CPK dosage
BiologicalCPK dosage during a blood sample realized at least one week after the begining of the treatment
NCT Number: NCT01248429
This study describes the elevation of CPK in patient treated for solid tumors by TKI
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Notify Me18 year and older
All sexes
Observational
Centre Paul Papin, Angers, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
CPK dosage during a blood sample realized at least one week after the begining of the treatment
Examination of the patient for myalgia, cramps, medical history and concomitant medication
Time frame: Within 3 days after a clinical exam
Dosage of CPK during standard blood sampling. The increase of CPK is defined when CPK value > USL
Time frame: During the clinical exam
To determine the correlation between myalgia and CPK blood, taking into account the risk factors leading to CPK increase
Centre Oscar Lambret
Other
National Study of Prevalence of Creatinine Phosphokinase (CPK) Increase in Patients With Solid Tumors Treated by Inhibitors of Tyrosine Kinases (TKI)
Acronym: TKI-CPK
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