Evidence map›Paper›PMID 27521437›Full record

Trial reportNeurology2016

Adjunctive pregabalin vs gabapentin for focal seizures: Interpretation of comparative outcomes.

Jacqueline French, Paul Glue, Daniel Friedman, Mary Almas, Nandan Yardi, Lloyd Knapp, Verne Pitman, Holly B Posner

Registry-linked trialOpen access · hybridAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00537940 (A Randomized, Double-blind, Parallel-group Multi-center Comparative Flexible-dose Trial Of Pregabalin Versus Gabapentin As Adjunctive Therapy In Subjects With Partial Seizures.), which is not on this map. Cited by 10 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 5 pooled it
1.6field-weighted citation impact, top 17% 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.

NCT00537940 phase4completednot on this map

A Randomized, Double-blind, Parallel-group Multi-center Comparative Flexible-dose Trial Of Pregabalin Versus Gabapentin As Adjunctive Therapy In Subjects With Partial Seizures.

TypeinterventionalSponsorPfizer's Upjohn has merged with Mylan to form Viatris Inc.Ran2008 to 2013Enrolled482ConditionsEpilepsy, Partial Seizure Disorder, Epilepsies, Partial, Complex Partial Seizure DisorderArmsPregabalin, Gabapentin
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 5 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pregabalin add-on for drug-resistant focal epilepsy.The Cochrane database of systematic reviews · 2022
    Pooled it
  3. Gabapentin add-on treatment for drug-resistant focal epilepsy.The Cochrane database of systematic reviews · 2021
    Pooled it
  4. Pregabalin add-on for drug-resistant focal epilepsy.The Cochrane database of systematic reviews · 2019
    Pooled it
  5. Gabapentin add-on treatment for drug-resistant focal epilepsy.The Cochrane database of systematic reviews · 2018
    Pooled it
  6. Article
  7. Article
  8. Article
  9. Efficacy and tolerability of antiseizure drugs.Therapeutic advances in neurological disorders · 2021
    Review
  10. Article
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.

Jacqueline FrenchFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT. Jacqueline.French@nyumc.org.
Paul GlueFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Daniel FriedmanFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Mary AlmasFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Nandan YardiFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Lloyd KnappFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Verne PitmanFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
Holly B PosnerFrom the NYU Comprehensive Epilepsy Center (J.F., D.F.), New York, NY; Department of Psychological Medicine, Dunedin School of Medicine, University of Otago (P.G.), New Zealand; Global Product Development, Pfizer Inc. (M.A., H.B.P.), New York, NY; Yardi Epilepsy Clinic, KEM and Vatsal Hospital (N.Y.), Pune, India; and Global Product Development, Pfizer Inc. (L.K., V.P.), Groton, CT.
University of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the comparative safety and adjunctive efficacy of pregabalin and gabapentin in reducing seizure frequency in patients with partial-onset seizures based on prestudy modeling showing superior efficacy for pregabalin.

methodsThe design of this comparative efficacy and safety study of pregabalin and gabapentin as adjunctive treatment in adults with refractory partial-onset seizures was randomized, flexible dose, double blind, and parallel group. The study included a 6-week baseline and a 21-week treatment phase. The primary endpoint was the percentage change from baseline in 28-day seizure rate to the treatment phase.

resultsA total of 484 patients were randomized to pregabalin (n = 242) or gabapentin (n = 242). Of these, 359 patients (187 pregabalin, 172 gabapentin) completed the treatment phase. The observed median and mean in percentage change from baseline was -58.65 and -47.7 (SD 48.3) for pregabalin and -57.43 and -45.28 (SD 60.6) for gabapentin. For the primary endpoint, there was no significant difference between treatments. The Hodges-Lehman estimated median difference was 0.0 (95% confidence interval -6.0 to 7.0). Safety profiles were comparable and consistent with prior trials.

conclusionsThe absence of the anticipated efficacy difference based on modeling of prior, nearly identical trials and the larger-than-expected response rates of the 2 antiepileptic drugs were unexpected. These findings raise questions that are potentially important to consider in future comparative efficacy trials. CLINICALTRIALSGOV IDENTIFIER: NCT00537940. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that for patients with partial seizures enrolled in this study, pregabalin is not superior to gabapentin in reducing seizure frequency. Because of the atypical response rates, the results of this study are poorly generalizable to other epilepsy populations.

Indexed as

AdolescentAdultAgedAged, 80 and overAminesAnticonvulsantsChildCyclohexanecarboxylic AcidsDouble-Blind MethodDrug Resistant EpilepsyDrug Therapy, CombinationEpilepsies, PartialFemaleGabapentingamma-Aminobutyric AcidHumansAminesAnticonvulsantsCyclohexanecarboxylic AcidsGabapentingamma-Aminobutyric AcidPregabalin

Identifiers

PMID27521437
PMCPMC5035985
OpenAlexW2516435552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.