- Trials with a EudraCT protocol (383)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (32)
383 result(s) found for: Effusion.
Displaying page 1 of 20.
EudraCT Number: 2007-006051-39 | Sponsor Protocol Number: KKS-110 | Start Date*: 2008-03-12 | |||||||||||
Sponsor Name:Philipps Universität Marburg | |||||||||||||
Full Title: Pharmakokinetic investigation on the tissue penetration of moxifloxacin within the pericardial space | |||||||||||||
Medical condition: Patients with chronic pericardial effusion , 5 of them with pericardial effusion indiced by malignancies, 10 of them with chronic inflammatory pericardial effusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 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: 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: 2012-005123-32 | Sponsor Protocol Number: SPON1030-11 | Start Date*: 2013-04-17 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: Oral steroids for the resolution of otitis media with effusion in children study (OSTRICH) | |||||||||||||
Medical condition: Otitis media with effusion. | |||||||||||||
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Population Age: Children, Under 18 | 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: 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: 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: 2006-003230-15 | Sponsor Protocol Number: BEV-EFF | Start Date*: 2006-10-17 |
Sponsor Name:University Clinic Internal Medicine I | ||
Full Title: Phase I/II study investigating increasing doses of bevacizumab in patients with malignant effusion | ||
Medical condition: Malignant effusion in cancer patients requiring frequent centesis, at least two within six weeks | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (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: 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: 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: 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: 2013-001849-13 | Sponsor Protocol Number: 2013/cardio3 | Start Date*: 2013-07-09 |
Sponsor Name:ASLTO2-Maria Vittoria Hospital Cardiology | ||
Full Title: AnakInRa Treatment of Recurrent Idiopathic Pericarditis | ||
Medical condition: idiopathic recurrent pericarditis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
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: 2009-011324-60 | Sponsor Protocol Number: DE-09-RG-53 | Start Date*: 2009-07-07 |
Sponsor Name:Hannover Medical School | ||
Full Title: Prospective randomized trial to compare a twice daily to a once daily administration of the Tacrolimus in lung transplanted patients | ||
Medical condition: Patients ( ≥18 and ≤ 70 years) ≥ 1 year after single, double or heart/lung transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
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: 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: 2006-002688-26 | Sponsor Protocol Number: BAY 43-9006 / 12006 | Start Date*: 2007-02-12 | |||||||||||
Sponsor Name:Bayer Healthcare AG, D-51368 Leverkusen, Germany | |||||||||||||
Full Title: A Phase III Randomized, Double-blind, Placebo Controlled Trial Comparing the Efficacy of Gemcitabine, Cisplatin and Sorafenib to Gemcitabine, Cisplatin and Placebo in First-Line Treatment of Patien... | |||||||||||||
Medical condition: The patient population includes patients with Stage IIIB (with effusion) or Stage IV NSCLC of non-squamos cell carcinoma subtype, with ECOG performance status 0 or 1, for whom treatment with gemci... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) BE (Completed) FI (Completed) GR (Completed) AT (Completed) GB (Completed) IT (Completed) NL (Completed) HU (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004051-19 | Sponsor Protocol Number: IM101-042 | Start Date*: 2005-05-13 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: A Phase IIB, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Abatacept in Combination Therapy with Glucocorticosteroids vs. Placebo plus Gluc... | ||
Medical condition: SYSTEMIC LUPUS ERYTHEMATOSUS, NOS | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) BE (Completed) AT (Completed) IT (Prematurely Ended) | ||
Trial results: Removed from public view |
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