Intranasal Oxytocin in the Treatment of Autism

Completed · Phase 2 · Has a placebo group

Conditions studied: Autism

In brief

The purpose of this study is to learn whether or not the drug called oxytocin is helpful in improving mood and social functioning in adults with autism.

Key facts

Study ID

NCT00490802

Run by

Evdokia Anagnostou

People needed

19

Starts

2006-06-01

Expected to finish

2012-04-01

Last updated by the study team

2015-10-23

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female outpatients 18 to 60 years of age.
• Meet Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision. The diagnosis will be confirmed with Autism Diagnostic Interview-Revised and Autism Diagnostic Observation Schedule .
• Have a Clinician's Global Impression-Severity score ≥ 4 (moderately ill) at Screening and Baseline.
• If already receiving stable nonpharmacologic educational, behavioral, and/or dietary interventions, have continuous participation during the preceding 3 months prior to Screening and will not electively initiate new or modify ongoing interventions for the duration of the study.
• Have normal physical examination and laboratory test results at Screening. If abnormal, the finding(s) must be deemed clinically insignificant by the Investigators.
• The patient must be able to speak and understand English sufficiently to understand the nature of the study and to allow for the completion of all study assessments.
• Have a normal Intelligence Quotient (>70) supported by the Wechsler Abbreviated Scales of Intelligence.

You may not qualify if…

• Patients born prior to 35 weeks gestational age.
• Patients with any primary psychiatric diagnosis other than autism at Screening: a history of attention deficit hyperactivity disorder, bipolar disorder, psychosis, posttraumatic stress disorder, schizophrenia, or major depressive disorder.
• Patients with a medical history of neurological disease, including, but not limited to, epilepsy/seizure disorder (except simple febrile seizures), movement disorder, tuberous sclerosis, fragile X, and any other known genetic syndromes, or known abnormal magnetic resonance imaging/structural lesion of the brain.
• Pregnant female patients.
• Patients with a medical condition that might interfere with the conduct of the study, confound interpretation of the study results, or endanger their own well-being. Patients with evidence or history of malignancy or any significant hematological, endocrine, cardiovascular (including any rhythm disorder), respiratory, renal, hepatic, or gastrointestinal disease.
• Patients taking psychoactive medication(s) (e.g., stimulants, antidepressants, antipsychotics, antiepileptics, anxiolytics, clonidine).
• Patients who plan to initiate or change nonpharmacologic interventions during the course of the study.
• Patients unable to tolerate venipuncture procedures for blood sampling.
• Patients who, in the Investigator's opinion, might not be suitable for the study.

Where it is running

• Mount Sinai School of Medicine — New York, New York, United States

Full record on ClinicalTrials.gov

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