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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05466812
Other study ID # ZS-3477
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date July 13, 2022
Est. completion date July 13, 2025

Study information

Verified date July 2022
Source Peking Union Medical College Hospital
Contact Yan-Song Lin
Phone 861069155610
Email linys@pumch.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Using sensitive markers (such as thyroglobulin, etc) to evaluate the efficacy of strontium-89 chloride (Sr-89) in differentiated thyroid cancer with bone metastases with an aim to breaking out of its palliation effect for bone pain.


Description:

Using biochemical markers (such as thyroglobulin), functional markers (such as change of tumor-background ratio on bone scan), etc to evaluate the efficacy of strontium-89 chloride (Sr-89) in differentiated thyroid cancer with bone metastases with an aim to breaking out of its palliation effect for bone pain.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date July 13, 2025
Est. primary completion date July 13, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients of differentiated thyroid cancer - Positive uptake by bone metastases on bone scan - Planing to have Sr-89 treatment Exclusion Criteria: - Having received treatment for bone metastases within one month of the study (such as radiotherapy, surgery, targeted therapy, chemotherapy, etc., among which denosumab and bisphosphate were allowed as basic treatment) - Having received radioactive iodine therapy within half a year before the study - There are bone related events, such as fracture, spinal cord compression, etc.

Study Design


Intervention

Drug:
Sr-89
strontium-89 chloride treatment periodical evaluation and follow-up

Locations

Country Name City State
China Peking Union Medical College Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of serum thyroglobulin (Tg) level Change of serum Tg level Through study completion, an average of 1 week in the first months and 1 month thereafter, up to 6 months
Primary Change of serum thyroglobulin antibody (TgAb) level Change of serum TgAb level Through study completion, an average of 1 week in the first months and 1 month thereafter, up to 6 months
Primary Change of serum calcium level Change of serum calcium level Through study completion, an average of 1 week in the first months and 1 month thereafter, up to 6 months
Primary Change of serum alkaline phosphatase (ALP) level Change of ALP level Through study completion, an average of 1 week in the first months and 1 month thereafter, up to 6 months
Primary Change of tumor-background ratio on bone scan Change from baseline tumor-background ratio on bone scan at 3 months and 6 months Baseline, 3 months and 6 months
Primary Change of standardized uptake value (SUV) on positron emission tomography/ computed tomography (PET/CT) Change from baseline SUV on PET/CT at 3 months and 6 months Baseline, 3 months and 6 months
Secondary Structural change on image Structural change on image at 3 months and 6 months Baseline, 3 months and 6 months
Secondary Numerical rating scale (NRS) for pain Scale of 0 to 10, 0=no pain, 10=worst imaginable pain Through study completion, an average of 1 week in the first months and 1 month thereafter, up to 6 months
Secondary Skeletal related event (SRE) Any SRE such as pathological fractures, surgery/radiotherapy for pain/prevention of fractures, hypercalcemia, and spinal cord compression. Up to 6 months
Secondary Analgesics Quantification of the use of analgesics and changes over time Up to 6 months
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