Does Radioiodine Treatment Prevent Atrial Fibrillation and Bone Loss in Endogenous Subclinical Hyperthyroidism?

Sponsor
Radboud University Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT00151723
Collaborator
(none)
200
5
40

Study Details

Study Description

Brief Summary

Subclinical hyperthyroidism is defined as the presence of serum free thyroxine (T4) and triiodothyronine (T3) levels within the reference range and a reduced serum thyrotrophin (TSH) level. Evidence is accumulating that it has important clinical effects. The SUBstudy is a randomised, Dutch multicenter trial to study whether radioiodine treatment prevents the development of atrial fibrillation and prevents decreases in bone mineral density in patients with endogenous subclinical hyperthyroidism.

Condition or Disease Intervention/Treatment Phase
  • Procedure: treatment with 131I
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Subclinical Hyperthyroidism "To Treat or Not to Treat?" A Dutch Multicenter Trial
Study Start Date :
Apr 1, 2004

Outcome Measures

Primary Outcome Measures

  1. To provide evidence that restoration of euthyroidism (normal TSH) improves thyrotoxic symptoms and signs and quality of life and lowers the risk of subsequent atrial fibrillation and bone loss in subjects with endogenous subclinical hyperthyroidism []

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subclinical hyperthyroidism [TSH ≤ 0.1 mU/L, fT4 and T3 within the normal range of the own laboratory (determined 2 times in own laboratory) with an interval of at least 2 months].

  • Endogenous cause of subclinical hyperthyroidism limited to autonomous adenoma or multinodular goiter (diagnosis made by the attending physician, based on palpation and the result of a thyroid scintigram).

  • Informed consent.

Exclusion Criteria:
  • Medication with anti-thyroid drugs in the last 3 months (also not allowed during follow-up); thyroid hormone in the last 3 months (allowed during follow-up, but TSH levels should be kept between 0.1 mU/L and the upper limit of normal in the own laboratory); and oral glucocorticoids in the last 3 months (allowed during follow-up when absolutely necessary, but patients in whom glucocorticoids are started cannot be evaluated with respect to changes in bone mineral density [BMD]).

  • Radioiodine therapy in the past.

  • Iodine-induced subclinical hyperthyroidism.

  • Pituitary or hypothalamic insufficiency.

  • Pregnancy.

  • Age <= 40 years.

  • Severe non-thyroidal illness.

  • Drug abuse.

  • Unstable angina pectoris, (history of) atrial fibrillation, (history of) congestive heart failure.

  • (History of) osteoporotic fracture(s).

  • Patients younger than 70 years of age with a bone mineral density T-score < - 2.5 standard deviations (SD), or older than 70 years of age with a bone mineral density Z-score < 1.0 SD. (These patients can be randomized but in case it is decided to treat them with anti-osteoporotic drugs they cannot be evaluated with respect to changes in BMD.)

  • Use of betablockers in the last three months. (These patients can be randomised but cannot be evaluated with respect to general and cardiac symptoms. The same applies to patients in whom betablockers are started during follow up.)

  • Other symptoms or signs of hyperthyroidism or obstruction of vital structures which, in the opinion of the attending physician, require active treatment.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Academical Medical Centre Amsterdam Amsterdam Netherlands
2 Martini Ziekenhuis Groningen Groningen Netherlands
3 University Hospital Groningen Groningen Netherlands
4 Radboud University Medical Centre Nijmegen Nijmegen Netherlands 6500HB
5 Maxima Medisch Centrum Veldhoven Netherlands

Sponsors and Collaborators

  • Radboud University Medical Center

Investigators

  • Principal Investigator: Ad Hermus, MD, Prof, Radboud University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00151723
Other Study ID Numbers:
  • SUBstudie
First Posted:
Sep 9, 2005
Last Update Posted:
Jul 18, 2007
Last Verified:
Sep 1, 2005
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 18, 2007