The main purpose of this observational study with Paclitaxel is to determine the number of treatment cycles and the quantity of Paclitaxel onkovis needed therefore under the special circumstance of ambulant chemotherapy. onkovis aims an economical utilization of the chemotherapeutics.The provision with adapted packaging sizes as to decrease the excess quantity to be discarded follows also this objective. Secondary objectives are the survey of the side effects of Paclitaxel onkovis in comparison to Docetaxel. To this purpose, data regarding co medications and adverse events are also collected.
Study Type
OBSERVATIONAL
Enrollment
770
Practice
Brandenburg, Germany
Practice
Chemnitz, Germany
Practice
Dresden, Germany
Practice
Mühlhausen, Germany
Practice
Plauen, Germany
the quantity of Paclitaxel onkovis needed pro treatment cycle
Determine the quantity of Paclitaxel onkovis needed pro treatment cycle
Time frame: the time the participants will be followed depends on the number of treatment cycles; that means the time frame may extend up to 24 weeks (8 cycles).
adverse events during and after treatment in comparison to Docetaxel onkovis
The number and kind of adverse events during and after the intra-venous application of Paclitaxel will be assessed, documented and compared to those of Docetaxel.
Time frame: up to 24 weeks (8 cycles)
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