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CompletedNCT01975753AEROMORPH1Updated Oct 24, 2019

First Evaluation of Morphine Hydrochloride by Nebulisation in Healthy Volunteers

A Phase 1/2 interventional study of Morphine and Fentanyl in Acute Pain, sponsored by University Hospital, Rouen. Completed at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-10-24.

Sponsored by University Hospital, Rouen · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
35
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Acute pain relief in emergency setting is still a public health priority. Pain is the primary reason for emergency room use, but the situation of "oligo-analgesia" persists in all countries. Intravenous morphine titration has become the standard method for severe acute pain management in the emergency department, but it is still insufficiently implemented. Deviations from the recommended protocol are common: initial additional loading doses, unusually extended intervals between bolus, premature discontinuation. Several factors contribute to these difficulties: heaviness of its setting up, especially in overcrowding case, procedure rigidity, high consumption of nursing time. This method requires a systematic intravenously route, which has several inconvenients: algogenic procedures, coupled initial diagnostic venous sampling (delay for analgesia), excessive "medicalization" of ambulatory patients (risk of infection and less mobility in the emergency department). An alternative to reduce the analgesic latency in emergency department, without losing the benefits of tolerance and safety should be welcome. The inhaled route looks promising, but has yet not been enough evaluated in adults, and even less in the emergency room. Aerosol techniques change from one study to another (molecules, materials, doses, painful intensities included, judgment criteria and assessment times). A morphine titration by aerosol therapy could be an interesting alternative to the standard method disadvantages, using faster, painless and easier procedures, leading to "demedicalization".

To the need for stronger fundamentals, an additional study was designed in healthy volunteers. The objective is to compare the titration of intravenous morphine titration aerosol in moderate acute pain caused by electrostimulation.

To purchase this aim, we first need to determine accurately the smallest dose of effective and well tolerated inhaled morphine, to provide the "bolus" dose we have to repeat by titration, which is still currently unknown. This dose is called ED50, it's the effective dose for at least 50% of healthy volunteers relieved. ED50 for intravenous morphine is also needed to be established, unknown in this indication. The determination of these two parallel ED50 would allow a reliable conversion factor between the two routes of administration for morphine "bolus", which can then be tested in comparative titrations. To validate our induced pain model in healthy volunteers, we also have chosen to fix in these conditions the ED50 of fentanyl that the effective dose by nebulization is better known. This study would also describe the pharmacokinetics of inhaled morphine and its derivatives after a single spray.

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Conditions studied

  • Acute Pain

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Keywords

  • pain
03

In context

Acute Pain

908 studies on the registry are indexed under Acute Pain; 154 are open to participants now.

This study's enrollment of 35 is below the median of 87 across 759 interventional studies indexed under Acute Pain.

Browse Acute Pain studies →

Lead sponsor

University Hospital, Rouen is the lead sponsor of 416 studies on the registry; 105 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Sex: We choose to include 50% of men and 50% women (this covariate will be included in the parameters to balance the randomization list).
  • Age: Healthy volunteers will be between 18 to 60 years
  • Body mass index (BMI) between 19 and 29 kg / m²
  • effective contraception methods in women of childbearing age
  • Signature of informed consent
  • Affiliation to a social security scheme

Exclusion criteria

Exclusion Criteria:

  • Taking painkillers long-term
  • Taking psychotropic drugs long-term
  • Healthy volunteers with chronic pain
  • Drug addiction
  • Chronic neuropsychiatric pathology which may alter the pain threshold
  • Active Smoking
  • Chronic obstructive or restrictive respiratory pathology
  • Progressive known pathology (hypertension, kidney failure, heart, liver ...)
  • Chronic treatments are prohibited except oral contraception
  • Delirium or dementia, people who did not understand the pain scales
  • Lack of understanding of the French language
  • pregnancy and lactation
  • Poor venous capital
  • History of abnormal reaction at a local / regional anesthesia
  • Heart rate : HR \<50 bpm
  • Hypotension TAsyst with systolic blood pressure \<100 mm Hg
  • Atrioventricular block (PR interval> 200 ms)
  • Period exclusion of another biomedical research
  • Nobody placed under judicial protection, guardianship
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Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
35 participants (actual)

Study arms

  • Active comparator
    Intravenous morphine

    one bolus of intravenous morphine

    Drug: Morphine

  • Experimental
    nebulized morphine

    one "nebulized" bolus of morphine

    Drug: Morphine

  • Active comparator
    fentanyl

    one "nebulized" bolus of fentanyl

    Drug: Fentanyl

Interventions

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What researchers measure

Primary outcomes

  1. Effective doses of intravenous morphine hydrochloride "bolus" and nebulized "bolus" in 50% of healthy painful volunteers

    The primary endpoint is efficacy: relief from healthy volunteers thanks to VAS decreasing, defined as ≤ 20 (100mm). At the end of the study the dose chosen is the effective dose for 50% of the volunteers.

    Time frame: 7 min

Secondary outcomes

  1. safety

    Check tolerance of aerosols on respiratory and systemically 2. Describe the pharmacokinetics of a "bolus" and a titration of morphine hydrochloride aerosol standardized, and of all its metabolites 3. Establish the concentration-effect relationship of a spray "bolus" and of a titration of morphine hydrochloride standardized (for the analgesic effect) using a pharmacokinetic / pharmacodynamic model (PK / PD) and mathematical modeling 4. Methodological validation by determining the ED50 of a inhaled fentanyl "bolus" 5. Establish pharmacokinetic bases that can provide a secure further study in the emergency room, targeting patients with severe spontaneous acute pain

    Time frame: 7 min

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Study locations

1 site
  • University Hospital
    Rouen, Haute Normandie 76000, France
08

References and documents

Publications

  • Lvovschi V, Aubrun F, Bonnet P, Bouchara A, Bendahou M, Humbert B, Hausfater P, Riou B. Intravenous morphine titration to treat severe pain in the ED. Am J Emerg Med. 2008 Jul;26(6):676-82. doi: 10.1016/j.ajem.2007.10.025. PubMed 18606320 ↗
  • Blum CA, Velly L, Brochet C, Ziegler F, Tavolacci MP, Hausfater P, Lvovschi VE. Relevance of cortisol and copeptin blood concentration changes in an experimental pain model. Sci Rep. 2022 Mar 19;12(1):4767. doi: 10.1038/s41598-022-08657-4. PubMed 35306524 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 24, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01975753
Responsible party
Sponsor
First posted
Nov 5, 2013
Start date
May 13, 2014
Primary completion
May 2, 2018
Completion
May 2, 2018
Last update
Oct 24, 2019

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Morphine

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