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Effect of Sarcosine on Symptomatology, Quality of Life, Oxidative Stress and Glutamatergic Parameters in Schizophrenia

NCT01503359, Phase 2, Completed, Medical University of Lodz

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleEffect of Sarcosine on Symptomatology, Quality of Life, Oxidative Stress and Glutamatergic Parameters in SchizophreniaClinicalTrials.gov
NCT numberNCT01503359ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesPhase 2ClinicalTrials.gov
Enrollment70 participants, estimatedClinicalTrials.gov
Lead sponsorMedical University of LodzClinicalTrials.gov
ConditionsSchizophreniaClinicalTrials.gov
InterventionsSarcosineClinicalTrials.gov
First posted2012-01-04ClinicalTrials.gov
Last updated2016-09-16ClinicalTrials.gov

Registered outcomes 8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryAssessment of sarcosine vs. placebo impact on schizophrenia symptoms using Positive and Negative Syndrome Scale (PANSS).6 monthsBoth arms, every visitClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on the parameters of quality of life (QoL) and sexual functioning.6 monthsBoth arms, every visitClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on depressive symptoms using Calgary Depression Scale for Schizophrenia.6 monthsBoth arms, every visitClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on cognitive functions using Wisconsin Card Sort Test, Trail Making Test and Stroop Test.6 monthsBoth arms, before and after taking sarcosine or placeboClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on oxidative stress parameters (T-BARS).6 monthsBoth arms, before and after taking sarcosine or placeboClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on brain metabolism parameters (magnetic resonance spectroscopy).6 monthsBoth arms, before and after taking sarcosine or placeboClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on oculomotoric parameters (saccadic and antisaccadic task in electrooculography).6 monthsBoth arms, before and after taking sarcosine or placeboClinicalTrials.gov
SecondaryImpact assessment of sarcosine versus placebo on blood levels of glycine, sarcosine, BDNF and MMP-9.6 monthsBoth arms, before and after taking sarcosine or placeboClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 22

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
1654746BACKGROUNDPubMed
1695402BACKGROUNDPubMed
7751957BACKGROUNDPubMed
8036251BACKGROUNDPubMed
9384954BACKGROUNDPubMed
9798069BACKGROUNDPubMed
10628529BACKGROUNDPubMed
10719161BACKGROUNDPubMed
10873924BACKGROUNDPubMed
11532718BACKGROUNDPubMed
11588613BACKGROUNDPubMed
11806864BACKGROUNDPubMed
14684435BACKGROUNDPubMed
15023571BACKGROUNDPubMed
15502972BACKGROUNDPubMed
15708298BACKGROUNDPubMed
16625590BACKGROUNDPubMed
16780811BACKGROUNDPubMed
17659263BACKGROUNDPubMed
26306650DERIVEDPubMed

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 3

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)