Evidence map›Paper›PMID 34880961›Full record

Trial reportPain research & management

Pharmacokinetic Characterisation and Comparison of Bioavailability of Intranasal Fentanyl, Transmucosal, and Intravenous Administration through a Three-Way Crossover Study in 24 Healthy Volunteers.

S Nardi-Hiebl, J W Ndieyira, Y Al Enzi, W Al Akkad, T Koch, G Geldner, C Reyher, L H J Eberhart

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Pain research & management. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 3 countries.

S Nardi-HieblDepartment of Anaesthesia and Intensive Care, University Hospital Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0003-3563-3505
J W NdieyiraDivision of Medicine, University College London, London, UK.ORCID https://orcid.org/0000-0002-3466-7327
Y Al EnziDepartment of Mathematics and Natural Science, Gulf University of Science and Technology, Mubarak Al-Abdullah, Kuwait.
W Al AkkadRoyal Free London Hospital, University College London, London, UK.ORCID https://orcid.org/0000-0002-0109-3021
T KochDepartment of Anaesthesia and Intensive Care, University Hospital Marburg, Marburg, Germany.
G GeldnerDepartment of Anaesthesiology Intensive Care Medicine Emergency Medicine and Pain Therapy, RKH Kliniken-Hospital Ludwigsburg, Ludwigsburg, Germany.
C ReyherDepartment of Anaesthesiology Intensive Care Medicine Emergency Medicine and Pain Therapy, Klinikum Kassel GmbH, Kassel, Germany.
L H J EberhartDepartment of Anaesthesia and Intensive Care, University Hospital Marburg, Marburg, Germany.
Philipps University of Marburg · DEGulf University for Science & Technology · KWKlinikum Kassel · DEKlinikum Ludwigsburg · DEThe Royal Free Hospital · GBUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor more than 60 years, the synthetic opioid fentanyl has been widely used in anaesthesia and analgesia. While the intravenous formulation is primarily used for general anaesthesia and intensive care settings, the drug's high lipophilic properties also allow various noninvasive routes of administration. Published data suggest that intranasal administration is also attractive for use as intranasal patient-controlled analgesia (PCA). A newly developed intranasal fentanyl formulation containing 47

methods27 healthy volunteers were enrolled in a single-centre, open-label, randomised (order of treatments), single-dose study in a three-period crossover design. The pharmacokinetics of one intranasal puff of fentanyl formulation (47

results24 volunteers completed the study. The geometric mean of AUC

conclusionPharmacokinetic parameters and bioavailability of the investigated intranasal fentanyl indicated suitability for its intended use as an intranasal PCA option.

Indexed as

FentanylTandem Mass SpectrometryAdministration, IntranasalAdministration, IntravenousAdministration, MucosalAdministration, OralArea Under CurveBiological AvailabilityCross-Over StudiesHealthy VolunteersHumansInfusions, IntravenousFentanyl

Identifiers

PMID34880961
PMCPMC8648480
OpenAlexW3215019598

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.