Evidence map›Paper›PMID 29278279›Full record

Trial reportMovement disorders : official journal of the Movement Disorder Society2018

A randomized, double-blind, placebo-controlled trial of camicinal in Parkinson's disease.

Sarah L Marrinan, Tal Otiker, Lakshmi S Vasist, Rachel A Gibson, Bhopinder K Sarai, Matthew E Barton, Duncan B Richards, Per M Hellström, Dag Nyholm, George E Dukes and 1 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Movement disorders : official journal of the Movement Disorder Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Double-Blind, Randomized, Placebo-Controlled Trial of DA-9701 in Parkinson's Disease: PASS-GI Study.Movement disorders : official journal of the Movement Disorder Society · 2020
    Trial
  2. Article
  3. Review
  4. Management of Gastrointestinal Symptoms in Parkinson's Disease.Journal of central nervous system disease · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 3 countries.

Sarah L MarrinanRoyal Infirmary of Edinburgh, NHS Lothian, Edinburgh, United Kingdom.
Tal OtikerGlaxoSmithKline R&D, Stevenage, United Kingdom.
Lakshmi S VasistGlaxoSmithKline R&D, Research Triangle Park, North Carolina, United States.
Rachel A GibsonGlaxoSmithKline R&D, Stevenage, United Kingdom.
Bhopinder K SaraiGlaxoSmithKline, Cambridge, United Kingdom.
Matthew E BartonGlaxoSmithKline R&D, Research Triangle Park, North Carolina, United States.
Duncan B RichardsGlaxoSmithKline, Cambridge, United Kingdom.
Per M HellströmDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Dag NyholmDepartment of Neuroscience, Neurology, Uppsala University, Uppsala, Sweden.
George E DukesGlaxoSmithKline R&D, Research Triangle Park, North Carolina, United States.
David J BurnNewcastle University, Institute of Neurosciences, Newcastle upon Tyne, United Kingdom.
GlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (United States) · USUppsala University · SENewcastle University · GBResearch Triangle Park Foundation · USThe Neurosciences Foundation · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDelayed gastric emptying may impair l-dopa absorption, contributing to motor fluctuations. We evaluated the effect of camicinal (GSK962040), a gastroprokinetic, on the absorption of l-dopa and symptoms of PD.

methodsPhase II, double-blind, placebo-controlled trial. Participants were randomized to receive camicinal 50 mg once-daily (n = 38) or placebo (n = 20) for 7 to 9 days.

resultsl-dopa exposure was similar with coadministration of camicinal compared to placebo. Median time to maximum l-dopa concentration was reduced, indicating more rapid absorption of l-dopa. Camicinal resulted in significant reduction in OFF time (-2.31 hours; 95% confidence interval: -3.71, -0.90), significant increase in ON time (+1.88 hours; 95% confidence interval: 0.28, 3.48) per day, and significant decrease in mean total MDS-UPDRS score (-12.5; 95% confidence interval: -19.67, -5.29). Camicinal treatment was generally well tolerated.

conclusionsPD symptom improvement with camicinal occurred in parallel with more rapid absorption of l-dopa. This study provides evidence of an improvement of the motor response to l-dopa in people with PD treated with camicinal 50 mg once-daily compared with placebo, which will require further evaluation. © 2017 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Treatment OutcomeAdultAgedAged, 80 and overAnalysis of VarianceAntiparkinson AgentsArea Under CurveDose-Response Relationship, DrugDouble-Blind MethodFemaleFollow-Up StudiesHumansLevodopaMaleMiddle AgedParkinson DiseaseAntiparkinson AgentsLevodopaN-(3-fluorophenyl)-1-((4-(((3S)-3-methyl-1-piperazinyl)methyl)phenyl)acetyl)-4-piperidinaminePiperazinesPiperidinesClinical trials Randomized controlled (CONSORT agreement)Parkinson's disease/parkinsonism

Identifiers

PMID29278279
PMCPMC5838770
OpenAlexW2777737907

What OpenQuestion 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 OpenQuestion graph.