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Trial record 2 of 4 for:    omega-3 prodromal

Ethyl-EPA Treatment of Prodromal Patients

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00634361
Recruitment Status : Completed
First Posted : March 13, 2008
Last Update Posted : May 22, 2014
Sponsor:
Information provided by (Responsible Party):
Yale University

Brief Summary:
This is an open-label trial of an omega-3 fatty acid for symptoms of the schizophrenia prodrome.

Condition or disease Intervention/treatment Phase
Schizophrenia Prodrome Drug: ethyl-eicosapentaenoic acid Phase 2 Phase 3

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 7 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Ethyl-EPA Treatment of Prodromal Patients
Study Start Date : September 2001
Primary Completion Date : August 2005
Study Completion Date : August 2005

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Schizophrenia
U.S. FDA Resources

Arm Intervention/treatment
Experimental: A Drug: ethyl-eicosapentaenoic acid
2 mg per day
Other Name: ethyl-EPA, an omega-3 fatty acid



Primary Outcome Measures :
  1. conversion to psychosis [ Time Frame: one year ]


Information from the National Library of Medicine

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Ages Eligible for Study:   14 Years to 35 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • meets criteria for schizophrenia prodrome

Exclusion Criteria:

  • any lifetime antipsychotic treatment

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00634361


Sponsors and Collaborators
Yale University
Investigators
Principal Investigator: Scott W Woods, MD Yale University

Responsible Party: Yale University
ClinicalTrials.gov Identifier: NCT00634361     History of Changes
Obsolete Identifiers: NCT00237835
Other Study ID Numbers: LA01.03.0011
First Posted: March 13, 2008    Key Record Dates
Last Update Posted: May 22, 2014
Last Verified: May 2014

Additional relevant MeSH terms:
Schizophrenia
Schizophrenia Spectrum and Other Psychotic Disorders
Mental Disorders