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Phase 4 Study in Secondary Hypothyroidism: Body Weight Adapted Thyroxin Treatment and Triiodothyronine Supplementation

Primary Purpose

Secondary Hypothyroidism, Hypopituitarism, Hyperlipidemias

Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Thyroxin, Triiodothyronine
Sponsored by
University Hospital Freiburg
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Secondary Hypothyroidism focused on measuring secondary hypothyroidism, body weight adjusted thyroxin dose, triiodothyronine supplementation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: hypopituitarism of at least 3 axes (TSH plus gonadotropin, somatotropin, corticotropin or ADH deficiency) termination of surgical or radiation treatment of pituitary tumors at least six month before study entry BMI of 20 - 39.9 kg/m2 non-smoking status. Exclusion Criteria: history of cardiovascular or pulmonary diseases current thyroxin dosage > 1.6 µg/kg bw pregnancy epilepsy cerebrovascular diseases nodular goiter

Sites / Locations

  • University Hospital Freiburg, Department of Medicine

Outcomes

Primary Outcome Measures

well-being
cognitive function

Secondary Outcome Measures

lipid metabolism
muscle function / ankle reflex time

Full Information

First Posted
August 2, 2006
Last Updated
June 6, 2008
Sponsor
University Hospital Freiburg
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1. Study Identification

Unique Protocol Identification Number
NCT00360074
Brief Title
Phase 4 Study in Secondary Hypothyroidism: Body Weight Adapted Thyroxin Treatment and Triiodothyronine Supplementation
Official Title
A Randomised, Controlled, Crossover Study: Treatment With Thyroxin Compared to Thyroxin + Triiodothyronin in Patients With Secondary Hypothyroidism
Study Type
Interventional

2. Study Status

Record Verification Date
June 2008
Overall Recruitment Status
Completed
Study Start Date
February 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Freiburg

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine whether a body weight adjusted dose of thyroxin is superior to treatment guided by laboratory results of thyroxin hormones in patients with central hypothyroidism. Moreover beneficial effects of triiodthyronine supplementation are investigated.
Detailed Description
Backround: A normal thyroid function is critical for metabolism, well-being and cognitive function. It is now well accepted that primary subclinical hypothyroidism, characterized by normal circulating thyroid hormones (fT3 and fT4) and elevated TSH, should be treated to improve reduced quality of life and abnormalities of lipid metabolism. In central hypothyroidism (CH) the dose of replacement therapy aims to achieve normal thyroxin (T4) concentrations as defined by appropriate reference populations. Adequate thyroxin treatment is especially challenging, as T4 cannot be titrated according to endogenous TSH levels because of the impaired hypothalamic-pituitary unit. The majority of untreated CH patients show normal (40 %) or elevated TSH levels (35 %) while only a minority has reduced concentrations (25 %) {Faglia, 1979 #1}. These findings are explained by the lack of pulsatile secretion and nocturnal TSH surge, which has been attributed to impaired thyrotroph function in CH patients {Caron, 1986 #2}. Moreover, impaired biological activity of TSH itself due to reduced glycosylation has been described in secondary hypothyroidism. In a cross sectional study performed in patients with central hypothyroidism, we found elevated cholesterol levels and increased ankle reflex time suggesting subtle hypothyroidism, though fT3 and fT4 serum concentrations were within the normal range. The average dose of thyroxin (T4) applied in these patients with central hypothyroidism was 1.1 µg/kg bw, which is below the average dose recommended in primary hypothyroidism (1.6 µg/kg bw). We hypothesized that these results might indicate suboptimal T4 replacement therapy, not detectable by current laboratory testing. Hypothesis: To investigate the effects of a body weight adjusted T4 or T3T4 dose on metabolism, well-being and cognitive function. Study design: Placebo controlled trial in patients with central hypothyroidism following a double blind cross-over design. Intervention: Three different treatment regimes (5 weeks each) were compared: "CON-T4", empirically chosen, current dose of T4 (1 ± 0.05 μg/kg body weight (bw); "OPT-T4", optimized T4 treatment (1.6 μg/kg bw T4); "T3T4", combination of triiodothyronine (T3, 0.16) and T4 (1.44 μg/kg bw). Biochemical parameters, ankle reflex time and neurocognitive functions were assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Secondary Hypothyroidism, Hypopituitarism, Hyperlipidemias
Keywords
secondary hypothyroidism, body weight adjusted thyroxin dose, triiodothyronine supplementation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
25 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Thyroxin, Triiodothyronine
Primary Outcome Measure Information:
Title
well-being
Time Frame
3 weeks of treatment
Title
cognitive function
Time Frame
3 weeks of treatment
Secondary Outcome Measure Information:
Title
lipid metabolism
Time Frame
3 weeks of treatment
Title
muscle function / ankle reflex time
Time Frame
3 weeks of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: hypopituitarism of at least 3 axes (TSH plus gonadotropin, somatotropin, corticotropin or ADH deficiency) termination of surgical or radiation treatment of pituitary tumors at least six month before study entry BMI of 20 - 39.9 kg/m2 non-smoking status. Exclusion Criteria: history of cardiovascular or pulmonary diseases current thyroxin dosage > 1.6 µg/kg bw pregnancy epilepsy cerebrovascular diseases nodular goiter
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prof Dr Martin Reincke, MD
Organizational Affiliation
former Medical Professor of University Hospital Freiburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Freiburg, Department of Medicine
City
Freiburg
State/Province
Baden-Württemberg
ZIP/Postal Code
79104
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
17711927
Citation
Slawik M, Klawitter B, Meiser E, Schories M, Zwermann O, Borm K, Peper M, Lubrich B, Hug MJ, Nauck M, Olschewski M, Beuschlein F, Reincke M. Thyroid hormone replacement for central hypothyroidism: a randomized controlled trial comparing two doses of thyroxine (T4) with a combination of T4 and triiodothyronine. J Clin Endocrinol Metab. 2007 Nov;92(11):4115-22. doi: 10.1210/jc.2007-0297. Epub 2007 Aug 21.
Results Reference
result

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Phase 4 Study in Secondary Hypothyroidism: Body Weight Adapted Thyroxin Treatment and Triiodothyronine Supplementation

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