Evidence map›Paper›PMID 31094746›Full record

Trial reportAnesthesiology2019

Dextromethorphan Analgesia in a Human Experimental Model of Hyperalgesia.

E Martin, C Narjoz, X Decleves, L Labat, C Lambert, M-A Loriot, G Ducheix, C Dualé, B Pereira, G Pickering

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Anesthesiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02596360 (Dextromethorphan Effect on Central Sensitization to Pain in Healthy Volunteers), which is not on this map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 23% 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.

NCT02596360 phase1completednot on this map

Dextromethorphan Effect on Central Sensitization to Pain in Healthy Volunteers

TypeinterventionalSponsorUniversity Hospital, Clermont-FerrandRan2015 to 2016Enrolled20ConditionsExperimental Pain, HyperalgesiaArmsPulmodexane® 30mg, lactose
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 4 countries.

E MartinFrom University Clermont Auvergne, Department of Fundamental and Clinical Pharmacology of Pain, NeuroDol, F-63000 Clermont-Ferrand, France (E.M., C.D., G.P.) Inserm UMR-S1147, Saints-Pères University Centre, Paris, France (C.N., M.-A.L.) University Paris Descartes, Sorbonne Paris Cité, Paris, France (C.N., M.-A.L.) Assistance Publique-Paris Hospital (AP-HP), Georges Pompidou European Hospital, Biochemistry Department, Paris, France (C.N., M.-A.L.) Cochin Hospital, HUPC, Hôpitaux de Paris (AP-HP) Paris, France (X.D., L.L.) Pharmacy Faculty, University Paris Descartes Inserm UMR-S1144, Paris, France (X.D.) Clermont-Ferrand, Research and Innovation Department, Clermont-Ferrand, France (C.L., B.P.) University Hospital Clermont-Ferrand, Clinical Pharmacology Department/Clinical Research Centre, Inserm 1405, F-63003 Clermont-Ferrand, France (G.D., C.D., G.P).
C Narjoz
X Decleves
L Labat
C Lambert
M-A Loriot
G Ducheix
C Dualé
B Pereira
G Pickering
Délégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCentral pain sensitization is often refractory to drug treatment. Dextromethorphan, an N-methyl-D-aspartate receptor antagonist, is antihyperalgesic in preclinical pain models. The hypothesis is that dextromethorphan is also antihyperalgesic in humans.

methodsThis randomized, double-blind, placebo-controlled, crossover study explores the antihyperalgesic effect of single and repeated 30-mg dose of oral dextromethorphan in 20 volunteers, using the freeze-injury pain model. This model leads to development of primary and secondary hyperalgesia, which develops away from the site of injury and is associated with central sensitization and activation of N-methyl-D-aspartate receptor in the spinal cord. The primary outcome was antihyperalgesia calculated with the area under the curve of the percentage change in mechanical pain threshold (electronic von Frey) on the area of secondary hyperalgesia. The secondary outcomes were mechanical pain threshold on the area of primary hyperalgesia and cognitive (reaction time) effect.

resultsSingle 30-mg results are reported. Antihyperalgesia (% · min) is significantly higher on the area of secondary hyperalgesia with dextromethorphan than placebo (median [interquartile range]: 3,029 [746; 6,195] vs. 710 [-3,248; 4,439], P = 0.009, Hedge's g = 0.8, 95% CI [0.1; 1.4]). On primary hyperalgesia area, mechanical pain threshold 2 h after drug intake is significantly higher with dextromethorphan (P = 0.011, Hedge's g = 0.63, 95% CI [0.01; 1.25]). No difference in antinociception is observed after thermal painful stimuli on healthy skin between groups. Reaction time (ms) is shorter with placebo than with dextromethorphan (median [interquartile range]: 21.6 [-37.4; 0.1] vs. -1.2 [-24.3; 15.4], P = 0.015, Hedge's g = 0.75, 95% CI [0.12; 1.39]). Nonserious adverse events occurrence (15%, 3 of 20 volunteers) was similar in both groups.

conclusionsThis study shows that low-dose (30-mg) dextromethorphan is antihyperalgesic in humans on the areas of primary and secondary hyperalgesia and reverses peripheral and central neuronal sensitization. Because dextromethorphan had no intrinsic antinociceptive effect in acute pain on healthy skin, N-methyl-D-aspartate receptor may need to be sensitized by pain for dextromethorphan to be effective.

Indexed as

AnalgesiaCross-Over StudiesDextromethorphanDouble-Blind MethodExcitatory Amino Acid AntagonistsHumansHyperalgesiaMaleNeuralgiaTreatment OutcomeDextromethorphanExcitatory Amino Acid Antagonists

Identifiers

PMID31094746
OpenAlexW2945345820

What OpenQuestion holds

Textmetadata
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.