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Heat Treatment With Radiation for Advanced Cervical Cancer

Tests heat therapy added to radiation and internal radiation in women with advanced cervical cancer.

Plain-language title generated from the registry record
Registry title: Radiation Therapy or Chemoradiation, Interstitial Brachytherapy in Combination With Hyperthermia in Advanced Cervical Cancer

Key facts

Where
Erlangen, GermanySee the site

Where in Germany

  • Universitätsklinikum Erlangen, StrahlenklinikErlangen, GermanyTaking people

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Trial details

Who runs it
University of Erlangen-Nürnberg Medical School
Trial code
NCT03249519
Record updated
15 August 2017
Original description
The combination of radiation therapy or chemoradiation with Interstitial brachytherapy for advanced cervical cancer (pN+, FIGO-Stage II B - IV A is standard of therapy. The radio- and chemosensitive effect of an additional hyperthermia might improve the clinical outcome.Read full original descriptionShow less

Multimodal Therapy of Advanced Cervical Cancer With Radiotherapy or Chemoradiation, Interstitial Brachytherapy in Combination With Hyperthermia

The combination of radiation therapy or chemoradiation with Interstitial brachytherapy for advanced cervical cancer (pN+, FIGO-Stage II B - IV A is standard of therapy. The radio- and chemosensitive effect of an additional hyperthermia might improve the clinical outcome.

Inclusion: Histological confirmed carcinoma of the Cervix; FIGO-Stage IIB-IVA; earlier stages when inoperable or according to patient's wish; clinical M0; except: involvement of para-aortic lymph nodes; Age ≥ 18 years; ECOG ≤ 2; Informed consent of the patient.

Exclusion: Metal implants (length > 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 chemoradiation or deep regional hyperthermia; Active or therapy-resistent bladder infections; Pre-existing or concommitant immunodeficiency Syndrome; Complete bundle branch block; Pregnant or lactating women.

ClinicalTrials.gov NCT03249519