Evidence map›Paper›PMID 25302017›Full record

Trial reportDrug design, development and therapy2014

Buccal acetaminophen provides fast analgesia: two randomized clinical trials in healthy volunteers.

Gisèle Pickering, Nicolas Macian, Frédéric Libert, J Michel Cardot, Séverine Coissard, Philippe Perovitch, Marc Maury, Claude Dubray

2 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Drug design, development and therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 33% 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.

NCT00982215 phase1completednot on this map

Pilot Study of Pharmacology of Paracetamol Administered Per-oral Mucosa

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2009 to 2009Enrolled20ConditionsHealthyArmsKinetics of plasma concentrations of paracetamol, Placebo
NCT01206985 phase1completednot on this map

Pharmacodynamic Study of 125 mg of Paracetamol Permucosal Administered by Sublingual and Buccal Route

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2010 to 2011Enrolled20ConditionsHealthy VolunteersArmsVon Frey electronic
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
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 1 institution in 1 country.

Gisèle PickeringCHU Clermont-Ferrand, Centre de Pharmacologie Clinique, Clermont-Ferrand, France ; Inserm, Clermont-Ferrand, France ; Clermont Université, Laboratoire de Pharmacologie, Faculté de Médecine, Clermont-Ferrand, France.
Nicolas MacianCHU Clermont-Ferrand, Centre de Pharmacologie Clinique, Clermont-Ferrand, France.
Frédéric LibertInserm, Clermont-Ferrand, France ; Laboratoire de Pharmacologie, CHU Clermont-Ferrand, France.
J Michel CardotCHU Clermont-Ferrand, Centre de Pharmacologie Clinique, Clermont-Ferrand, France.
Séverine CoissardCHU Clermont-Ferrand, Centre de Pharmacologie Clinique, Clermont-Ferrand, France.
Philippe PerovitchUnither Pharamceuticals, Paris, France.
Marc MauryUnither Pharamceuticals, Paris, France.
Claude DubrayCHU Clermont-Ferrand, Centre de Pharmacologie Clinique, Clermont-Ferrand, France ; Inserm, Clermont-Ferrand, France ; Clermont Université, Laboratoire de Pharmacologie, Faculté de Médecine, Clermont-Ferrand, France.
Centre Hospitalier Universitaire de Clermont-Ferrand · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcetaminophen (APAP) by oral or intravenous (iv) routes is used for mild to moderate pain but may take time to be effective. When fast relief is required and/or oral or iv routes are not available because of the patient's condition, the transmucosal route may be an alternative. METHODOLOGY: A new transmucosal/buccal (b) pharmaceutical form of APAP dissolved in 50% wt alcohol is compared with other routes of administration. Two consecutive randomized, crossover, double-blind clinical trials (CT1: NCT00982215 and CT2: NCT01206985) included 16 healthy volunteers. CT1 compared the pharmacology of 250 mg bAPAP with 1 g iv APAP. CT2 compared the pharmacodynamics of 125 mg bAPAP with 1 g iv and 125 mg sublingual (s) APAP. Mechanical pain thresholds are recorded in response to mechanical stimuli applied on the forearm several times during 120 minutes. The objective is to compare the time of onset of antinociception and the antinociception (area under the curve) between the routes of administration with analysis of variance (significance P<0.05).

resultsbAPAP has a faster time of antinociception onset (15 minutes, P<0.01) and greater antinociception at 50 minutes (P<0.01, CT1) and 30 minutes (P<0.01, CT2) than ivAPAP and sAPAP. All routes are similar after 50 minutes.

conclusionbAPAP has a faster antinociceptive action in healthy volunteers. This attractive alternative to other routes would be useful in situations where oral or iv routes are not available. This finding must now be confirmed in patients suffering from acute pain of mild and moderate intensity.

Indexed as

AnalgesiaAcetaminophenAdministration, BuccalAdultCross-Over StudiesDose-Response Relationship, DrugDouble-Blind MethodHealthy VolunteersHumansMalePainPain MeasurementTime FactorsAcetaminophenhealthy volunteerpaintransmucosal delivery

Identifiers

PMID25302017
PMCPMC4189711
OpenAlexW2007475852

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.