Community Academic Profiles

Charles DeBattista

Ropinirole Controlled Release (CR) as an Adjunctive Agent in the Treatment of Major Depression

Contact Information

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Jessica Hawkins (650) 723-8323
To view all clinical trials at Stanford, please see the Clinical Trials Directory.

Brief

This is an 8 week study for patients who are currently taking antidepressant medication but not fully responding. Ropinirole CR would be taken in conjunction with current antidepressant medication. Patients come into the clinic once a week when starting on the medication and then once every other week for the remainder of the 8 weeks.

Recruiting Status:

Completed

Stanford Recruiting Status:

No longer recruiting

Intervention(s):

  • Drug: Ropinirole CR

Phase:

N/A

Eligibility

Ages Eligible for Study:

18 years to 65 years

Genders Eligible for Study:

Male and Female

Health of Volunteers:

People with the conditions listed in this trial can participate as controls.

Key Inclusion Criteria:

1. Age 18 to 65 years old
2. Currently experiencing major depression
3. On at least an adequate dose of fluoxetine, paroxetine, sertraline, citalopram, escitalopram, venlafaxine, bupropion, mirtazapine or duloxetine for at least 6 weeks (monotherapy).

Key Exclusion Criteria:

1. Pregnant females or females of child bearing years not using adequate birth control in the opinion of the investigators
2. Known sensitivity to ropinirole
3. Significant medical conditions that would preclude safe participation in the study in the opinion of the investigators.
4. Significant abnormalities observed in screening laboratory evaluation

Additional Study Details

Official Title:

Ropinirole Controlled Release (CR) as an Adjunctive Agent in the Treatment of Major Depression

Anticipated start date:

1/1/2006

Lead Sponsor:

Stanford University

Collaborator(s):

  • Duke University
  • GSK

Investigator(s):

Study Type:

Interventional

Purpose:

Treatment

Allocation:

Non-randomized

Masking:

Open

Control:

none

Assignment:

Single Group

Endpoints:

Safety/Efficacy

Primary Outcomes:

  • HamD

Secondary Outcomes:

  • MADRS

Total Number to be Enrolled:

60

Total Number to be Enrolled at Stanford:

30

More Information

Trial Unique Id: 2969

Locations & Contacts

Stanford Locations & Contacts:

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Primary Contact:

Jessica Hawkins (650) 723-8323

Non-Stanford Locations:

This study is being conducted at multiple locations, including non-Stanford locations.

This listing was last updated:

5/14/2008

PLEASE NOTE:

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers are provided for obtaining additional information on specific clinical research trials only. If you have specific questions which require clinical expertise, please call your primary care physician. If you do not have a primary care physician please feel free to call the SHC Physician Referral Service at (800) 756-9000 or send an email.

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