- Trials with a EudraCT protocol (261)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (47)
261 result(s) found for: Diarrhoea.
Displaying page 1 of 14.
EudraCT Number: 2012-002291-13 | Sponsor Protocol Number: DIALAGG | Start Date*: 2012-10-19 | |||||||||||
Sponsor Name:InfectoPharm - Arzneimittel und Consilium GmbH | |||||||||||||
Full Title: Multicentre, prospective, double-blind, two-armed, placebo-controlled phase III study to evaluate the efficacy and safety of the treatment of diarrhoea with Lactobacillus rhamnosus GG (InfectoDiarr... | |||||||||||||
Medical condition: Acute diarrhoea in infants and toddlers | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002217-22 | Sponsor Protocol Number: SJ-546 | Start Date*: 2016-09-02 | ||||||||||||||||
Sponsor Name:Sjællands University Hospital, Køge | ||||||||||||||||||
Full Title: Validation of stimulated ∆FGF19 for diagnosing bile acid diarrhoea | ||||||||||||||||||
Medical condition: Bile acid malabsorption / bile acid diarrhoea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001452-22 | Sponsor Protocol Number: SJ-641 | Start Date*: 2018-08-29 | ||||||||||||||||
Sponsor Name:Zealand University Hospital | ||||||||||||||||||
Full Title: Treatment effect of colesevelam for bile acid diarrhoea | ||||||||||||||||||
Medical condition: Bile acid diarrhoea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004291-39 | Sponsor Protocol Number: Clin-AGI004-002 | Start Date*: 2008-09-09 | |||||||||||
Sponsor Name:AGI Therapeutics Research Ltd | |||||||||||||
Full Title: A randomised, multi-centre, double-blind, balanced, parallel group placebo-controlled study of AGI004 for the control of chemotherapy-induced diarrhoea. | |||||||||||||
Medical condition: Chemotherapy-induced diarrhoea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003777-28 | Sponsor Protocol Number: OBADIAH1 | Start Date*: 2012-04-26 |
Sponsor Name:Imperial College London and Imperial College Healthcare NHS Trust | ||
Full Title: Obeticholic acid treatment in patients with bile acid diarrhoea: an open-label, pilot study of mechanisms, safety and symptom response. | ||
Medical condition: Bile acid diarrhoea (also known as bile acid malabsorption) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017374-20 | Sponsor Protocol Number: BNI-2009-01 | Start Date*: 2010-04-19 | |||||||||||||||||||||
Sponsor Name:Bernhard-Nocht-Institute for Tropical Medicine | |||||||||||||||||||||||
Full Title: Probiotic Saccharomyces boulardii for the prevention of antibiotic-associated diarrhoea – randomised, double-blind, placebo-controlled trial | |||||||||||||||||||||||
Medical condition: Antibiotic - associated - Diarrhoea (AAD) Clostridium difficile - associated - Diarrhoea (CDAD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000256-28 | Sponsor Protocol Number: LAP117314 | Start Date*: 2014-08-21 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Randomised, Multicentre, Open Label, Phase II study of Prophylactic Octreotide to Prevent or Reduce the Frequency and Severity of Diarrhoea in Subjects Receiving Lapatinib with Capecitabine for t... | |||||||||||||
Medical condition: Diarrhoea associated with treatment with lapatinib and capecitabine for metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) IT (Completed) GR (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003986-42 | Sponsor Protocol Number: Rifa1 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:University Hospital of Tübingen | |||||||||||||
Full Title: Prospective, randomised, placebo controlled, double blind monocenter trial for the prophylactic treatment of diarrhoea with rifaximin for travellers to South- and Southeast-Asia | |||||||||||||
Medical condition: diarrhoea of travellers to South- and Southeast-Asia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023347-14 | Sponsor Protocol Number: 2010-10 | Start Date*: 2011-03-02 | |||||||||||
Sponsor Name:Gastroenterology CHC Liege | |||||||||||||
Full Title: Treatment of Crohn’s disease-associated refractory diarrhoea with octreotide LAR An open pilot study | |||||||||||||
Medical condition: Crohn Disease refractory diarrhoea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004740-35 | Sponsor Protocol Number: s-20140081 | Start Date*: 2014-12-19 | |||||||||||
Sponsor Name:Department of surgery, Odense University Hospital | |||||||||||||
Full Title: Loperamide vs. Placebo's effect on ileostomy output: A clincal randomized patientblinded crossover study | |||||||||||||
Medical condition: Patients with ileostomy because of ulcerative colitis, rectal cancer or short bowel syndrom | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002948-28 | Sponsor Protocol Number: Loop | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:MAROS Arzneimittel GmbH | |||||||||||||
Full Title: Prospective randomized monoinstitutional study of the treatment of therapy-associated diarrhea during percutaneous radiation therapy of the small pelvis. – Comparison of loperamide and tincture of ... | |||||||||||||
Medical condition: Therapy-associated diarrhea during radiaton therapy of small pelvis (including enteritis as a result of radiation therapy and enteritis as a result of radiation- and chemotherapy). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002876-32 | Sponsor Protocol Number: AAD-CDD-001 | Start Date*: 2008-10-06 | |||||||||||
Sponsor Name:University of Wales Swansea | |||||||||||||
Full Title: A multicentre, randomised, placebo controlled trial of lactic acid bacteria in the prevention of antibiotic-associated diarrhoea (AAD) and Clostridium difficile diarrhoea (CDD) in patients aged 65 ... | |||||||||||||
Medical condition: AAD is diarrhoea occurring in association with antibiotic treatment without an alternative cause. It occurs typically 2-8 weeks after exposure to antibiotics. The frequency of AAD varies markedly b... | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005244-16 | Sponsor Protocol Number: CDiffPrevTrial1 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:Wrightington, Wigan and Leigh NHS Trust | |||||||||||||
Full Title: Probiotics for the prevention of Antibiotics associated diarrhoea and Clostridium difficile associated diarrhoea A multi-centre, double-blind, randomized placebo controlled trial | |||||||||||||
Medical condition: Prevention of Clostridium Difficile associated diarrhoea. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002290-25 | Sponsor Protocol Number: FEBATRIC | Start Date*: 2022-02-10 |
Sponsor Name:Nadační fond Donatio intensivistam | ||
Full Title: Faecal bacteriotherapy for postantibiotic diarrhoea in critically ill patients | ||
Medical condition: Postantibiotic diarrhoea | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001054-84 | Sponsor Protocol Number: 2004/W/GI/02 | Start Date*: 2005-02-16 |
Sponsor Name:NHS Lothian- University Hospitals Division | ||
Full Title: A comparison of the efficacy of dietary hydroxypropylcellulose and questran as therapeutic agents in bile acid induced diarrhoea | ||
Medical condition: these patients will have bile acid induced diarrhoea identified by an increased serum 7a-OH-cholestenone. and will have a history of one of 1. ileal resection 2. idiopathic bile acid diarrhoea.3. ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-006269-17 | Sponsor Protocol Number: SPON1069-11 | Start Date*: 2012-11-16 | |||||||||||
Sponsor Name:Cardiff University, Research & Development Commercial Department | |||||||||||||
Full Title: A double blind placebo controlled randomised clinical trial to study the effect of Probiotics for the prevetion or amelioration of Antibiotic Associated Diarrhoea in residents of care homes in Sout... | |||||||||||||
Medical condition: Antibiotic Associated Diarrhoea | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004473-16 | Sponsor Protocol Number: SL001-2.0 | Start Date*: 2016-07-19 |
Sponsor Name:Masarykův onkologický ústav | ||
Full Title: Prospective study investigating efficacy of lanreotide on decrease of chemotherapy induced diarrhoea (CID) in patiens with colorectal carcinoma. | ||
Medical condition: Chemotherapy induced diarrhoea that is resistant to common treatment including loperamide in patients with colorectal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003220-21 | Sponsor Protocol Number: GA19/105668 | Start Date*: 2020-02-26 | |||||||||||||||||||||
Sponsor Name:University of Leeds | |||||||||||||||||||||||
Full Title: Management of diarrhoea in ulcerative colitis: multi-arm multi-stage trial of low FODMAP diet, amitriptyline, ondansetron, or loperamide: MODULATE. | |||||||||||||||||||||||
Medical condition: Diarrhoea in patients with stable ulcerative colitis. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001559-38 | Sponsor Protocol Number: GEICAM/2018-06 | Start Date*: 2022-01-20 | ||||||||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | ||||||||||||||||||
Full Title: A Randomized Phase II Study to Evaluate the Incidence of Discontinuations due to Diarrhoea at 3 Cycles in patients with Early-stage HER2-positive (HER2+), Hormone Receptor-positive (HR+) Breast Can... | ||||||||||||||||||
Medical condition: HER2+, HR+ Early stage Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004291-12 | Sponsor Protocol Number: 101.1.C.004 | Start Date*: 2008-08-18 | |||||||||||
Sponsor Name:Optimer Pharmaceuticals, Inc. | |||||||||||||
Full Title: A multi-national, multi-centre, double-blind, randomised, parallel group study to compare the safety and efficacy of 200mg PAR-101 taken q12h with 125mg Vancomycin taken q6h for ten days in subject... | |||||||||||||
Medical condition: Clostridium difficile associated diarrhoea (CDAD) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) ES (Completed) FR (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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