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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03932058
Other study ID # PR-OS-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date September 1, 2020

Study information

Verified date April 2019
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact zhan Wang, Dr.
Phone +8618758586092
Email wangzhan515@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospectively collected 400 cases of clinical data and pathological paraffin specimens of osteosarcoma, chondrosarcoma (control) and endogenous chondroma (control) in our hospital from 2008 to 2014, combined with high-pressure cycle-satellite scanning mass spectrometry (PCT-SWATH) Molecular typing of osteosarcoma and prediction of targeted therapy, the establishment of a new molecular classification based on proteomics for osteosarcoma to predict the chemotherapy response and recurrence risk of osteosarcoma. Clinical osteosarcoma patients include as many types as possible: pre-chemotherapy, post-chemotherapy, recurrence, and metastasis. The study did not involve vulnerable groups, and it was taken as a postoperative wax specimen for patients, which had no health, life and other effects on patients. Study application exemption from informed consent.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date September 1, 2020
Est. primary completion date September 1, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- all osteosarcoma patients in our hospital

- received Methotrexate+Doxorubicin+Cisplatin protocol chemotherapy

Exclusion Criteria:

- non-chemotherapy patients

- bio-specimen not completed

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Chemotherapy
all osteosarcoma patients will give regular chemotherapy for osteosarcoma, the protocol is the same as Methotrexate+Doxorubicin+Cisplatin.

Locations

Country Name City State
China 2nd Affiliated Hospital of Zhejiang University Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary proteomics changes Study of changes in proteomes in tumor cells by high-throughput proteomics analysis 2 years
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