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