- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
67 result(s) found for: Effervescent Tablet.
Displaying page 1 of 4.
EudraCT Number: 2010-023485-53 | Sponsor Protocol Number: IJG-PAR-2010 | Start Date*: 2011-04-20 |
Sponsor Name:IDIAP JORDI GOL I GURINA | ||
Full Title: Evaluation of the relationship between effervescent acetaminophen and blood pressure. A clinical trial. | ||
Medical condition: Evaluation of whether paracetamol effervescent formulation increases blood pressure compared with effervescent paracetamol formulation does not | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002754-22 | Sponsor Protocol Number: BUM-4/GVH | Start Date*: 2006-03-14 |
Sponsor Name:Dr. Falk Pharma GmbH | ||
Full Title: An open, randomized, multicentre phase II pilot study to evaluate the efficacy of budesonide 3 mg effervescent tablet in patients with resistant oral chronic GvHD using different application durati... | ||
Medical condition: oral chronic graft versus host disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-006117-16 | Sponsor Protocol Number: Puranik 07-03/23 | Start Date*: 2008-07-31 |
Sponsor Name:Betsi Cadwaladr University Health Board | ||
Full Title: A prospective, randomised, phase IV, open label clinical trial to study the therapeutic use of buprenorphine 20 mg (BuTrans 20µg/h) matrix transdermal patch in the management of post tonsillectomy ... | ||
Medical condition: post-tonsillectomy pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001484-12 | Sponsor Protocol Number: BUL-1/EEA | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase III trial on the efficacy and tolerability of a 6-week treatment with budesonide effervescent tablets vs. placebo for induction of clinico-pathol... | |||||||||||||
Medical condition: Active eosinophilic esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016692-29 | Sponsor Protocol Number: BUU-2/EEA | Start Date*: 2012-02-20 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, double-dummy, randomized, placebo-controlled, phase IIa study on the efficacy and tolerability of a 14-day treatment with budesonide effervescent tablets vs. viscous budesonide suspen... | |||||||||||||
Medical condition: Active eosinophilic esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001485-99 | Sponsor Protocol Number: BUL-2/EER | Start Date*: 2015-12-08 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled, phase III study on the efficacy and tolerability of a 48-week treatment with two different doses of budesonide effervescent tablets vs. placebo for mai... | |||||||||||||
Medical condition: Maintenance of remission in eosinophilic esophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) NL (Completed) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005040-35 | Sponsor Protocol Number: 0120 | Start Date*: 2021-01-28 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The effect of effervescent and buffered alendronate on bone turnover compared to conventional alendronate: A randomized non-inferiority trial | |||||||||||||
Medical condition: Osteopenia, i.e. bone mineral density T-score < -1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003570-11 | Sponsor Protocol Number: BC-6072 | Start Date*: 2019-10-21 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: The use of buffered soluble alendronate 70 mg (Steovess/Binosto) after denosumab discontinuation to prevent increase in bone turnover. | |||||||||||||
Medical condition: erosive osteoarthritis of the interphalangeal finger joints | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006837-28 | Sponsor Protocol Number: PML_DOC_0804 | Start Date*: 2008-12-08 |
Sponsor Name:University Hospital Antwerp; Department Respiratory Medicine | ||
Full Title: Double blind, randomized, placebo-controlled, two-way crossover, pilot study to assess the effect of high dose N-acetylcysteine on small airways and on inflammation and oxidative stress in COPD pat... | ||
Medical condition: Chronic Obstructive Pulmonary Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003946-13 | Sponsor Protocol Number: PML_NAC_01 | Start Date*: 2007-09-05 |
Sponsor Name:University Hospital Antwerp; Department Respiratory Medicine | ||
Full Title: Double blind, randomized, placebo-controlled, two-way crossover, pilot study to assess the effect of high dose N acetylcysteine on small airways and on inflammation and oxidative stress in COPD pat... | ||
Medical condition: Chronic Obstructive Pulmonary Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000060-20 | Sponsor Protocol Number: 2018-08-EFT-1 | Start Date*: 2019-12-20 | |||||||||||
Sponsor Name:HEXAL AG | |||||||||||||
Full Title: Efficacy and safety of acetylcysteine for the treatment of acute uncomplicated rhinosinusitis: a prospective, randomized, double-blind, placebo-controlled trial | |||||||||||||
Medical condition: Acute rhinosinusitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004562-10 | Sponsor Protocol Number: BUM-5/GVH | Start Date*: 2009-07-29 | |||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomised, placebo-controlled multicentre phase III clinical study followed by open-label phase on the efficacy and tolerability of budesonide 3 mg effervescent tablet in patients wi... | |||||||||||||
Medical condition: Oral chronic graft versus host disease as a complication of haematopoietic stem cell transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Completed) FR (Completed) SE (Completed) IT (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004466-14 | Sponsor Protocol Number: RH01361 | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: Effects of two doses of a common cold treatment on cognitive function | |||||||||||||
Medical condition: Common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002322-12 | Sponsor Protocol Number: Ironsuppletiontrial | Start Date*: 2014-07-24 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Optimizing Iron suppletion trial after Roux- en -Y Gastric Bypass | ||
Medical condition: Patients who underwent a gastric bypass and develop an irondeficiency postoperatively. The medical condition which is investigated is irondeficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002323-10 | Sponsor Protocol Number: absorptiontrial | Start Date*: 2014-07-21 |
Sponsor Name:Rijnstate | ||
Full Title: Iron absorptiontrail after Roux- en -Y Gastric Bypass | ||
Medical condition: Patients who are eligible for a primary Roux- en -Y gastric bypass and who have no irondificiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012707-26 | Sponsor Protocol Number: Acetilcisteina-Ocronosi-SI/2009 | Start Date*: 2010-05-27 |
Sponsor Name:AZIENDA OSPEDALIERA SENESE | ||
Full Title: THERAPEUTIC EFFECTIIVENESS OF N-ACETYL-CYSTEINE AND ASCORBIC ACID IN PATIENTS WITH ALKAPTONURIA-OCHRONOSIS | ||
Medical condition: patient affected by alkaptonuria-ocronosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005015-17 | Sponsor Protocol Number: GE09-01 | Start Date*: 2009-05-13 |
Sponsor Name:VU university medical centre | ||
Full Title: Effect of N-acetylcysteine on thiopurine related hepatotoxicity in IBD patients | ||
Medical condition: adult patients (18-70 years old) who have been treated with azathioprine, 6-mercaptopure or 6-thioguanine for inflammatory bowel disease, in whom hepatotoxicity occured as an adverse event, are eli... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005809-38 | Sponsor Protocol Number: NACP1 | Start Date*: 2006-12-08 |
Sponsor Name:Research & Development Department, Addenbrookes Hospital | ||
Full Title: Does prophylactic N acetylcysteine reduce the incidence of contrast nephropathy in patients undergoing peripheral angiography | ||
Medical condition: We will use N acetylcystiene prophylactically in patient undergoing peripheral angiography at the Cambridge Vascular Unit at Addenbrooke's Hospital in order to prevent renal injury. Patients underg... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003651-12 | Sponsor Protocol Number: NAC-E-23 | Start Date*: 2005-11-11 |
Sponsor Name:ZAMBON, S.A. | ||
Full Title: NAC EFFECT ON OXIDATIVE STRESS AND MUSCLE FUNCTION IN COPD PATIENTS. Efecto de NAC en estrés oxidativo y función muscular en pacientes con EPOC | ||
Medical condition: CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD). | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001098-25 | Sponsor Protocol Number: NAC-E-21 | Start Date*: 2004-08-23 |
Sponsor Name:Zambon SA | ||
Full Title: N-Acetylcisteine (NAC) effect on the inmunologycal system | ||
Medical condition: Postmenopausal health woman aged more than 50 years | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
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