- Trials with a EudraCT protocol (65)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
65 result(s) found for: Feces.
Displaying page 1 of 4.
EudraCT Number: 2006-002739-25 | Sponsor Protocol Number: P/PFI/01 | Start Date*: 2006-09-15 | |||||||||||
Sponsor Name:S.L.A. Pharma (UK) Ltd | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled study to evaluate topical 10%phenylephrine gel applied peri-anally in the management of ileal pouch anal anastomosis (IPAA)-related faecal incontinence | |||||||||||||
Medical condition: Ileal pouch anal anastomosis (IPAA)-related faecal incontinence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021659-17 | Sponsor Protocol Number: CMMAd/InFe/2011 | Start Date*: 2013-08-14 | |||||||||||
Sponsor Name:Fundación Pública Andaluza Progreso y Salud | |||||||||||||
Full Title: Phase I / II, multicenter, double blind, randomized, comparison of two groups and two doses, to evaluate the safety and efficacy of autologous ASCs in the treatment of fecal incontinence. | |||||||||||||
Medical condition: Patients with incontinence faecal | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003817-12 | Sponsor Protocol Number: 2021/0384/HP | Start Date*: 2023-05-15 | |||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||
Full Title: Mechanisms of action on rectal motility of intrarectal botulinum toxin injections in patients with fecal incontinence | |||||||||||||
Medical condition: Patients with fecal incontinence who have failed conservative treatments and are candidates for intrarectal botulinum toxin injections. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005399-21 | Sponsor Protocol Number: IC-01-02-2-010 | Start Date*: 2022-02-14 | |||||||||||
Sponsor Name:Innovacell AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation for the treatment of fecal incontinence: a single arm, open label, interventional, follow-up study | |||||||||||||
Medical condition: Fecal incontinence (FI) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021463-32 | Sponsor Protocol Number: IC-01-02-02-007 | Start Date*: 2011-02-24 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation for the treatment of fecal incontinence: a multicenter, randomized, double-blind, placebocontrolled, parallel-group, dose-finding clinical study | |||||||||||||
Medical condition: Fecal incontinence in female and male patients with external anal sphincter weakness or sphincter damage. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) SI (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002331-34 | Sponsor Protocol Number: ALOFEC-2019 | Start Date*: 2022-11-08 | |||||||||||
Sponsor Name:FIMABIS | |||||||||||||
Full Title: A multicenter, randomized, double-blind Phase IIb study to evaluate the safety and efficacy of the intralesional administration of two doses of expanded allogeneic adipose tissue adult stem mesench... | |||||||||||||
Medical condition: Fecal incontinence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003206-25 | Sponsor Protocol Number: NRL001-01/2011(SEFI) | Start Date*: 2012-01-25 | |||||||||||
Sponsor Name:Norgine Ltd | |||||||||||||
Full Title: A multi-centre, phase II, double-blind, randomised, placebo-controlled, parallel group, dose-ranging study in patients with faecal incontinence; to evaluate the efficacy, safety and tolerability of... | |||||||||||||
Medical condition: Faecal incontinence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) DE (Completed) ES (Completed) GB (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2021-001376-42 | Sponsor Protocol Number: IC-01-02-5-009 | Start Date*: 2021-10-27 | ||||||||||||||||
Sponsor Name:Innovacell AG | ||||||||||||||||||
Full Title: Skeletal muscle-derived cell implantation for the treatment of fecal incontinence: a phase III, randomized, controlled, double blind, two armed clinical study. | ||||||||||||||||||
Medical condition: Fecal incontinence | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) BG (Trial now transitioned) AT (Ongoing) PL (Trial now transitioned) CZ (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003048-11 | Sponsor Protocol Number: GIPIT002 | Start Date*: 2014-10-24 |
Sponsor Name:GIPIT | ||
Full Title: FEcal transplant, a Dazzling debut to Eradicate colonization with eXtreme drug resistant bacteria? | ||
Medical condition: Patient harboring Extreme Drug Resistant (XDR) bacteria. Our trial try to eradicate this digestive tract colonization by performing a fecal transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004940-31 | Sponsor Protocol Number: 18122019 | Start Date*: 2020-03-24 | |||||||||||
Sponsor Name:Terese Katzenstein | |||||||||||||
Full Title: Effect of timing of enzyme replacement therapy (Creon®) at meals on fat malabsorption in adult patients with cystic fibrosis - a cross-over trial | |||||||||||||
Medical condition: GI pains and fat malabsorption in cystic fibrosis patients with pancreas insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004979-39 | Sponsor Protocol Number: MSP-2017-1220 | Start Date*: 2020-08-06 |
Sponsor Name:Milestone Pharmaceuticals Inc. | ||
Full Title: An open-label, mass balance study to investigate the absorption, distribution, metabolism and excretion of [14C]-etripamil nasal spray after a single dose to healthy male subjects | ||
Medical condition: Paroxysmal supraventricular tachycardia (PSVT) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001317-28 | Sponsor Protocol Number: ABBA-2 | Start Date*: 2015-07-30 |
Sponsor Name:UMC Utrecht | ||
Full Title: A B2-agonist as a CFTR activator in CF - Part 2 | ||
Medical condition: Cystic fibrosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004248-39 | Sponsor Protocol Number: PPI-microbiome | Start Date*: 2018-01-04 |
Sponsor Name:TARGID, KU Leuven | ||
Full Title: Effect of Proton Pump Inhibitors on the duodenal microbiome in healthy volunteers | ||
Medical condition: We will assess the effect of Proton Pump Inhibitors (PPI) on the duodenal, oral and fecal microbiota composition in healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002707-32 | Sponsor Protocol Number: IC4-05682-031-CZE | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:SERVIER s.r.o. | |||||||||||||
Full Title: HEMODEX study- Detralex* versus placebo in the treatment of acute hemorrhoids in patients with acute hemorrhoidal attack. One week, double-blind, randomized, placebo controlled, multicentre study. | |||||||||||||
Medical condition: Acute hemorrhoidal attack (stage I, II, III) taking no longer than 48 hours | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002963-23 | Sponsor Protocol Number: Not available | Start Date*: 2006-08-03 |
Sponsor Name:Chr. Hansen A/S | ||
Full Title: The effect of probiotics on bloating in IBS | ||
Medical condition: Meteorism symptoms in women dominated by bloating | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001104-41 | Sponsor Protocol Number: ALXN1840-WD-204 | Start Date*: 2020-07-22 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, open-label study to assess copper and molybdenum balance in participants with Wilson disease treated with ALXN1840 | |||||||||||||
Medical condition: Wilson Disease (WD) | |||||||||||||
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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: 2019-000668-27 | Sponsor Protocol Number: MBW-2017-01 | Start Date*: 2019-09-19 |
Sponsor Name:Marta Maia Boscá Watts | ||
Full Title: Pilot Project for the Treatment of Perianal Disease through the Local Injection of Remsima Guided by Ultrasound. Number of cases. | ||
Medical condition: Perianal disease (PD): alteration associated with inflammatory bowel disease (IBD) that includes fissures, ulcers, fistulas or abscesses, and is one of the most difficult aspects of treating IBD. B... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001119-11 | Sponsor Protocol Number: ParvOryx02 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Oryx GmbH & Co KG | |||||||||||||
Full Title: A non-controlled, single arm, open label, Phase II study of intravenous and intratumoral administration of ParvOryx in patients with metastatic, inoperable pancreatic cancer | |||||||||||||
Medical condition: Pancreatic Cancer with at least one hepatic metastasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004724-11 | Sponsor Protocol Number: 294568 | Start Date*: 2014-09-22 |
Sponsor Name:Karolinska Institute | ||
Full Title: Surgical treatment of peri-implantitis with and without systemically adjunctive antibiotics A prospective, open, randomized, three armed, parallel, placebo controlled clinical trial | ||
Medical condition: peri-implantitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000275-36 | Sponsor Protocol Number: CSUB0202 | Start Date*: 2021-04-23 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Prevention of Glucocorticoid induced impairment of bone metabolism – A Randomized, Placebo-Controlled, Single Centre Clinical Trial | ||
Medical condition: Oral glucocorticoid (GC) therapy leads to a rapid and profound effects on bone metabolism.The gut microbiota is involved in regulating bone metabolism.Lactobacillus reuteri (LR) has been shown to h... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
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