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A Study of T3 Therapy in Patients With Hypothyroidism

Primary Purpose

Hypothyroidism

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Liothyronine, Sodium
Sponsored by
Ipe, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypothyroidism

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Hypothyroid patients taking levothyroxine
  • Age 18-65
  • Able to make weekly in-person visits to Washington, D.C.

Exclusion Criteria:

  • Pregnancy or lactation
  • Chronic medical conditions such as heart disease or any other chronic medical conditions such as lung disease (e.g. asthma), kidney disease (e.g. kidney failure), liver disease (e.g. hepatitis), diabetes, or cancer.
  • Steroid medications such as estrogen, progesterone, estrogen or progesterone related medications, testosterone, or glucocorticoids
  • Already taking T3

Sites / Locations

  • Georgetown University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Liothyronine, Sodium

Arm Description

Outcomes

Primary Outcome Measures

Measurement of Blood Levels of Thyroid Hormone Sensitive Parameters
Serum Total T3, TSH

Secondary Outcome Measures

Measurement of Oxygen Consumption
Resting Metabolic Rate

Full Information

First Posted
February 18, 2013
Last Updated
July 1, 2014
Sponsor
Ipe, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT01800617
Brief Title
A Study of T3 Therapy in Patients With Hypothyroidism
Official Title
Phase II Single Daily-Dose Response Study of a New Liothyronine Sodium (T3) Preparation With Sustained Effects in Hypothyroid Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ipe, LLC

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test a new thyroid hormone preparation. The thyroid gland produces two thyroid hormones: mostly T4 and a smaller amount of T3. Thyroid hormone therapy for hypothyroidism or thyroid cancer is generally provided using levothyroxine, which is a synthetic form of T4. T4 is converted into the active hormone T3 in the circulation. Therefore, some researchers believe that T3 levels in T4-treated patients may be slightly lower than in individuals whose own thyroid gland is functioning normally. Symptoms of hypothyroidism have been suggested to occur because of this possible T3 deficiency, although this is controversial. Studies of T3, added to or substituted for T4 in traditional levothyroxine regimens, have generally not shown any benefit of T3. However, it is still possible that no benefit is seen because of the short duration of action or "half-life" of T3. This short-life makes it necessary to dose T3 twice or three times daily. Despite multiple daily doses of T3, T3 levels during its therapy tend to be troubled by peaks and troughs. These peaks can be associated with symptoms of excessive thyroid hormone levels. This study will look at TSH and thyroid hormone levels following a daily dose of a new preparation of T3 that may have longer duration of action than liothyronine. This preparation of T3 is called Thyromax® or BCT303. The investigators believe that steady levels of T3 will be seen after taking Thyromax®. The investigators believe that in patients with hypothyroidism use of Thyromax® in the correct dose will produce normal TSH levels, without producing symptoms of too much thyroid hormone. The goal of future studies is to test whether Thyromax® may be a potential treatment for hypothyroidism, by comparing it with traditional levothyroxine therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypothyroidism

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Liothyronine, Sodium
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Liothyronine, Sodium
Primary Outcome Measure Information:
Title
Measurement of Blood Levels of Thyroid Hormone Sensitive Parameters
Description
Serum Total T3, TSH
Time Frame
Six Weeks.
Secondary Outcome Measure Information:
Title
Measurement of Oxygen Consumption
Description
Resting Metabolic Rate
Time Frame
Six Weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hypothyroid patients taking levothyroxine Age 18-65 Able to make weekly in-person visits to Washington, D.C. Exclusion Criteria: Pregnancy or lactation Chronic medical conditions such as heart disease or any other chronic medical conditions such as lung disease (e.g. asthma), kidney disease (e.g. kidney failure), liver disease (e.g. hepatitis), diabetes, or cancer. Steroid medications such as estrogen, progesterone, estrogen or progesterone related medications, testosterone, or glucocorticoids Already taking T3
Facility Information:
Facility Name
Georgetown University Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States

12. IPD Sharing Statement

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A Study of T3 Therapy in Patients With Hypothyroidism

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