Ignite Creation Date:
2024-05-05 @ 11:08 AM
Last Modification Date:
2024-10-26 @ 9:02 AM
Study NCT ID:
NCT00001730
Status:
COMPLETED
Last Update Posted:
2008-03-04
First Post:
1999-11-03
Brief Title:
Study of Radioiodine 131-I Uptake Following Administration of Thyrogen and Hypothyroid States During Thyroid Hormone Withdrawal
Sponsor:
National Institute of Diabetes and Digestive and Kidney Diseases NIDDK
Organization:
National Institutes of Health Clinical Center CC
Study Overview
Official Title:
A Dosimetry Study of Radioiodine 131-I Uptake Following the Administration of Thyrogen and Hypothyroid States During Thyroid Hormone Withdrawal
Status:
COMPLETED
Status Verified Date:
1999-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Thyroid cancer is typically treated with surgery radiation or a combination of both Following surgical removal of thyroid tissue patients receive thyroid hormone replacement medication In addition patients undergo tests to determine the status of the disease One of the tests conducted is a whole body scan using radioactive iodine to detect and locate any remaining cancerous thyroid tissue
Thyroid tissue uses iodine to make thyroid hormones T3 and T4 In order for a radioiodine scan to work cancerous thyroid tissue must be hungry for iodine Thyroid stimulating hormone TSH produced in the pituitary gland is responsible for making thyroid tissue hungry for iodine Once thyroid tissue absorbs the radioactive iodine it will be clearly visible on the scan and can be located for removal However thyroid hormone replacement medication tends to lower the activity of the pituitary gland and the amount of naturally produced TSH So it is necessary to stop thyroid hormone replacement to increase TSH A problem arises when there is a lack of thyroid hormone replacement causing patients to experience hypothyroidism This condition is associated with unpleasant physical and emotional symptoms
TSH has been created in a laboratory and called Thyrogen It is basically the same as the TSH produced in the human pituitary gland However Thyrogen increases the level of TSH in the body without having to stop thyroid replacement medication Therefore patients will not experience hypothyroidism while preparing for a radioactive iodine scan
The objective of this study is to compare the activity of radioiodine 131I in patients taking Thyrogen with normal thyroid activity versus patients with hypothyroid activity after thyroid replacement medication is withdrawn In addition the study will provide information on how radioactive iodine is eliminated from the body The study will help researchers understand how to give Thyrogen and radioiodine for purposes of scanning and therapeutic ablation the destruction of function of cancerous thyroid tissue
The study will accept patients with non-medullary thyroid cancer who are preparing for ablation therapy The patients will be placed in one of two groups Group one will receive Thyrogen in 2 doses 24 hours apart Group two will receive Thyrogen in 3 doses 72 hours apart The patients will undergo two 131I whole body scans one after Thyrogen while taking thyroid hormone suppressive and the second after withdrawal from thyroid hormone 131I ablative therapy will be given under hypothyroid conditions at the completion of the study
Thyroid tissue uses iodine to make thyroid hormones T3 and T4 In order for a radioiodine scan to work cancerous thyroid tissue must be hungry for iodine Thyroid stimulating hormone TSH produced in the pituitary gland is responsible for making thyroid tissue hungry for iodine Once thyroid tissue absorbs the radioactive iodine it will be clearly visible on the scan and can be located for removal However thyroid hormone replacement medication tends to lower the activity of the pituitary gland and the amount of naturally produced TSH So it is necessary to stop thyroid hormone replacement to increase TSH A problem arises when there is a lack of thyroid hormone replacement causing patients to experience hypothyroidism This condition is associated with unpleasant physical and emotional symptoms
TSH has been created in a laboratory and called Thyrogen It is basically the same as the TSH produced in the human pituitary gland However Thyrogen increases the level of TSH in the body without having to stop thyroid replacement medication Therefore patients will not experience hypothyroidism while preparing for a radioactive iodine scan
The objective of this study is to compare the activity of radioiodine 131I in patients taking Thyrogen with normal thyroid activity versus patients with hypothyroid activity after thyroid replacement medication is withdrawn In addition the study will provide information on how radioactive iodine is eliminated from the body The study will help researchers understand how to give Thyrogen and radioiodine for purposes of scanning and therapeutic ablation the destruction of function of cancerous thyroid tissue
The study will accept patients with non-medullary thyroid cancer who are preparing for ablation therapy The patients will be placed in one of two groups Group one will receive Thyrogen in 2 doses 24 hours apart Group two will receive Thyrogen in 3 doses 72 hours apart The patients will undergo two 131I whole body scans one after Thyrogen while taking thyroid hormone suppressive and the second after withdrawal from thyroid hormone 131I ablative therapy will be given under hypothyroid conditions at the completion of the study
Detailed Description:
This is a multi-centered open-labeled randomized two parallel-arm study designed to compare quantitative radiation dosimetry assessments obtained during thyroid hormone suppression therapy with recombinant human TSH Thyrogen Registered Trademark and hypothyroidism in thyroid cancer patients preparing for post-surgical radioiodine ablation The primary endpoint of this study is to identify the ratio of administered activity of radioiodine 131I to deliver a targeted dose of 30000 rad to the thyroid remnant when patients are euthyroid on Thyrogen Registered Trademark and hypothyroid after hormone withdrawal Secondary endpoints are to identify and compare effective 131I clearance and cumulated activity in the whole body and blood during euthyroid and hypothyroid states
All adult patients with differentiated non-medullary thyroid cancer who are preparing for ablation therapy are eligible for participation Patients will be randomized to one of two different dosing regimens of Thyrogen Registered Trademark Participants will undergo two 131I whole body scans one after Thyrogen Registered Trademark while taking thyroid hormone suppressive therapy and the second after withdrawal from thyroid hormone 131I ablative therapy will be given under hypothyroid conditions at the completion of the dosimetry study
All adult patients with differentiated non-medullary thyroid cancer who are preparing for ablation therapy are eligible for participation Patients will be randomized to one of two different dosing regimens of Thyrogen Registered Trademark Participants will undergo two 131I whole body scans one after Thyrogen Registered Trademark while taking thyroid hormone suppressive therapy and the second after withdrawal from thyroid hormone 131I ablative therapy will be given under hypothyroid conditions at the completion of the dosimetry study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 98-DK-0038 | None | None | None |