Evidence map›Paper›PMID 26230671›Full record

Trial reportMovement disorders : official journal of the Movement Disorder Society2015

A randomized, double-blind phase I/IIa study of intranasal glutathione in Parkinson's disease.

Laurie K Mischley, James B Leverenz, Richard C Lau, Nayak L Polissar, Moni B Neradilek, Ali Samii, Leanna J Standish

Abstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Movement disorders : official journal of the Movement Disorder Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  11. Nose-to-brain drug delivery: from bench to bedside.Translational neurodegeneration · 2025
    Review
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  15. Research progress on intranasal treatment for Parkinson's disease.Neuroprotection (Chichester, England) · 2024
    Review
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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

7 authors at 5 institutions in 2 countries.

Laurie K MischleyBastyr University Research Institute, Kenmore, Washington, USA.
James B LeverenzCleveland Lou Ruvo Center for Brain Health, Cleveland Clinic, Cleveland, Ohio, USA.
Richard C LauBastyr University Research Institute, Kenmore, Washington, USA.
Nayak L PolissarThe Mountain-Whisper Light, Seattle, Washington, USA.
Moni B NeradilekThe Mountain-Whisper Light, Seattle, Washington, USA.
Ali SamiiDepartment of Neurology, University of Washington; Northwest PADRECC at the Seattle VA Medical Center, Washington, USA.
Leanna J StandishBastyr University Research Institute, Kenmore, Washington, USA.
The Mountain Institute · USUniversity of Washington · USBastyr University · USCleveland Clinic · USOregon State University · US

Funding

Udall Center Director's meeting poster awardP50NS062684 · NINDS · UNIVERSITY OF WASHINGTON · PI MONTINE, THOMAS J · 2009 to 2020
$18.3M
Intranasal Glutathione in Parkinson's DiseaseK01AT004404 · NCCIH · BASTYR UNIVERSITY · PI MISCHLEY, LAURIE KATHERN · 2010 to 2014
$589k
NCCIH NIH HHS K01 AT004404NCCIH NIH HHS K01AT04404NINDS NIH HHS P50 NS062684NINDS NIH HHS P50NS062684
6 · The paper itself

Abstract

backgroundDepletion of reduced glutathione is associated with PD and glutathione augmentation has been proposed as a disease-modifying strategy. The aim of this study was to determine the safety and tolerability of intranasal reduced glutathione in individuals with PD.

methodsThirty individuals with PD were randomized to either placebo (saline), 300 mg/day, or 600 mg/day of intranasal glutathione in three divided daily doses. Follow-up visits included side effect screening of PD symptoms and cognition, blood chemistry, sinus irritation, and hyposmia. Tolerability was measured by frequency and severity of reported adverse events, compliance, and withdrawals from the study.

resultsAfter 3 months, there were no substantial differences between groups in the number of adverse events reported or observed among all safety measures assessed. All groups met tolerability criteria.

conclusionsThese data support the safety and tolerability of intranasal glutathione in this population. Pharmacokinetic and dose-finding studies are warranted.

Indexed as

Administration, IntranasalAntiparasitic AgentsDose-Response Relationship, DrugDouble-Blind MethodFemaleFollow-Up StudiesGlutathioneHumansMaleParkinson DiseaseSeverity of Illness IndexTreatment OutcomeAntiparasitic AgentsGlutathioneantioxidantdeficiencyglutathioneneuroprotectionnutrition

Identifiers

PMID26230671
PMCPMC4609266
OpenAlexW1898391015

What OpenQuestion holds

Textmetadata
LicenceTDM
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.