- Trials with a EudraCT protocol (280)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
280 result(s) found for: Pleural effusion.
Displaying page 1 of 14.
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: 2019-003542-32 | Sponsor Protocol Number: SCOPE | Start Date*: 2020-02-28 |
Sponsor Name:Dr. José Manuel Porcel Pérez | ||
Full Title: Randomised clinical trial: saline washouts versus standard treatment in complicated parapneumonic pleural effusion or empyema. SCOPE study. | ||
Medical condition: Treatment of complicated parapneumatic pleural effusion or empyema | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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: 2014-003137-25 | Sponsor Protocol Number: ODAPE | Start Date*: 2014-12-26 |
Sponsor Name:José Manuel Porcel Pérez Hospital Arnau de Vilanova de Lleida Servicio Medicina Interna | ||
Full Title: Optimal duration of antibiotic treatment in patients with complicated parapneumonic pleural effusions or empyema: a randomized clinical trial | ||
Medical condition: Duration of antibiotic treatment in complicated parapneumonic pleural effusion and empyema. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000658-22 | Sponsor Protocol Number: PROT 1203 | Start Date*: 2005-06-16 |
Sponsor Name:University of Oxford, NDM | ||
Full Title: The Second Multi-Centre Intra-Pleural Sepsis Trial (MIST2), to assess whether DNase or Alteplase improves pleural fluid drainage in pleural infection. | ||
Medical condition: Empyema and complicated parapneumonic pleural effusion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002221-35 | Sponsor Protocol Number: P2013/PE1 | Start Date*: 2014-12-18 | ||||||||||||||||
Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola | ||||||||||||||||||
Full Title: Prospective Randomized Study Comparing the Efficacy and Safety of Pleural Drainage by Video-Assisted Thoracoscopic With Pleural Drain Associated With Urokinase in the Treatment of Parapneumonic Ple... | ||||||||||||||||||
Medical condition: Parapneumonic pleural effusion | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000559-35 | Sponsor Protocol Number: 0 | Start Date*: 2022-07-14 |
Sponsor Name:None | ||
Full Title: COMPLICATIONS AND DEGREE OF TOLERANCE OF THE ADMINISTRATION OF LOCAL ANESTHESIA IN DIAGNOSTIC / THERAPEUTIC THORACOCENTESIS PROCEDURES | ||
Medical condition: There is no consensus about the most appropriate local anesthetic, and 1% mepicavain and 2% lidocaine uses can be postulated indistinctly. This project was born with the intention of highlighting t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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: 2006-005122-23 | Sponsor Protocol Number: 0683-056 | Start Date*: 2008-08-06 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase II/III Randomized, Double-Blind Study of Paclitaxel plus Carboplatin in Combination with Vorinostat (MK-0683) or Placebo in Patients with Stage IIIB (with pleural effusion) or Stage IV Non-... | |||||||||||||
Medical condition: Stage IIIB (with pleural effusion) or Stage IV Non-Small-Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Prematurely Ended) FI (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) IT (Prematurely Ended) LV (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2007-001795-37 | Sponsor Protocol Number: AMB TS | Start Date*: 2007-07-19 |
Sponsor Name:Medical University Innsbruck, Dpt. Internal Medicine, Div. Internal Medicine | ||
Full Title: WIRKORTKONZENTRATIONEN VON AMPHOTERICIN B FORMULIERUNGEN IN ASZITES, LIQUOR, PLEURAERGUSS, GALLE UND LIQUOR BEI KRITISCH KRANKEN (Target-site concentrations of Amphotericin B preparations in ascit... | ||
Medical condition: Plasma and target-site (ascites, pleural effusion, bile and cerebrospinal fluid) concentrations of amphotericin B preparations will be measured in critically ill patients, requiring treatment with ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
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: 2013-005065-38 | Sponsor Protocol Number: ECHI-TS-2 | Start Date*: 2014-02-17 |
Sponsor Name:Medizinische Universität Innsbruck, Universitätsklinik für Innere Medizin I | ||
Full Title: Concentrations of echinocandins in ascites, pleural effusion, bile, wound secretion and cerebrospinal fluid – a pilot study | ||
Medical condition: Invasive fungal infection treated with an echinocandin and indication for paracentesis, thoracentesis, bile deviation or sampling, lumbar puncture or VAC therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
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: 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: 2009-012963-33 | Sponsor Protocol Number: CORTEEC | Start Date*: 2010-10-04 | |||||||||||
Sponsor Name:ALFREDO TAGARRO GARCIA | |||||||||||||
Full Title: ENSAYO CLINICO FASE II CORTICOIDES PARA EL EMPIEMA Y EL DERRAME PLEURAL PARANEUMÓNICO EN NIÑOS MULTICENTRIC, PHASE II, CLINICAL TRIAL CORTICOIDS FOR EMPYEMA AND PLEURAL EFFUSION IN CHILDREN | |||||||||||||
Medical condition: DERRAME PLEURAL PARANEUMONICO (PARAPNEUMONIC PLEURAL EFFUSSION) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Restarted) | |||||||||||||
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 |
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