- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Hyperthermia.
Displaying page 1 of 2.
EudraCT Number: 2007-003232-35 | Sponsor Protocol Number: 197-2004 | Start Date*: 2007-08-17 | |||||||||||
Sponsor Name:Medizin Universität Wien | |||||||||||||
Full Title: Dantrolen as treatment for hyperthermia in patients with subarachnoidal hemorrhage | |||||||||||||
Medical condition: Fever episodes occur in more than 50%of patients with subarachnoidal hemorrhage despite antibiotic and antipyretic therapy.The exact mechanism of hyperthermia-induced brain injury is not known. Hyp... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005862-36 | Sponsor Protocol Number: mammatherm | Start Date*: 2007-07-16 |
Sponsor Name:Klinikum der Universität München Innenstadt, I. Frauenklinik | ||
Full Title: Prospectively Randomized Phase I/II Trial of Liposomal-encapsulated Doxorubicin and Cisplatin +/- Locoregional Hyperthermia in patients with Metastatic Breast Cancer | ||
Medical condition: This is an open-label, multicenter, randomized controlled, Phase I/II study comparing the time to progressive disease after randomisation in patients treated with 6 cycles of liposomal-encapsulated... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000167-14 | Sponsor Protocol Number: 105-15-201 | Start Date*: 2017-02-16 | |||||||||||
Sponsor Name:CELSION CORPORATION | |||||||||||||
Full Title: HEAT-ACTIVATED TARGET THERAPY RADIOTHERAPY + HYPERTHERMIA + LYSO THERMOSENSITIVE LIPOSOMAL DOXORUBICIN) OF LOCALREGIONAL RELAPSE IN BREAST CANCER PATIENTS | |||||||||||||
Medical condition: Local-Regional Relapse in Breast Cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019225-33 | Sponsor Protocol Number: 31630 | Start Date*: 2010-05-18 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: A Randomized Phase II Study Of Reirradiation And Hyperthermia Versus Reirradiation And Hyperthermia Plus Chemotherapy For Locally Recurrent Breast Cancer In Previously Irradiated Area | |||||||||||||
Medical condition: All patients with a local regional recurrence of invasive breast cancer in previously irradiated area with measurable lesions not suitable for resection are eligible for this trial. Patients with m... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001419-25 | Sponsor Protocol Number: GastricCHIMERAtrial | Start Date*: 2021-04-09 | |||||||||||
Sponsor Name:Jagiellonian University Medical College | |||||||||||||
Full Title: Preoperative intraperitoneal chemotherapy in adjuvant hyperthermia adjunctive therapy in advanced gastric cancer with high-risk of peritoneal recurrence - a multicentre randomized trial | |||||||||||||
Medical condition: Gastric Carcinoma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004802-14 | Sponsor Protocol Number: HEAT | Start Date*: 2011-11-25 | ||||||||||||||||
Sponsor Name:Klinikum Grosshadern Medical Center, University of Munich | ||||||||||||||||||
Full Title: A randomized two-armed open study on the adjuvant therapy in patients with R0/R1 resected pancreatic carcinoma with Gemcitabine plus Capecitabine (Arm GC) vs. Gemcitabine plus Cisplatin with region... | ||||||||||||||||||
Medical condition: R0/R1 resected ductal pancreatic adenocarcinoma | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000224-17 | Sponsor Protocol Number: 11-36-14/12 | Start Date*: 2014-09-15 |
Sponsor Name:MAASTRO Clinic | ||
Full Title: Non invasive imaging of [18F]HX4 with Positron-Emission-Tomography (PET) in Cervix Cancer. | ||
Medical condition: Eligible patients with squamous cell carcinoma, adenocarcinoma or adenosquamous carcinoma (FIGO stage IB – IVA), to be treated with curative radiation treatment either or not combined with concurr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000736-25 | Sponsor Protocol Number: IB3M.2019 | Start Date*: 2019-09-05 |
Sponsor Name:Universidad Complutense de Madrid | ||
Full Title: Efficacy of Non-Steroidal Anti-Inflammatory (Ibuprofen) Chronotherapy in Healing After Mandibular Third Molar Surgical Extraction – A Randomized Clinical Trial | ||
Medical condition: The clinical trial will try to understand if the elimination of the ibuprofen dosage in resting phase after surgical third molar extraction not jeopardize the postoperative period . | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006232-58 | Sponsor Protocol Number: UFC-08/01 | Start Date*: 2008-01-31 | ||||||||||||||||
Sponsor Name:Hospital general Universitario de Alicante | ||||||||||||||||||
Full Title: Ensayo clínico aleatorizado y controlado con paracetamol de la seguridad renal de metamizol en el tratamiento de pacientes cirróticos con y sin ascitis (Randomized Controlled Clinical Trial to stu... | ||||||||||||||||||
Medical condition: Dolor y/o fiebre en pacientes cirróticos con o sin descompensación ascítica | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002449-36 | Sponsor Protocol Number: ALGINF-2006/01 | Start Date*: 2006-10-23 | |||||||||||
Sponsor Name:Laboratorio de Aplicaciones Farmacodinámicas S.A. | |||||||||||||
Full Title: Ensayo clínico, multicéntrico, aleatorizado, simple ciego, paralelo, para evaluar la eficacia antipirética de lisinato de ibuprofeno versus ibuprofeno base en niños con procesos febriles. Multicent... | |||||||||||||
Medical condition: Procesos febriles en población infantil. Febrile processes in child population. | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005001-20 | Sponsor Protocol Number: HIVECR | Start Date*: 2015-05-21 |
Sponsor Name:DR. ALEJANDRO SOUSA ESCANDÓN | ||
Full Title: CHEMO-RESECTION WITH HYPERTHERMIC INTRAVESICAL INSTILLATION (HIVEC-R) VS STANDARD TREATMENT IN PATIENTS WITH NMIBT: COMPARATIVE, PROSPECTIVE AND RANDOMIZED STUDY OF EFFICACY AND TOLERABILITY | ||
Medical condition: NMIBT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004384-29 | Sponsor Protocol Number: Levosepsis1 | Start Date*: 2005-05-23 |
Sponsor Name:Dr GED DEMPSEY, University Hospital Aintree | ||
Full Title: Double blind randomised controlled trial of Levosimendan versus Dopexamine in septic shock | ||
Medical condition: Septic Shock | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003843-12 | Sponsor Protocol Number: PP-CT01 | Start Date*: 2017-01-16 |
Sponsor Name:PILA PHARMA | ||
Full Title: A Single-dose dose escalation trial in a randomised, single-blind, placebo-controlled group-comparison design to investigate the safety and tolerability of XEN-D0501 in 24 patients with diabetes me... | ||
Medical condition: Type 2 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010093-38 | Sponsor Protocol Number: HyRec | Start Date*: 2012-08-15 | ||||||||||||||||||||||||||
Sponsor Name:Dekan of the Medical Faculty of the University Erlangen-Nuremberg; Prof. Dr. Dr. h. c. Jürgen Schüttler | ||||||||||||||||||||||||||||
Full Title: Multi-institutional Phase I/II Study: Neoadjuvant chemoradiation with 5-FU (or capecitabine) and oxaliplatin combined with deep regional hyperthermia in locally advanced or recurrent rectal cancer | ||||||||||||||||||||||||||||
Medical condition: Locally advanced primary or locally recurrent rectal cancer | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003855-11 | Sponsor Protocol Number: 025/05 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Klinikum Großhadern, University of Munich / Medical Director: Prof. Dr. med. Burkhard Götze | |||||||||||||
Full Title: Gemcitabine and cisplatin in combination with hyperthermia in patients with locally advanced or metastatic pancreatic cancer as second-line therapy after adjuvant or first-line chemotherapy with Ge... | |||||||||||||
Medical condition: Combination of standard chemotherapy with Gemcitabine and Cisplatin and regional hyperthermia in patients with locally advanced or metastatic pancreatic cancer. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Restarted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000522-58 | Sponsor Protocol Number: NPM001 | Start Date*: 2014-10-02 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: A randomized, double blind, phase II trial of pazopanib versus placebo as maintenance therapy in patients with retroperitoneal and visceral high-risk soft tissue sarcomas following prior- and/or ad... | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000701-77 | Sponsor Protocol Number: AGO/2012/002 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Cytoreduction followed by Normothermic versus Hyperthermic Intraperitoneal Intraoperative Chemoperfusion: a Phase II Study in Peritoneal Carcinomatosis | |||||||||||||
Medical condition: Patients with peritoneal carcinomatosis from colorectal origin (including appendiceal mucinous neoplasms and the pseudomyxoma syndromes) amenable for cytoreduction and Hyperthermic Intraperitoneal ... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002628-18 | Sponsor Protocol Number: HIVECI | Start Date*: 2013-12-16 |
Sponsor Name:COMBAT MEDICAL LTD | ||
Full Title: HIVEC (Hyperthermic IntraVEsical Chemotherapy) FOR PATIENTS WITH INTERMEDIATE RISK NMIBC COMPARED WITH STANDARD INTRAVESICAL INSTILLATION OF CHEMOTHERAPY AS ADYUVANT TREATMENT. A COMPARATIVE, PROS... | ||
Medical condition: NON MUSCULAR INVASIVE BLADDER CANCER WITH INTERMEDIATE RISK OF RECURRENCE | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005428-99 | Sponsor Protocol Number: 08/0365 | Start Date*: 2009-10-19 | ||||||||||||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||||||||||||
Full Title: A randomised controlled phase III trial comparing hyperthermia plus mitomycin to a second course of bacillus Calmette-Guerin or standard therapy in patients with recurrence of non-muscle invasive b... | ||||||||||||||||||||||||||||
Medical condition: Non muscle invasive bladder cancer | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003830-34 | Sponsor Protocol Number: 415-13 | Start Date*: 2014-05-15 | |||||||||||
Sponsor Name:Asklepios Fachkliniken München Gauting | |||||||||||||
Full Title: Pleurectomy/decortication and hypterthermic intrathoracic chemotherapy compared to pleurectomy/decortication in patients with malignant pleural mesothelioma | |||||||||||||
Medical condition: malignant pleuramesothelioma | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
