Celsius TCS Hyperthermia System PMCF Trial

Celsius42

Status: Withdrawn

Conditions: Solid Neoplasms

Treatments: Device: Hyperthermia

Study type: Observational

Funder types: Industry

Identifiers

NCT02896049

TD08-200

Details and patient eligibility

About

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.

Full 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.

Sex: All

Ages: 18 to 99 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• treatment performed with the Celsius TCS Hyperthermia System

Exclusion criteria

• not applicable -

Trial design

0 participants in 1 patient group

Hyperthermia

Description:

treatment with the Celsius42 Hyperthermia System

Treatment:

Device: Hyperthermia