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Taking people in GermanyNo phase

Heat Therapy With Radiation or Chemoradiation for Bladder Cancer

Tests heat treatment added to radiation or chemoradiation in adults with bladder cancer.

Plain-language title generated from the registry record
Registry title: Organ-preservative Therapy of Bladder Cancer With Radiotherapy or Radiochemotherapy Combined With Hyperthermia

Key facts

Where
Erlangen, GermanySee the site

Where in Germany

  • Dept. of Radiation Therapy, University Hospital ErlangenErlangen, GermanyTaking people

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
University of Erlangen-Nürnberg Medical School
Trial code
NCT05397262
Record updated
9 May 2024
Original description
Analysis of the efficacy and the compatibility of deep regional hyperthermia in combination with radiotherapy and chemoradiotherapy in bladder cancerRead full original descriptionShow less

Register-Trial Based on an Agreement of Health Insurances With the Department of Radiation Therapy of the University Hospital Erlangen for the Application of Regional Hyperthermia in Bladder Cancer: Organ-preservative Therapy of Bladder Cancer With Radiotherapy or Radiochemotherapy Combined With Hyperthermia

Analysis of the efficacy and the compatibility of deep regional hyperthermia in combination with radiotherapy and chemoradiotherapy in bladder cancer

Inclusion: Age ≥ 18 years; Histologically confirmed bladder cancer; M0; ECOG-performance status ≤ 2; Informed consent.

Exclusion: Metal implants (lenght > 2cm or dense clusters of marker clips in the pelvis); Patients not willing to use effective contraception during and up to 6 months after therapy; Pre-existing uncontrolled cardiac disease, signs of cardiac failure, or rhythm disturbances requiring therapy; Cardiac Pacemaker; Myocardial infarction within the past 12 months; Congestive heart failure; New York Heart Association (NYHA) class III or IV heart disease; Disease that would preclude TUR, chemoradiation or deep regional hyperthermia; Active or therapy-resistent bladder infections; Complete bundle branch block; Pre-existing or concommitant immunodeficiency Syndrom; Pregnant or lactating women.

ClinicalTrials.gov NCT05397262