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Oxytocin Add on Study for Stable Schizophrenic Patients

NCT00506909 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2019-09-25

Study results available
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Summary

The objective of the study is to compare the efficacy of intranasal oxytocin versus intranasal placebo to improve symptoms in schizophrenia patients who have residual symptoms despite being on adequate treatment with antipsychotic medication.

Conditions

Interventions

DRUG

Oxytocin

20 IU BID or 40 IU BID

DRUG

Placebo

20 IU BID or 40 IU BID

Sponsors & Collaborators

  • Stanley Medical Research Institute

    collaborator OTHER

  • David Feifel

    lead OTHER

Principal Investigators

  • David Feifel, MD, PhD · University of California, San Diego

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2014-03-31
Completion
2014-03-31

Countries

  • United States

Study Locations

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Entities

Drugs
Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00506909 on ClinicalTrials.gov