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An Extended-Release Form of Clonidine as an Anti-Manic Agent: An Add-on, Open-Label Study

Primary Purpose

Bipolar Disorder, Mania

Status
Terminated
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
extended-release clonidine
Sponsored by
Mclean Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder, Mania focused on measuring mania, clonidine, bipolar disorder

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • meet SCID criteria for bipolar disorder, type I, Mania with YMRS > 15
  • No significant improvement in symptoms after three or more days of hospitalization
  • documented medical evaluation without identified acute or serious medical illness
  • negative pregnancy test in women of child-bearing age

Exclusion Criteria:

  • involuntary commitment or lack of capacity to provide informed consent
  • low blood pressure

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    clonidine as an antimanic agent

    Arm Description

    Subjects with Bipolar Disorder, Mania receive an extended-release form of clonidine on the second day of this 3-day study. Rating scales, record of sleep, and a questionnaire of adverse effects is recorded on each of the three days.

    Outcomes

    Primary Outcome Measures

    Score on a Mania Rating Scale
    Mania rating scale to be performed each day of this 3 day study.

    Secondary Outcome Measures

    Full Information

    First Posted
    November 6, 2012
    Last Updated
    March 15, 2017
    Sponsor
    Mclean Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03065933
    Brief Title
    An Extended-Release Form of Clonidine as an Anti-Manic Agent: An Add-on, Open-Label Study
    Official Title
    An Extended-Release Form of Clonidine as an Anti-Manic Agent: An Add-On, Open-Label Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2017
    Overall Recruitment Status
    Terminated
    Study Start Date
    January 2012 (undefined)
    Primary Completion Date
    January 2013 (Actual)
    Study Completion Date
    January 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mclean Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The investigators plan to to study an extended-release form of clonidine, which the investigators hope will be even better tolerated than the immediate-release form, as an antimanic agent. Subjects will receive an extended-release form of clonidine in addition to their usual medication regimen on the second day of this three-day study. Rating scales, a record of sleep, and a questionnaire of adverse effects will be recorded on each of the 3 days. Any medication changes made by the attending psychiatrist and prns administered will be recorded throughout the study.
    Detailed Description
    Clonidine has been reported to be effective in a variety of hyperadrenergic states, including mania. It is generally well-tolerated and does not result in the severe adverse effects that are associated with many antipsychotics and mood stabilizers used in the treatment of mania, such as weight gain and akathisia. There is some suggestion that clonidine may be particularly effective in a subset of refractory cases and in patients who cannot tolerate antipsychotic medications or lithium. The investigators plan to to study an extended-release form of clonidine, which the investigators hope will be even better tolerated than the immediate-release form, as an antimanic agent. Subjects will receive an extended-release form of clonidine in addition to their usual medication regimen on the second day of this three-day study. Rating scales, a record of sleep, and a questionnaire of adverse effects will be recorded on each of the 3 days. Any medication changes made by the attending psychiatrist and prns administered will be recorded throughout the study. The investigators believe that studying as few as 10 subjects will give the investigators a sense as to whether the addition of clonidine is helpful in reducing manic symptoms and if the rate of adverse effects is unacceptable.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bipolar Disorder, Mania
    Keywords
    mania, clonidine, bipolar disorder

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Model Description
    Subjects with Bipolar Disorder, mania will receive an extended-release from of clonidine on the second day of this 3-day study. Rating scale, record of sleep, and a questionnaire of adverse effects will be recorded on each of the 3 days.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    5 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    clonidine as an antimanic agent
    Arm Type
    Experimental
    Arm Description
    Subjects with Bipolar Disorder, Mania receive an extended-release form of clonidine on the second day of this 3-day study. Rating scales, record of sleep, and a questionnaire of adverse effects is recorded on each of the three days.
    Intervention Type
    Drug
    Intervention Name(s)
    extended-release clonidine
    Other Intervention Name(s)
    Kapvay
    Intervention Description
    Subjects will received 0.2 mg extended-release clonidine twice on second day of this three-day study.
    Primary Outcome Measure Information:
    Title
    Score on a Mania Rating Scale
    Description
    Mania rating scale to be performed each day of this 3 day study.
    Time Frame
    3 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: meet SCID criteria for bipolar disorder, type I, Mania with YMRS > 15 No significant improvement in symptoms after three or more days of hospitalization documented medical evaluation without identified acute or serious medical illness negative pregnancy test in women of child-bearing age Exclusion Criteria: involuntary commitment or lack of capacity to provide informed consent low blood pressure
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Bruce Cohen, MD, PhD
    Organizational Affiliation
    Mclean Hospital
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    IPD to be shared via clinicaltrials.gov, publication, or personal request.

    Learn more about this trial

    An Extended-Release Form of Clonidine as an Anti-Manic Agent: An Add-on, Open-Label Study

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