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Completed

NCT Number: NCT00790738

Liothyronine (T3) for Bipolar Depression

This study evaluates the efficacy of the thyroid hormone T3 for depression in patients with bipolar disorder. In this study patients will be randomized to receive T3 or placebo.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

The Zucker Hillside Hospital

Glen Oaks, New York, 11004, United States

About this study

Bipolar affective disorder is a debilitating illness, and is characterized by depression episodes that dominates the longitudinal course and are most difficult to treat. Controlled trials with monotherapy mood stabilizers such as lithium and valproate show little to no efficacy and antidepressants may offer no additional efficacy. Recently there has been a growing interest in the use of quetiapine in bipolar depression. However, a successful treatment may take up to 8 weeks, and full remission is achieved in only 50% of patients. Thyroid hormone augmentation strategies have been used in unipolar depression with good results, but there is a paucity of its efficacy in bipolar depression (BD). To our knowledge there are no controlled studies regarding the efficacy of thyroid augmentation in BD. The present study proposes to evaluate the efficacy of T3 as an augmentation to treatment as usual in the treatment of BD. We plan to enroll patients with bipolar disorder I or II who are currently presenting with depressive symptoms. Patients will be randomized to 2 groups - liothyronine or placebo Results will provide information on the possible role of thyroid hormone augmentation in the treatment of patients with bipolar depression, and may contribute to alleviate the burden of this disabling condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-65;
  • DSM-IV diagnosis of BP I or BP II as per SCID;
  • Currently presenting with at least moderate levels of depression (HAM-D > 15;
  • Patient has to be on stable dose of at least one mood stabilizer (lithium, valproate, carbamazepine, lamotrigine, second generation antipsychotics) for at least 4 weeks as per history;
  • Antidepressants and/or additional mood stabilizers are allowed, but dose should be stable for at least 2 weeks;

Exclusion criteria

  • Evidence of acute mania or hypomania (as measured by CARS-M > 7);
  • Abnormal (outside of lab normal range) thyroid function tests;
  • Current thyroid hormone treatment;
  • Any medical condition considered a contraindication for treatment with T3 (i.e. history of myocardial infarction, cardiac arrhythmia, severe cardiac insufficiency, Autoimmune Thyroid Disease /Hashimoto's Thyroiditis as determined by anti-thyroid antibody testing, previous or current thyroid adenoma, hyperthyroidism);
  • EKG showing rhythm other than sinus or repolarization phase abnormalities;
  • Current alcohol or substance abuse or dependence in past month as per SCID;
  • Score of 3 or more on the suicide item of the HAM-D;
  • Females who are pregnant, breastfeeding, or of childbearing age and not using adequate birth control.

Treatment and study plan

Liothyronine (T3)

Drug

liothyronine (T3) up to 50 micrograms a day

Other names: cytomel (liothyronine)

Placebo

Drug

placebo

Primary outcomes

  1. Hamilton Rating Scale for Depression Scores

    Time frame: 8 weeks

    The Hamilton Rating Scale for Depression (HRSD) is a checklist of items ranked from 0-4 or 0-2, that was designed to measure the severity of depressive symptoms. The scale ranges from 0 to 50, and the following thresholds are used: very severe >23, severe 19-22, moderate 14-18, mild 8-13 and normal ≤7.

Secondary outcomes

  1. Clinician-Administered Rating Scale for Mania

    Time frame: 8 weeks

    The Clinician-Administered Rating Scale for Mania (CARS-M) contains 15 items rated from 0-5 or 0-6 on a Likert scale. It was developed to assess severity of manic symtoms. The scale ranges from 0 to 50, and the following thresholds are used: severe ≥26, moderate 16-25, mild 8-15 and normal ≤7.

  2. Clinical Global Impression Scores

    Time frame: 8 weeks

    The Clinical Global Impression - Severity scale (CGI-S) is a 7-point scale that requires the clinician to rate the severity of the patient's illness at the time of assessment, relative to the clinician's past experience with patients who have the same diagnosis. At the time of rating patients are rated as: 1, normal, not at all ill; 2, borderline mentally ill; 3, mildly ill; 4, moderately ill; 5, markedly ill; 6, severely ill; or 7, extremely ill.

Sponsors and collaborators

Lead sponsor

Northwell Health

Other

Collaborators

  • National Alliance for Research on Schizophrenia and Depression

Registry information

Official study title

Randomized Double-Blind Trial of Liothyronine (T3) Augmentation to Treatment as Usual vs Placebo For The Treatment of Bipolar Depression

Acronym: T3

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Nov 13, 2008
Registry last updated
Jul 2, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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