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Celsius TCS Hyperthermia System PMCF Trial

2016-09-12 18:38:22 | BioPortfolio

Summary

Based on the basic data of all patients foreseen for a local hyperthermia in the participating centers the failure rate (of the Celsius TCS Hyperthermia System) and the complication rate (injury to the patients) will be recorded.

Description

During this PMCF Trial from each participating center the internal data of all Celsius TCS Hyperthermia devices are collected. The participating centers are obligated to report any device-related failure and Adverse Event (injury to the patient). The center reports together with the device-internal data allows to calculate the failure and the complication rates. It will be analyzed regarding the kind of tumor and the concomitant treatment (radiotherapy and/or chemotherapy). The outcome groups (with/without failure or complication) will be analyzed regarding demographic and treatment parameters.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Conditions

Solid Neoplasms

Intervention

Hyperthermia

Status

Not yet recruiting

Source

Celsius42 GmbH

Results (where available)

View Results

Links

Published on BioPortfolio: 2016-09-12T18:38:22-0400

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