, Oslo, Norway
关键词
Analgesia; Pre-hospital; Emergency medicine; Acute pain; Opioids; Methoxyflurane; TRAUMA PAIN; ANALGESIA; INTENSITY;
D O I
10.1186/s13063-023-07590-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundPre-hospital pain management has traditionally been performed with intravenous (IV) morphine, but oligoanalgesia remain a recognized problem. Pain reduction is essential for patient satisfaction and is regarded as a measure of successful treatment. We aim to establish whether non-invasive methods such as inhalation of methoxyflurane is non-inferior to intranasal fentanyl or non-inferior to the well-known IV morphine in the pre-hospital treatment of acute pain.Method/designThe PreMeFen study is a phase three, three-armed, randomized, controlled, non-inferiority trial to compare three regimens of analgesics: inhalation of methoxyflurane and intranasal (IN) fentanyl versus IV morphine. It is an open-label trial with a 1:1:1 randomization to the three treatment groups. The primary endpoint is the change in pain numeric rating scale (NRS) (0-10) from baseline to 10 min after start of investigational medicinal product administration (IMP). The non-inferiority margin was set to 1.3, and a sample size of 270 patients per protocol (90 in each treatment arm) will detect this difference with 90% power.DiscussionWe chose a study design with comparison of analgesic regimens rather than fixed doses because of the substantial differences in drug characteristics and for the results to be relevant to inform policymakers in the pre-hospital setting. We recognize that easier administration of analgesics will lead to better pain management for many patients if the regimens are as good as the existing, and hence, we chose a non-inferiority design. The primary endpoint, the change in pain (NRS) after 10 min, is set to address the immediate need of pain reduction for patients with acute prehospital pain. On a later stage, more analgesic methods are often available.SummaryPreMeFen is a non-inferiority randomized controlled trial comparing three analgesic regimens aiming to establish whether inhalation of methoxyflurane or intranasal fentanyl is as good as IV morphine for fast reduction of acute pain in the prehospital setting.
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