Efficacy of Sr-89 for Differentiated Thyroid Cancer With Bone Metastases

NCT ID: NCT05466812

Last Updated: 2022-07-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-13

Study Completion Date

2025-07-13

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Thyroid Neoplasm Follicular Bone Metastases

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Sr-89 treatment
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Sr-89 treated group

Sr-89 treatment

Group Type EXPERIMENTAL

Sr-89

Intervention Type DRUG

1. strontium-89 chloride treatment
2. periodical evaluation and follow-up

Interventions

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Sr-89

1. strontium-89 chloride treatment
2. periodical evaluation and follow-up

Intervention Type DRUG

Other Intervention Names

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strontium-89 chloride

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking Union Medical College Hospital

OTHER

Sponsor Role lead

Responsible Party

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Yansong Lin

Vice director

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yan-Song Lin

Role: PRINCIPAL_INVESTIGATOR

Peking Union Medical College Hospital

Locations

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Peking Union Medical College Hospital

Beijing, , China

Site Status

Countries

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China

Central Contacts

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Yan-Song Lin

Role: CONTACT

861069155610

Xian-Feng Cao

Role: CONTACT

861069156874

Facility Contacts

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Yan-Song Lin

Role: primary

Other Identifiers

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ZS-3477

Identifier Type: -

Identifier Source: org_study_id

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