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Trial · NCT03304457

Lurasidone Vs Olanzapine on Neurotrophic Biomarkers and Cardiometabolic Parameters in Unmedicated Schizophrenia

NCT03304457, Phase 4, Completed, All India Institute of Medical Sciences, Bhubaneswar

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Lurasidone Vs Olanzapine on Neurotrophic Biomarkers and Cardiometabolic Parameters in Unmedicated Schizophrenia. Trials, record NCT03304457. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03304457

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Trial

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

Title
Lurasidone Vs Olanzapine on Neurotrophic Biomarkers and Cardiometabolic Parameters in Unmedicated Schizophrenia
NCT number
NCT03304457
Status
Completed
Phases
Phase 4
Enrollment
100 participants, actual
Lead sponsor
All India Institute of Medical Sciences, Bhubaneswar
Conditions
Schizophrenia
Interventions
Olanzapine, Lurasidone
First posted
2017-10-09
Last updated
2020-03-31

Source ClinicalTrials.gov

Registered outcomes14

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

ListOutcomeTime frameDescription
PrimarySerum brain derived neurotrophic factor (BDNF)6 weeksthe change in serum level of BDNF from baseline after treatment with lurasidone or olanzapine
Secondaryserum nerve growth factor (NGF)6 weeksthe change in serum level of NGF from baseline after treatment with lurasidone or olanzapine
SecondarySerum Neurotrophin 3 (NT3)6 weeksthe change in serum level of NT3 from baseline after treatment with lurasidone or olanzapine
SecondaryPANSS score6 weeksTo determine the association (if any) between change in serum neurotrophic factor and PANSS score
SecondarySocial and occupational functioning assessment scale (SOFAS)6 weeksTo determine the association (if any) between change in serum neurotrophic factor and SOFAS (Social and occupational functioning assessment scale) score
SecondarySerum hsCRP6 weeksto assess cardiovascular risk in schizophrenia
SecondarySerum Insulin6 weeksto assess insulin resistance
SecondaryLDL/HDL ratio6 weeksto assess dyslipidemia and cardiovascular risk
SecondaryFasting blood sugar6 weeksto assess dysglycemia
SecondaryGlycosylated Hemoglobin (HbA1c)6 weeksto assess dysglycemia

Outcomes0

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

None in this release.

Results by group0

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

None in this release.

Participant flow0

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

None in this release.

Adverse events0

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

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers14

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
11383973RESULTPubMed
16829550RESULTPubMed
17006758RESULTPubMed
17159456RESULTPubMed
17459549RESULTPubMed
18791076RESULTPubMed
20218790RESULTPubMed
20568658RESULTPubMed
21357874RESULTPubMed
21639796RESULTPubMed

1 to 10 of 14

See all 14 papers

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 comparisons0

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

None in this release.

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/NCT03304457

GET https://conductscience.org/api/trials/v1/NCT03304457/registered