- Trials with a EudraCT protocol (149)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
149 result(s) found for: Malignant pleural effusion.
Displaying page 1 of 8.
EudraCT Number: 2012-000599-40 | Sponsor Protocol Number: | Start Date*: 2012-06-13 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:North Bristol NHS Trust | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The efficacy of Indwelling Pleural Catheter placement versus IPC placement PLUS sclerosant (talc) in patients with malignant pleural effusions managed exclusively as out-patients | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Malignant pleural effusions | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018275-20 | Sponsor Protocol Number: UMCNONCO201001 | Start Date*: 2010-03-24 | ||||||||||||||||
Sponsor Name:University Medical Centre Nijmegen St Radboud | ||||||||||||||||||
Full Title: A phase II study of cediranib as palliative treatment in patients with symptomatic malignant ascites or pleural effusion | ||||||||||||||||||
Medical condition: symptomatic malignant ascites or pleural effusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000586-26 | Sponsor Protocol Number: TIME3UK | Start Date*: 2009-03-20 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Adjuvant Urokinase in the Treatment of Malignant Pleural Effusion: The Third Therapeutic Intervention in Maligant Effusion Trial (TIME3-UK). A Randomised Controlled Trial to evaluate whether use of... | |||||||||||||
Medical condition: Patients with malignant pleural effusions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005226-31 | Sponsor Protocol Number: 1.1 | Start Date*: 2006-04-24 |
Sponsor Name:University of Oxford, Nuffield Department of Medicine | ||
Full Title: TIME 1 The First Therapeutic Intervention in Malignant Pleural Effusion Trial (TIME1) A 2 x 2 randomised factorial trial to assess whether non-steroidal anti-inflammatory analgesics and small bore... | ||
Medical condition: Malignant pleural effusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009134-32 | Sponsor Protocol Number: 2137/09 | Start Date*: 2009-04-27 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: Bristol Randomised Controlled Trial of Zoledronic Acid in Malignant Pleural disease(Pilot Study). | ||
Medical condition: Malignant pleural disease of all histological cell types. 50% patients in trial will have indwelling pleural catheters for management of breathlessness. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001121-24 | Sponsor Protocol Number: P00804 | Start Date*: 2011-04-21 |
Sponsor Name:Papworth Hospital NHS Trust | ||
Full Title: Prospective randomised controlled trial of video assisted thorascopic (VATS) cytoreductive pleurectomy compared to talc pleurodesis in patients with suspected or proven malignant mesothelioma | ||
Medical condition: Mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004727-23 | Sponsor Protocol Number: 3850 | Start Date*: 2017-06-19 | |||||||||||
Sponsor Name:North Bristol NHS Trust Research & Innovation | |||||||||||||
Full Title: A Trial of Intra-pleuraL OK-432 Therapy in mesothelioma (TILT): A feasibility study using the ‘trial within a cohort’ methodology | |||||||||||||
Medical condition: Malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005831-13 | Sponsor Protocol Number: CDKO-125a-005 | Start Date*: 2009-02-17 | |||||||||||
Sponsor Name:NERVIANO MEDICAL SCIENCES | |||||||||||||
Full Title: Phase II study of PHA-848125AC as second line-treatment in pemetrexed pre-treated malignant pleural mesothelioma patients | |||||||||||||
Medical condition: Malignant Pleural Mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003664-22 | Sponsor Protocol Number: 2006/26 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO | |||||||||||||
Full Title: INTRAPLEURAL PACLITAXEL IN PATIENTS WITH MALIGNANT PLEURAL EFFUSIONS SECONDARY TO OVARIAN CANCER AND OTHER NEOPLASMS | |||||||||||||
Medical condition: MALIGNANT PLEURAL EFFUSION SECONDARY TO OVARIAN, BREAST OR LUNG CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005621-24 | Sponsor Protocol Number: N14PLU | Start Date*: 2014-07-17 | ||||||||||||||||
Sponsor Name:Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | ||||||||||||||||||
Full Title: PeRsOnalized treatment fOr patients with pleural eFfusions due to malignant pleural mesothelioma or lung cancer in second or third line. An open label phase II study (Acronym: the PROOF study) | ||||||||||||||||||
Medical condition: Proven pleural effusion of malignant pleural mesothelioma or non small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001731-30 | Sponsor Protocol Number: CDP791-002 | Start Date*: 2005-07-25 |
Sponsor Name:UCB Celltech | ||
Full Title: A Two-Part, Open Label Phase II Trial: Part One, Dose Escalation Safety; Part Two, Randomized/Comparing CDP791 (10 or 20 mg/kg) Plus Carboplatin/Paclitaxel With Carboplatin/Paclitaxel Alone in Sub... | ||
Medical condition: Non squamous non small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002625-77 | Sponsor Protocol Number: DCT1 | Start Date*: 2007-07-03 | |||||||||||
Sponsor Name:FONDAZIONE ISTITUTO SAN RAFFAELE-G.GIGLIO | |||||||||||||
Full Title: Randomized phase II trial of first line chemoterapy Docetaxel given in combination with Cisplatin for 6 cycles or Docetaxel given in combination with Cisplatin for 3 cycles followed by Docetaxel al... | |||||||||||||
Medical condition: Patients with advanced non-small-cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001494-15 | Sponsor Protocol Number: 311135 | Start Date*: 2008-07-08 |
Sponsor Name:Bayer Schering Pharma | ||
Full Title: Phase I/II Study of Sagopilone in combination with carboplatin and bevacizumab in the first-line treatment of patients with stage IIIB/IV, non-squamous NSCLC. | ||
Medical condition: Treatment of patients with non-squamous NSCLC, Stage IIIB (with malignant pleural effusion) or Stage IV disease with no prior systemic treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-004030-40 | Sponsor Protocol Number: TOGA 0502 | Start Date*: 2006-02-06 |
Sponsor Name:Thoracale Oncologie Groep Antwerpen | ||
Full Title: A RANDOMIZED MULTICENTER PHASE II STUY OF INDUCTION THERAPY WITH PEMETREXED AND CISPLATIN FOLLOWED BY CHEMORADIATION WITH PEMETREXED VERSUS CHEMORADIATION WITH PEMETREXED FOLLOWED BY CONSOLIDATION ... | ||
Medical condition: Non-Small Cell Lung Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002425-52 | Sponsor Protocol Number: H3E-MC-JMEN(a) | Start Date*: 2005-03-24 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: A Phase 3 Study of Pemetrexed Plus Best Supportive Care versus Best Supportive Care As Maintenance Therapy Immediately Following Induction Treatment For Advanced Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: Non Small Cell Lung Cancer Stage IIIB or Stage IV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) AT (Completed) HU (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000971-41 | Sponsor Protocol Number: GGCP032/07 | Start Date*: 2007-07-03 | ||||||||||||||||
Sponsor Name:Grupo Gallego de Cáncer de Pulmón | ||||||||||||||||||
Full Title: Estudio fase II de bevacizumab en combinación con vinorelbina y cisplatino, como tratamiento de primera línea de pacientes con cáncer de pulmón no microcítico,no epidermoide, estadio IIIB con derra... | ||||||||||||||||||
Medical condition: Cáncer de pulmón no microcítico(CPNM), no epidermoide, estadio IIIB con derrame pleural o IV / on-small cell, non-squamous lung cancer, stage IIIb with pleural effusion or stage IV. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001990-32 | Sponsor Protocol Number: NOV002-C301 | Start Date*: 2006-11-22 | |||||||||||
Sponsor Name:NOVELOS THERAPEUTICS INC. | |||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Trial of NOV-002 in Combination with Paclitaxel and Carboplatin vs. Paclitaxel and Carboplatin Alone for the Treatment of Advanced Non-Small-Cell Lung Cancer (NS... | |||||||||||||
Medical condition: Patients with advanced NSCLC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003894-18 | Sponsor Protocol Number: M07CCL | Start Date*: 2008-01-30 |
Sponsor Name:NKI-AVL | ||
Full Title: Open-label, randomised, multi-center study investigating Cetuximab, in combination with concurrent chemo- / radiotherapy in locally advanced non-small cell lung carcinoma | ||
Medical condition: Non-small cell lung cancer locally advanced | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010571-24 | Sponsor Protocol Number: VEG111109 | Start Date*: 2009-08-03 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||||||||||||||||||
Full Title: An open label, multicenter, Phase I/II study of pazopanib in combination with paclitaxel in first line treatment of subjects with stage IIIBwet/IV non-small cell lung cancer | ||||||||||||||||||
Medical condition: Part I: Subjects with histologically or cytologically confirmed diagnosis of advanced solid tumours for which there is no standard therapy or for whom paclitaxel is standard therapy. Part II: Sta... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002035-33 | Sponsor Protocol Number: 65 plus | Start Date*: 2009-04-20 |
Sponsor Name:Martha-Maria Krankenhaus Halle-Dölau gGmbH | ||
Full Title: Open-label study of Bevacizumab (AVASTIN®) in combination with Pemetrexed or Pemetrexed and Carboplatin as first-line treatment of patients with advanced or recurrent non-squamous non-small cell lu... | ||
Medical condition: Patients with advanced metastatic or recurrent non- small cell lung cancer (NSCLC). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
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