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Comparison · NCT00330863-e25ca1bb

Injectable vs Oral: Number of Patients Discontinuing From the Study

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Injectable vs Oral: Number of Patients Discontinuing From the Study. Trial comparisons, record NCT00330863-e25ca1bb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00330863-e25ca1bb

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.5290.4510.607wilson
Risk in group 20.5260.4470.604wilson
Risk difference, group 1 minus group 20.0031-0.1080.114newcombe hybrid score
Risk ratio, group 1 over group 21.010.8131.24log
Odds ratio, group 1 over group 21.010.6461.59log
Number needed to treat, for one more participant with the outcome on Injectable than on Oral323from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1InjectableParticipants assigned to receive long-acting injectable risperidone~Risperidone microspheres: Minimum dose is 12.5 mg every 2 weeks. Maximum dose is 75 mg every 2 weeks.81153OG000
Group 2Oral
Participants assigned to receive oral atypical antipsychotic medication~Risperidone: Target dose is 4 mg/day.~Olanzapine: Target dose is 15 mg/day.~Quetiapine: Target dose is 600 mg/day.~Ziprasidone: Target dose is 120 mg/day.~Aripiprazole: Target dose is 20 mg/day.~Paliperidone: Target dose is 6 mg/day.
80152OG001

Outcome

Type
SECONDARY
Title
Number of Patients Discontinuing From the Study
Description
Time frame
Measured throughout study up to 30 months
Population

Source ClinicalTrials.gov

Trial

Title
Preventing Relapse in Schizophrenia: Oral Antipsychotics Compared To Injectables: Evaluating Efficacy
NCT number
NCT00330863
Phases
PHASE4
Conditions
Schizophrenia, Schizoaffective Disorder
Interventions
Risperidone microspheres, Risperidone, Olanzapine, Quetiapine, Ziprasidone, Aripiprazole, Paliperidone
Lead sponsor
Northwell Health
Results first posted
2018-07-10

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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