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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01758666
Other study ID # CIH-WAC-201205001
Secondary ID
Status Active, not recruiting
Phase N/A
First received August 30, 2012
Last updated December 21, 2015
Start date September 2012
Est. completion date December 2016

Study information

Verified date December 2012
Source Tianjin Medical University Cancer Institute and Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

At present, the most effective drugs to osteosarcoma include ADM,DDP,,HD-MTX,IFO and so on.The effective rate of single drug was about 30%, and if the chemotherapy contains HD-MTX, the survival rate can reach about 60%, so the HD-MTX is the most important component in patients of osteosarcoma.

Studies have shown that, MTX efficacy and adverse reactions were associated with blood concentration level and duration, selecting the right time and dose to give CF is the critical point.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date December 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender Both
Age group 12 Years to 60 Years
Eligibility Inclusion Criteria:

1. Proved by pathology in 60 cases of osteosarcoma patients

2. PS = 2, survival period is more than 6 months

3. Normal function of liver and kidney

4. No chemotherapy contraindication, patients treat with high dose methotrexate

5. Get signed written informed consent form

6. Have a good compliance with take blood and follow-up

Exclusion Criteria:

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Methotrexate,Calcium folinate


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tianjin Medical University Cancer Institute and Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary blood concentration of MTX up to 3 years Yes
Secondary other adverse reaction up to 3 years Yes
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