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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00525122
Other study ID # 2006/60
Secondary ID
Status Recruiting
Phase N/A
First received September 4, 2007
Last updated May 21, 2008
Start date September 2007

Study information

Verified date May 2008
Source Medisch Centrum Rijnmond-Zuid, Netherlands
Contact A. Berghout, MD, PhD
Phone 0031 10 2913368
Email BerghoutA@mcrz.nl
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Observational

Clinical Trial Summary

Hypothesis: What is the natural course after treatment with radioactive iodine in patients with hyperthyroidism?

What are the determinants for the development of acute hypo- or hyperthyroidism after treatment with radioactive iodine without antithyroid drugs?


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients wth hyperthyroidism who are eligible for treatment with radioactive iodine

- Age > 18 years

Exclusion Criteria:

- Severe ophthalmopathy

- Pregnancy or wish to pregnancy on short term

- Breastfeeding

- Patients already treated with radioactive iodine

- Known cardiovascular diseases or other severe comorbidity

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Netherlands MCRZ Rotterdam Zuid-Holland

Sponsors (1)

Lead Sponsor Collaborator
Medisch Centrum Rijnmond-Zuid, Netherlands

Country where clinical trial is conducted

Netherlands, 

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