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Method of Endogenous TSH Stimulation in the Follow-up of Differentiated Thyroid Cancer

Primary Purpose

Thyroid Cancer

Status
Completed
Phase
Not Applicable
Locations
Estonia
Study Type
Interventional
Intervention
L-thyroxin
Sponsored by
University of Tartu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Thyroid Cancer focused on measuring thyroid cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Differentiated thyroid cancer
  • treated by thyroidectomy and at least 1 ablation with 131-I > 5 months ago
  • TSH < 4 imU/L

Exclusion Criteria:

  • Pregnancy
  • Known metastasis

Sites / Locations

  • East Tallinn Central Hospital
  • Tartu University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

L-thyroxin

Arm Description

this is one arm study

Outcomes

Primary Outcome Measures

TSH level at the end of study
The percentage of patients obtaining TSH level at least 30 imU/L at the end of study period. Blood tests will be obtained after 4 weeks. If TSH > 30 the patient has completed the study. If TSH < 30 patient will continue for 1 week and blood tests will be obtained after week 5. If TSH > 30 the patient has completed the study. If TSH < 30 patient will be monitored during 1 week and blood tests will be obtained after 6 weeks.

Secondary Outcome Measures

change in Billewitz index during the study
Billewitz index measures the severity of hypothyroidism symptoms. Billewitz index will be recorded after 4 weeks and after 5 and 6 weeks if patient continues after 4 or 5 weeks (see primary endpoint for details).

Full Information

First Posted
April 22, 2013
Last Updated
March 13, 2014
Sponsor
University of Tartu
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1. Study Identification

Unique Protocol Identification Number
NCT01840332
Brief Title
Method of Endogenous TSH Stimulation in the Follow-up of Differentiated Thyroid Cancer
Official Title
Method of Endogenous TSH Stimulation in the Follow-up of Differentiated Thyroid Cancer
Study Type
Interventional

2. Study Status

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

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Tartu

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The treatment of differentiated thyroid cancer (DCT) includes surgery followed by radioiodine treatment. In the follow-up of patients it is necessary to induce TSH elevation to test for cancer recurrence. One of the options is to stop L-thyroxin replacement for several weeks. Current pilot study aims to induce the necessary TSH elevation by decreasing the L-thyroxin dose. The main hypothesis is that necessary TSH stimulation will be achieved during 4-6 weeks in majority of patients.
Detailed Description
The treatment of differentiated thyroid cancer (DCT) includes surgery followed by radioiodine treatment. In the follow-up of patients it is necessary to induce TSH elevation for the measurement of thyreoglobulin and/or total body scanning. There are two principal methods to obtain TSH elevation: 1) injection of recombinant human TSH , and 2) to stop L-thyroxin replacement for several (3-4) weeks. As use of recombinant TSH is rather expensive, this method is not feasible in many countries. The problem with stopping L-thyroxin is development of severe hypothyroidism for several weeks with concomitant symptoms and signs. Current pilot study aims to induce the necessary TSH elevation by decreasing the L-thyroxin dose. The main hypothesis is that necessary TSH stimulation will be achieved during 4-6 weeks in majority of patients with fixed dose of L-thyroxin. Concomitantly, blood tests and symptoms and signs of hypothyroidism will be obtained to get information about possible deviations during treatment with low dose of thyroxin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid Cancer
Keywords
thyroid cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
L-thyroxin
Arm Type
Experimental
Arm Description
this is one arm study
Intervention Type
Drug
Intervention Name(s)
L-thyroxin
Intervention Description
Low dose of L-thyroxin (50 microg/day) will be used during 4 weeks. If TSH is < 30 after 4 weeks the study continues up to 6 weeks.
Primary Outcome Measure Information:
Title
TSH level at the end of study
Description
The percentage of patients obtaining TSH level at least 30 imU/L at the end of study period. Blood tests will be obtained after 4 weeks. If TSH > 30 the patient has completed the study. If TSH < 30 patient will continue for 1 week and blood tests will be obtained after week 5. If TSH > 30 the patient has completed the study. If TSH < 30 patient will be monitored during 1 week and blood tests will be obtained after 6 weeks.
Time Frame
4-6 weeks
Secondary Outcome Measure Information:
Title
change in Billewitz index during the study
Description
Billewitz index measures the severity of hypothyroidism symptoms. Billewitz index will be recorded after 4 weeks and after 5 and 6 weeks if patient continues after 4 or 5 weeks (see primary endpoint for details).
Time Frame
4-6 weeks
Other Pre-specified Outcome Measures:
Title
change in biochemical parameters during the study
Description
Change in parameters related to hypothyroidism (thyroid hormones, creatinine kinase, cholesterol,ultra sensitive CRP, creatinine).
Time Frame
4-6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Differentiated thyroid cancer treated by thyroidectomy and at least 1 ablation with 131-I > 5 months ago TSH < 4 imU/L Exclusion Criteria: Pregnancy Known metastasis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vallo Volke, MD, PhD
Organizational Affiliation
Tartu University
Official's Role
Principal Investigator
Facility Information:
Facility Name
East Tallinn Central Hospital
City
Tallinn
ZIP/Postal Code
10138
Country
Estonia
Facility Name
Tartu University Hospital
City
Tartu
ZIP/Postal Code
50406
Country
Estonia

12. IPD Sharing Statement

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Method of Endogenous TSH Stimulation in the Follow-up of Differentiated Thyroid Cancer

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