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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02773667
Other study ID # I-131-07/2015
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date December 2022

Study information

Verified date December 2022
Source Jena University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Correlation analysis between estimated renal function and biological half life of 131-I during radioiodine treatment of patients with differentiated thyroid cancer.


Description:

131-I during radioiodine treatment of patients with differentiated thyroid cancer is mainly renally excreted. It is advised in the clinical guidelines that serum creatinine should be determined before applying 131-I and if necessary the administered dose should be reduced. Nevertheless no guideline gives advice in what extent the dose should be decreased. The adjustment is at the discretion of the attending physician. Aim of this prospective study is to correlate the biological half life of 131-I with the renal function to give objective recommendations concerning the reduction of the applied dose in patients with limited renal function.


Recruitment information / eligibility

Status Completed
Enrollment 83
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients with differentiated thyroid carcinoma - stationary for treatment or diagnostic with radioiodine - state after thyroidectomy - written consent of the patient - minimum age 18 years Exclusion Criteria: - no written consent of the patient - patients with large residual thyroid tissue (iodine uptake > 10%) - children under 18 years of age - inclusion in concurrent interventional studies - patients without TSH-stimulation by rhTSH

Study Design


Locations

Country Name City State
Germany University Hospital Jena Jena Thüringen

Sponsors (1)

Lead Sponsor Collaborator
Jena University Hospital

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between estimated renal function and biological half life of 131-I The estimated renal function (estimated GFR) is measured via determination of serum creatinine and Cystatin C.
The biological half-life of I-131 is determined via whole-body dosimetry (whole-body probe and whole-body gamma camera) and blood probe measurement.
Update 2017/06/07: After analyzing the preliminary results (based on the first 48 patients) probe measurements are not longer needed in a simplified study design. Additionally, measuring the creatinine concentration is no longer needed in comparison to the Cystatin C measurements.
2 years
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