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Study · Randomized controlled trial · n = 40 · 2013

5 results

Intranasal oxytocin as an adjunct to risperidone in patients with schizophrenia : an 8-week, randomized, double-blind, placebo-controlled study.

Modabbernia A, Rezaei F, Salehi B, Salehi B, Jafarinia M, Ashrafi M, Tabrizi M, Hosseini SM, Tajdini M, Ghaleiha A, Akhondzadeh S

CNS drugs1 Jan 2013Cited by 85 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study5

5 results from studies that gave the peptide. 5 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In patients with schizophrenia on risperidone, adjunct intranasal oxytocin improved the PANSS positive subscale more than placebo by week 8.

    In plain wordsIn people with schizophrenia taking risperidone, oxytocin spray improved positive symptoms more than placebo after 8 weeks.

    Peptide
    Oxytocin
    Outcome
    DecreasePANSS positive subscale reduction at week 8
    Study

    n = 40

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Anxiety and mood · Mental health and mood
    Studied dose
    20 IU twice daily in week 1, then 40 IU twice daily · intranasal · 8 weeksAs given in this study (human).

    Measurements

    Cohen's d
    1.2 NA
    PANSS positive
    Score reduction
    20%
    oxytocin
    Score reduction
    4%
    placebo

    Source sentences

    Summary
    By week 8, patients in the oxytocin group showed significantly greater improvement on the positive (Cohen's d = 1.2, 20 % vs. 4 % reduction in score, p < 0.001)
    2 context sentences
    Summary · context
    Forty patients (male and female gender) aged 18-50 years with a diagnosis of schizophrenia (DSM-IV-TR) who were on a stable dose of risperidone for a minimum of 1 month and who were chronically partially responsive to antipsychotic monotherapy were included in the study.
    Summary · context
    The patients were randomly assigned to oxytocin intranasal spray (Syntocinon(®); Novartis, Basel, Switzerland) or placebo intranasal spray containing normal saline (ACER, Tehran, Iran) for 8 weeks. Oxytocin spray was administered as 20 IU (five sprays) twice a day for the first week followed by 40 I…
  2. 02HumanRandomized controlled trialEfficacy outcome

    In patients with schizophrenia on risperidone, adjunct intranasal oxytocin improved the PANSS negative subscale more than placebo by week 8.

    In plain wordsIn people with schizophrenia taking risperidone, oxytocin spray improved negative symptoms more than placebo after 8 weeks.

    Peptide
    Oxytocin
    Outcome
    DecreasePANSS negative subscale reduction at week 8
    Study

    n = 40

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Anxiety and mood · Mental health and mood
    Studied dose
    20 IU twice daily in week 1, then 40 IU twice daily · intranasal · 8 weeksAs given in this study (human).

    Measurements

    Cohen's d
    1.4 NA
    PANSS negative
    Score reduction
    7%
    oxytocin
    Score reduction
    2%
    placebo

    Source sentences

    Summary
    negative (Cohen's d = 1.4, 7 % vs. 2 % reduction in score, p < 0.001)
    2 context sentences
    Summary · context
    Forty patients (male and female gender) aged 18-50 years with a diagnosis of schizophrenia (DSM-IV-TR) who were on a stable dose of risperidone for a minimum of 1 month and who were chronically partially responsive to antipsychotic monotherapy were included in the study.
    Summary · context
    The patients were randomly assigned to oxytocin intranasal spray (Syntocinon(®); Novartis, Basel, Switzerland) or placebo intranasal spray containing normal saline (ACER, Tehran, Iran) for 8 weeks. Oxytocin spray was administered as 20 IU (five sprays) twice a day for the first week followed by 40 I…
  3. 03HumanRandomized controlled trialEfficacy outcome

    In patients with schizophrenia on risperidone, adjunct intranasal oxytocin improved the PANSS general psychopathology subscale more than placebo by week 8.

    In plain wordsIn people with schizophrenia taking risperidone, oxytocin spray improved general symptoms more than placebo after 8 weeks.

    Peptide
    Oxytocin
    Outcome
    DecreasePANSS general psychopathology reduction at week 8
    Study

    n = 40

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Anxiety and mood · Mental health and mood
    Studied dose
    20 IU twice daily in week 1, then 40 IU twice daily · intranasal · 8 weeksAs given in this study (human).

    Measurements

    Cohen's d
    0.8 NA
    PANSS general
    Score reduction
    8%
    oxytocin
    Score reduction
    2%
    placebo

    Source sentences

    Summary
    general psychopathology (Cohen's d = 0.8, 8 % vs. 2 % reduction in score, p = 0.021)
    2 context sentences
    Summary · context
    Forty patients (male and female gender) aged 18-50 years with a diagnosis of schizophrenia (DSM-IV-TR) who were on a stable dose of risperidone for a minimum of 1 month and who were chronically partially responsive to antipsychotic monotherapy were included in the study.
    Summary · context
    The patients were randomly assigned to oxytocin intranasal spray (Syntocinon(®); Novartis, Basel, Switzerland) or placebo intranasal spray containing normal saline (ACER, Tehran, Iran) for 8 weeks. Oxytocin spray was administered as 20 IU (five sprays) twice a day for the first week followed by 40 I…
  4. 04HumanRandomized controlled trialEfficacy outcome

    In patients with schizophrenia on risperidone, adjunct intranasal oxytocin improved the PANSS total score more than placebo by week 8.

    In plain wordsIn people with schizophrenia taking risperidone, oxytocin spray improved overall symptom scores more than placebo after 8 weeks.

    Peptide
    Oxytocin
    Outcome
    DecreasePANSS total score reduction at week 8
    Study

    n = 40

    Comparator
    Placebo
    Analysis
    Primary
    Outcome group
    Anxiety and mood · Mental health and mood
    Studied dose
    20 IU twice daily in week 1, then 40 IU twice daily · intranasal · 8 weeksAs given in this study (human).

    Measurements

    Cohen's d
    1.9 NA
    PANSS total
    Score reduction
    11%
    oxytocin
    Score reduction
    2%
    placebo

    Source sentences

    Summary
    total (Cohen's d = 1.9, 11 % vs. 2 % reduction in score, p < 0.001) PANSS scores than the placebo group.
    2 context sentences
    Summary · context
    Forty patients (male and female gender) aged 18-50 years with a diagnosis of schizophrenia (DSM-IV-TR) who were on a stable dose of risperidone for a minimum of 1 month and who were chronically partially responsive to antipsychotic monotherapy were included in the study.
    Summary · context
    The patients were randomly assigned to oxytocin intranasal spray (Syntocinon(®); Novartis, Basel, Switzerland) or placebo intranasal spray containing normal saline (ACER, Tehran, Iran) for 8 weeks. Oxytocin spray was administered as 20 IU (five sprays) twice a day for the first week followed by 40 I…
  5. 05HumanRandomized controlled trialSafety outcome

    In patients with schizophrenia on risperidone, adverse effects, including sodium concentration change, were similar between oxytocin and placebo.

    In plain wordsIn people with schizophrenia taking risperidone, side effects with oxytocin spray were similar to placebo.

    Peptide
    Oxytocin
    Outcome
    No significant changeAdverse effects including sodium concentration change
    Study

    n = 40

    Comparator
    Placebo
    Outcome group
    Adverse events · Mental health and mood
    Studied dose
    20 IU twice daily in week 1, then 40 IU twice daily · intranasal · 8 weeksAs given in this study (human).

    Source sentences

    Summary
    Adverse effects including the sodium concentration change were similar between the two groups.
    2 context sentences
    Summary · context
    Forty patients (male and female gender) aged 18-50 years with a diagnosis of schizophrenia (DSM-IV-TR) who were on a stable dose of risperidone for a minimum of 1 month and who were chronically partially responsive to antipsychotic monotherapy were included in the study.
    Summary · context
    The patients were randomly assigned to oxytocin intranasal spray (Syntocinon(®); Novartis, Basel, Switzerland) or placebo intranasal spray containing normal saline (ACER, Tehran, Iran) for 8 weeks. Oxytocin spray was administered as 20 IU (five sprays) twice a day for the first week followed by 40 I…

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    11 Oct 2026, 01:30 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 02:49 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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