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Comparison · NCT01308749-0ce29bf5

Sequence 2: Placebo:Oxytocin vs Sequence 1: Oxytocin:Oxytocin: Number of Participants Who Could Tolerate Twice Daily Oxytocin

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. Sequence 2: Placebo:Oxytocin vs Sequence 1: Oxytocin:Oxytocin: Number of Participants Who Could Tolerate Twice Daily Oxytocin. Trial comparisons, record NCT01308749-0ce29bf5. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01308749-0ce29bf5

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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 110.7721wilson
Risk in group 20.9170.6460.985wilson
Risk difference, group 1 minus group 20.0833-0.1550.354newcombe hybrid score
Risk ratio, group 1 over group 21.090.921.29log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on Sequence 2: Placebo:Oxytocin than on Sequence 1: Oxytocin:Oxytocin12from 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 1Sequence 2: Placebo:OxytocinIntervention: Drug: placebo double blind for 8 weeks then oxytocin open label for 8 weeks1313OG000
Group 2Sequence 1: Oxytocin:Oxytocin
Intervention: Drug: oxytocin = Syntocinon® Nasal Spray~total of 16 weeks exposure Subjects ages 3-10 years old will be titrated up to a maximum dose of 24IU. Subjects ages 11-17 years old will be titrated up to a maximum dose of 32IU.
1112OG001

Outcome

Type
PRIMARY
Title
Number of Participants Who Could Tolerate Twice Daily Oxytocin
Description
This study will help to determine tolerability of intranasal oxytocin treatment in children with autism by measuring the ability of at least 80% of the sample to tolerate twice daily intranasal administration of oxytocin.
Time frame
Week 0 to week 8
Population
This is over period 1, the double blind phase (week 0 to week 8) only

Source ClinicalTrials.gov

Trial

Title
A Study of Oxytocin in Children and Adolescents With Autistic Disorder
NCT number
NCT01308749
Phases
PHASE2
Conditions
Autism
Interventions
Oxytocin, Placebo
Lead sponsor
University of North Carolina, Chapel Hill
Results first posted
2017-07-17

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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