Evidence map›Paper›PMID 38783265›Full record

ArticleBMC veterinary research2024

Re-evaluating the placebo response in recent canine dietary epilepsy trials.

Teresa Schmidt, Nina Meyerhoff, Sebastian Meller, Friederike Twele, Marios Charalambous, Benjamin A Berk, Tsz H Law, Rowena M A Packer, Brian Zanghi, Yuanlong Pan and 2 more

Abstract read
In one paragraph

Article in BMC veterinary research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

12 authors.

Teresa SchmidtDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Nina MeyerhoffDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Sebastian MellerDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Friederike TweleDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Marios CharalambousDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany.
Benjamin A BerkBrainCheck.Pet® - Tierärztliche Praxis für Epilepsie, Mannheim, Germany.
Tsz H LawDepartment of Clinical Science and Services, Royal Veterinary College, Hatfield, UK.
Rowena M A PackerDepartment of Clinical Science and Services, Royal Veterinary College, Hatfield, UK.
Brian ZanghiResearch and Development, Nestlé Purina PetCare, St. Louis, MO, USA.
Yuanlong PanResearch and Development, Nestlé Purina PetCare, St. Louis, MO, USA.
Andrea FischerCentre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.
Holger A VolkDepartment of Small Animal Medicine and Surgery, University of Veterinary Medicine Hannover, Hannover, Germany. Holger.Volk@tiho-hannover.de.

Funding

American Kennel Club Canine Health Foundation 2252Biotechnology and Biological Sciences Research Council BB/P001874/1, BB/J012491/1
6 · The paper itself

Abstract

The placebo response is a common phenomenon. Limited evidence is available about its magnitude in canine epilepsy trials, even though it can significantly influence the efficacy evaluation of new treatments. It was hypothesised that the placebo response is diminished when epilepsy trials are conducted in a prospective crossover design. Seizure data spanning six months from three previous multicenter epilepsy studies were analysed. The monthly seizure frequency of 60 dogs diagnosed with idiopathic epilepsy was calculated, comparing baseline data with placebo treatment. Furthermore, differentiation was made between dogs randomised to the placebo group early (Phase 1: first 3 months) or later during the study (Phase 2: second 3 months).The analysis did not reveal any placebo response in terms of monthly seizure frequency. Instead, an increase was noted during the placebo treatment period, with a mean of 2.95 seizures per month compared to 2.30 seizures per month before study entry (p = 0.0378). Additionally, a notable phase effect was observed. Dogs receiving the placebo in the second study phase exhibited a significant increase in monthly seizure frequency compared to baseline (p = 0.0036). Conversely, no significant difference from baseline was observed for dogs receiving the placebo in the first study phase. These findings underscore the considerable variability in placebo responses observed in trials for canine epilepsy, contrasting with previous limited data. The identified phase effect should be carefully considered in the design and evaluation of canine epilepsy trials to ensure a more accurate assessment of efficacy for new treatments.

Indexed as

Dog DiseasesEpilepsyPlacebo EffectAnimalsAnticonvulsantsCross-Over StudiesDogsFemaleMaleProspective StudiesAnticonvulsantsCrossover trialsDogsEpilepsyHoneymoon effectPlacebo effectPlacebo response

Identifiers

PMID38783265
PMCPMC11119301

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.