Carbamazepine Extended-Release for the Treatment of Bipolar Depression

NCT ID: NCT00203567

Last Updated: 2008-06-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 25 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-08-31
• Study Completion Date: 2008-05-31

Brief Summary

To study the efficacy and safety of beaded extended-release Carbamazepine (Equetro) in the treatment of patients with Bipolar Disorder with a Major Depressive Episode.

Detailed Description

Patients with Bipolar I or II Disorder with a Major Depressive Episode who sign informed consent and meet eligibility criteria will begin treatment with extended release carbamazepine (ERC-CBZ ). The dose of ERC-CBZ will be initiated at 200mg twice daily and increased as tolerated by 200mg/day every 3 days up to 1200mg/day by week 2 (target dose). Then the dose may be increased at the investigator's discretion, up to1600mg/day as tolerated by week 8, if needed for a greater therapeutic response. Efficacy will be assessed biweekly with the Montgomery-Asberg Depression Rating Scale (MADRS) and Clinical Global Impression-Bipolar (CGI-BP). Safety is assessed biweekly with adverse events self-reports and laboratory evaluations. ).

Conditions

Bipolar Depression

Keywords

bipolar depression; carbamazepine ER; Equetro

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Equetro

Equetro

Group Type: ACTIVE_COMPARATOR

carbamazepine ER

Intervention Type: DRUG

Active study drug, no comparator

Interventions

carbamazepine ER

Active study drug, no comparator

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age 19 -65.
• Diagnosis of Bipolar I or II Disorder, currently experiencing a major depressive episode without psychotic features, as confirmed by the Mini International Neuropsychiatric Interview (M.I.N.I.).
• Must have experienced at least two previous mood episodes during the past 10 years, at least one of which was a hypomanic, full manic or mixed episode. The current depressive episode must be ≥ 2 weeks, but ≤ 2 years in duration.
• Must currently have clinically significant depressive symptoms as defined by a CGI-S total score of ≥ 4.
• Must have been washed out of all psychotropic medications (except for the allowed concomitant sedatives for insomnia) for their bipolar illness for at least 3 days for mood stabilizers and 1 week for antidepressants prior to study drug initiation (medications should be tapered at the investigator's discretion prior to washout), while continuing to meet entry criteria for depressive symptoms. Must be willing to discontinue all psychotropic medication (except for the allowed concomitant sedative for insomnia) during the study period.
• No substance abuse/dependence for the previous 4 weeks (except for nicotine/caffeine)
• Must give informed consent, and/or consent must be obtained from a legally acceptable representative (as required by IRB) prior to the initiation of any protocol required procedures.
• Must be able to understand the nature of the study, agree to comply with the prescribed dosage regiments, report for regularly scheduled office visits and communicate to study personnel about adverse events and concomitant medication.
• Women of childbearing potential (WOCBP) must use medically approved methods of birth control to avoid pregnancy throughout the study and for up to four weeks after completion of the study in such a manner that the risk of pregnancy is minimized. WOCBP must have a negative serum or urine pregnancy test within 72 hours prior to the start of the study.
• Male or female, any race or ethic origin

Exclusion Criteria

• Patients with current diagnosis of delirium, dementia, amnestic or other cognitive disorder; schizophrenia; borderline or antisocial personality disorder; or any other mental disorder that would interfere with efficacy or safety evaluations or compliance.
• WOCBP who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to four weeks after completion of the study. Acceptable methods include oral, injectable or implanted contraceptives, intrauterine devices or barrier methods such as condoms, diaphragm, and spermicides. Women who are pregnant or breast-feeding, or who plan to become pregnant during the study.
• Patients at significant risk of committing suicide or homicide based on history, mental status exam, or investigator's judgment.
• Patients receiving psychotherapy (individual, group, marriage, or family therapy) unless participation has been regular for at least 3 months prior to randomization.
• Patients with clinically significant thyroid pathology that would interfere with efficacy or safety evaluations and patients with a thyroid stimulating hormone (TSH) level > 60% above the upper limit of normal. Patients who are undergoing treatment for their thyroid pathology (e.g. thyroid supplementation) should be stable for at least two months prior to randomization.
• Patients who have a history or evidence of a medical condition that would expose them to an undue risk of a significant adverse event or interfere with assessments of safety or efficacy during the course of the trial, including but not limited to hepatic, renal respiratory, cardiovascular, endocrine, neurologic, or hematologic disease as determined by the clinical judgment of the investigator.
• Patients with a history of seizures (except for a single childhood febrile seizure, posttraumatic, alcohol withdrawal) or a history of severe head trauma, or stroke.
• Patients on medications that may have serious drug-drug interactions with ERC-CBZ
• Clinically significant abnormal laboratory tests results:

• Platelets < 75,000/mm³
• Hemoglobin < 9g/dL
• Neutrophils, Absolute < 1000/mm³
• SGOT (AST) >3x Upper limit of Normal
• SGPT (ALT) > 3x Upper Limit of Normal
• Creatinine >2mg/dL
• Diastolic blood pressure >105 mmHg
• TSH > 60% above Upper Limit of Normal
• Detectable levels of cocaine and amphetamines in the urine drug screen.
• Other abnormal laboratory test or vital sign result that in the investigator's judgment, is medically significant, in that it would impact the safety of the patient or the interpretation of the results.
• Patients who are known to be allergic or hypersensitivity to carbamazepine (or alternative formulations).
• Patients who have failed an adequate trial of carbamazepine (or alternative formulations) for bipolar depression.
• Patients who have had recent treatment with a long-acting antipsychotic in which the last dose was less than one full cycle plus one week
• Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or physical (e.g. infectious disease) illness during the study.

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shire

INDUSTRY

Sponsor Role: collaborator

Tuscaloosa Research & Education Advancement Corporation

OTHER

Sponsor Role: lead

Responsible Party

Tuscaloosa Research Education & Advancement Corporation

Principal Investigators

Lori L Davis, MD

Role: PRINCIPAL_INVESTIGATOR

Tuscaloosa Veterans Affairs Medical Center

Locations

Tuscaloosa Research and Education Advancement Corporation

Tuscaloosa, Alabama, United States

Countries

United States

References

Swainston Harrison T, Keating GM. Extended-release carbamazepine capsules : in bipolar I disorder. CNS Drugs. 2005;19(8):709-16. doi: 10.2165/00023210-200519080-00006.

Reference Type: BACKGROUND

PMID: 16097852 (View on PubMed)

Other Identifiers

TREAC Equetro in Bipolar

Identifier Type: -

Identifier Source: secondary_id

TREAC Equetro in Bipolar

Identifier Type: -

Identifier Source: org_study_id