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Clinical Trials in the EU / 2025-523349-86-00
Authorised Phase III

MAMI Use of the Methoxyflurane as pain-killer in the prehospital management of Acute Myocardial Infarction

2025-523349-86-00 · tracked via the Priya Life Science EU tracker
Sponsor
Assistance Publique Hopitaux De Paris
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Cardiovascular Diseases
Decision date
02/02/2026
Enrollment target
700
Sites
France

Condition studied

Acute Myocardial Infarction

Investigational medicinal product(s)

PENTHROX 999%liquide pour inhalation par vapeur de 3 mLMORPHINE

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male

Primary endpoint

Proportion of patients achieving pain relief, i.e. pain intensity score on visual analogic scale (VAS) ≤ 3 at 30 minutes.

Endpoint detail

Pain relief: time before achieving pain relief, i.e. time between randomization and pain intensity score on VAS ≤ 3;, Pain relief: time to reach initial pain divided by two (initial VAS / 2), Impact of the treatments on cardiovascular system: heart rate, arterial blood pressure, pulse oximetry and ECG changes at hospital arrival, Tolerance of the treatments: respiratory depression: respiratory rate < 10 cycles per minutes, Tolerance of the treatments: sedation: Richmond Agitation - Sedation Scale (RASS) ≥ 2 or ≤ -2, Tolerance of the treatments: : dizziness, pruritus, nausea, vomiting, headache

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-523349-86-00 on CTIS ↗ ← All trials in the EU