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).
Randi SimensenLars Olav FjoseMarius RehnJostein HagemoKjetil ThorsenFridtjof HeyerdahlPublished in: Trials (2023)
We 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. PreMeFen 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.
Keyphrases
- pain management
- chronic pain
- neuropathic pain
- randomized controlled trial
- cardiac arrest
- liver failure
- healthcare
- respiratory failure
- newly diagnosed
- anti inflammatory
- ejection fraction
- emergency department
- adverse drug
- study protocol
- high dose
- clinical trial
- low dose
- acute care
- mechanical ventilation
- electronic health record