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.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Comparison of Low Pre-Emptive Oral Doses of Celecoxib Versus Acetaminophen for Postoperative Pain Management After Third Molar Surgery: A Randomized Controlled Study
    Xie, Long
    Yang, Rong-Tao
    Lv, Kun
    Zhou, Hai-Hua
    Li, Zhi
    JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2020, 78 (01) : 75.e1 - 75.e6
  • [42] Transmuscular quadratus lumborum block versus thoracic paravertebral block for acute pain and quality of recovery after laparoscopic renal surgery: study protocol for a randomized controlled trial
    Yuan, Qing
    Cui, Xulei
    Fei, Yuda
    Xu, Zhonghuang
    Huang, Yuguang
    TRIALS, 2019, 20 (1)
  • [43] Transmuscular quadratus lumborum block versus thoracic paravertebral block for acute pain and quality of recovery after laparoscopic renal surgery: study protocol for a randomized controlled trial
    Qing Yuan
    Xulei Cui
    Yuda Fei
    Zhonghuang Xu
    Yuguang Huang
    Trials, 20
  • [44] Efficacy of orally administered prednisolone versus partial endodontic treatment on pain reduction in emergency care of acute irreversible pulpitis of mandibular molars: study protocol for a randomized controlled trial
    Kerouredan, Olivia
    Jallon, Leonard
    Perez, Paul
    Germain, Christine
    Peli, Jean-Francois
    Oriez, Dominique
    Fricain, Jean-Christophe
    Arrive, Elise
    Devillard, Raphael
    TRIALS, 2017, 18
  • [45] Efficacy of orally administered prednisolone versus partial endodontic treatment on pain reduction in emergency care of acute irreversible pulpitis of mandibular molars: study protocol for a randomized controlled trial
    Olivia Kérourédan
    Léonard Jallon
    Paul Perez
    Christine Germain
    Jean-François Péli
    Dominique Oriez
    Jean-Christophe Fricain
    Elise Arrivé
    Raphaël Devillard
    Trials, 18
  • [46] The SWiFT trial (Study of Whole Blood in Frontline Trauma)-the clinical and cost effectiveness of pre-hospital whole blood versus standard care in patients with life-threatening traumatic haemorrhage: study protocol for a multi-centre randomised controlled trial
    Smith, Jason E.
    Barnard, Ed B. G.
    Brown-O'Sullivan, Charlie
    Cardigan, Rebecca
    Davies, Jane
    Hawton, Annie
    Laing, Emma
    Lucas, Joanne
    Lyon, Richard
    Perkins, Gavin D.
    Smith, Laura
    Stanworth, Simon J.
    Weaver, Anne
    Woolley, Tom
    Green, Laura
    TRIALS, 2023, 24 (01)
  • [47] The SWiFT trial (Study of Whole Blood in Frontline Trauma)—the clinical and cost effectiveness of pre-hospital whole blood versus standard care in patients with life-threatening traumatic haemorrhage: study protocol for a multi-centre randomised controlled trial
    Jason E. Smith
    Ed B. G. Barnard
    Charlie Brown-O’Sullivan
    Rebecca Cardigan
    Jane Davies
    Annie Hawton
    Emma Laing
    Joanne Lucas
    Richard Lyon
    Gavin D. Perkins
    Laura Smith
    Simon J. Stanworth
    Anne Weaver
    Tom Woolley
    Laura Green
    Trials, 24
  • [48] Influence of volatile anesthesia versus total intravenous anesthesia on chronic postsurgical pain after cardiac surgery using the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials criteria: study protocol for a prospective randomized controlled trial
    Yu, Hong
    Zheng, Jian-Qiao
    Hua, Yu-Si
    Ren, Shuo-Fang
    Yu, Hai
    TRIALS, 2019, 20 (01)
  • [49] Influence of volatile anesthesia versus total intravenous anesthesia on chronic postsurgical pain after cardiac surgery using the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials criteria: study protocol for a prospective randomized controlled trial
    Hong Yu
    Jian-Qiao Zheng
    Yu-Si Hua
    Shuo-Fang Ren
    Hai Yu
    Trials, 20
  • [50] Comparison of patient-controlled intravenous analgesia with sufentanil versus tramadol in post-cesarean section pain management and lactation after general anesthesia - a prospective, randomized, double-blind, controlled study
    Chi, Xiaohui
    Li, Man
    Mei, Wei
    Liao, Mingfeng
    JOURNAL OF PAIN RESEARCH, 2017, 10 : 1521 - 1527