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Trial · NCT02930005

Pentosan Polysulfate Sodium and Meclofenamic Acid as Treatments in Patients With Psychotic Disorders

NCT02930005, Phase 2, Completed, The University of Texas Health Science Center, Houston; results first posted 2019-03-26

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pentosan Polysulfate Sodium and Meclofenamic Acid as Treatments in Patients With Psychotic Disorders. Trials, record NCT02930005. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02930005

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Trial

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

Title
Pentosan Polysulfate Sodium and Meclofenamic Acid as Treatments in Patients With Psychotic Disorders
NCT number
NCT02930005
Status
Completed
Phases
Phase 2
Enrollment
8 participants, actual
Lead sponsor
The University of Texas Health Science Center, Houston
Conditions
Psychotic Disorders, Schizophrenia, Schizoaffective Disorder, Bipolar Disorder
Interventions
Meclofenamic acid, Pentosan polysulfate sodium
First posted
2016-10-11
Last updated
2019-03-26
Results first posted
2019-03-26

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryChange in Cognitive Function as Assessed by the NIH Toolbox Cognitive Test Battery (NCTB) Composite Scorebaseline, 8 weeks
A higher composite score on the NCTB indicates better cognitive performance. The NCTB consists of 7 tests and 8 sub-scores, and the NIH Toolbox software calculates total composite score by averaging the normalized scores of each subscale and then deriving scale scores. The "NIH Toolbox Scoring and Interpretation Guide" (found online) doesn't indicate a total composite score range (because the score ranges are infinite), but describes scoring as follows: To get a normalized composite score, the score of the test taker is compared to the scores in the NIH Toolbox nationally representative normative sample. The mean score is 100 and the standard deviation (SD) is 15. A score at or near 100 indicates average ability compared with others. Scores around 115 suggest above-average ability. Scores around 130 suggest superior ability (in the top 2 percent nationally). A score around 85 suggests below-average ability. A score in the range of 70 or below suggests significant impairment.
SecondaryChange in Severity of Psychotic Symptoms as Assessed by Positive and Negative Syndrome Scale (PANSS)baseline, 8 weeksChange in the Positive and Negative Syndrome Scale (PANSS) total score after 8 weeks. The range of scores on the PANSS is 30 to 210, with higher scores associated with better outcomes.

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Cognitive Function as Assessed by the NIH Toolbox Cognitive Test Battery (NCTB) Composite Scorebaseline, 8 weeksscoreNUMBER
SECONDARYChange in Severity of Psychotic Symptoms as Assessed by Positive and Negative Syndrome Scale (PANSS)baseline, 8 weeksscoreNUMBER

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Change in Cognitive Function as Assessed by the NIH Toolbox Cognitive Test Battery (NCTB) Composite ScoreMeclofenamic Acid31.96score
Change in Cognitive Function as Assessed by the NIH Toolbox Cognitive Test Battery (NCTB) Composite ScorePentosan Polysulfate Sodium0.96score
Change in Severity of Psychotic Symptoms as Assessed by Positive and Negative Syndrome Scale (PANSS)Meclofenamic Acid-11score
Change in Severity of Psychotic Symptoms as Assessed by Positive and Negative Syndrome Scale (PANSS)Pentosan Polysulfate Sodium-22score

Participant flow8

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMeclofenamic Acid2
Overall StudySTARTEDPentosan Polysulfate Sodium6
Overall StudyCompleted 2 WeeksMeclofenamic Acid2
Overall StudyCompleted 2 WeeksPentosan Polysulfate Sodium2
Overall StudyCOMPLETEDMeclofenamic Acid1
Overall StudyCOMPLETEDPentosan Polysulfate Sodium1
Overall StudyNOT COMPLETEDMeclofenamic Acid1
Overall StudyNOT COMPLETEDPentosan Polysulfate Sodium5

Adverse events2

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHyperglycemiaEndocrine disordersMeclofenamic Acid020
otherHyperglycemiaEndocrine disordersPentosan Polysulfate Sodium161

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMeclofenamic Acid02
Total, all-cause mortalityPentosan Polysulfate Sodium06
Total, other adverse eventsMeclofenamic Acid02
Total, other adverse eventsPentosan Polysulfate Sodium16
Total, serious adverse eventsMeclofenamic Acid02
Total, serious adverse eventsPentosan Polysulfate Sodium06

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

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.

None in this release.

Trial comparisons2

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

ComparisonSource
Meclofenamic Acid vs Pentosan Polysulfate Sodium: deaths from any causeTrial comparisons
Meclofenamic Acid vs Pentosan Polysulfate Sodium: serious adverse eventsTrial comparisons

Tests0

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

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02930005

GET https://conductscience.org/api/trials/v1/NCT02930005/registered