- Trials with a EudraCT protocol (731)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
731 result(s) found for: Gastrointestinal system.
Displaying page 1 of 37.
EudraCT Number: 2011-005136-25 | Sponsor Protocol Number: 2011-10-14 | Start Date*: 2012-01-12 | ||||||||||||||||
Sponsor Name:Matti Eskelinen | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007702-30 | Sponsor Protocol Number: CB-01-12/01 | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name:COSMO TECHNOLOGIES LTD | |||||||||||||
Full Title: Feasibility and safety of Infliximab enema treatment in patients with active left-sided ulcerative colitis. An open-label, non comparative, pilot study. | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002246-33 | Sponsor Protocol Number: HLS03/2008 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Local application of mitomicin C for the treatment of stricturing Crohns disease: a phase III, single-center, randomized clinical trial | |||||||||||||
Medical condition: Stricturing Crohns disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004124-12 | Sponsor Protocol Number: 55730 | Start Date*: 2005-05-23 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | |||||||||||||
Full Title: LACTOBACILLUS REUTERI REUTERIN AS A THERAPEUTIC AGENT IN INFANTILE COLIC A PROSPECTIVE STUDY. | |||||||||||||
Medical condition: TREATMENT OF INFANTILE COLIC IN BREASTFED INFANTS OF AGE BETWEEN 21 AND 90 DAYS | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002527-14 | Sponsor Protocol Number: TARGET | Start Date*: 2005-07-01 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: PREDICTIVE PERFORMANCE OF ''TARGET CONTROLLED INFUSION'' OF PROPOFOL ASSOCIATED WITH NEUROPHISIOLOGIC MONITORING WITH BISPECTRAL INDEX AND CEREBRAL STATE INDEX IN PATIENT WITH ELEVATED ANESTESIOLOG... | |||||||||||||
Medical condition: ANAESTESIOLGY IN ASA III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019379-31 | Sponsor Protocol Number: LIVERONE | Start Date*: 2010-03-23 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: Evaluation of epatic rigeneration after G-CSF administartion in patients undergoing embolization procedure or portal vein tying forecasting resective surgery for neoplasia. | |||||||||||||
Medical condition: patients affected by colangiocarcinoma or hepatic metastasis for colon-rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001928-12 | Sponsor Protocol Number: 17/2007/U/Sper | Start Date*: 2007-04-23 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Contrast enhanced ultrasonography effectiveness in early evaluating of the response to the Sunitinib in the patients with advanced GIST. A pilot study | |||||||||||||
Medical condition: Gastrointestinal stromal tumor (GIST) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003192-19 | Sponsor Protocol Number: ISRCTN11225767 | Start Date*: 2013-02-22 | |||||||||||
Sponsor Name:London School Of Hygiene and Tropical Medicine | |||||||||||||
Full Title: Tranexamic acid for the treatment of gastrointestinal haemorrhage: an international randomised, double blind placebo controlled trial | |||||||||||||
Medical condition: Gastrointestinal hemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) RO (Completed) ES (Prematurely Ended) IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003687-10 | Sponsor Protocol Number: NALUGStrial | Start Date*: 2022-01-26 | ||||||||||||||||
Sponsor Name:UZLeuven | ||||||||||||||||||
Full Title: Naloxegol for improving upper gastrointestinal symptoms and gastric emptying rate in patients with opioid induced constipation | ||||||||||||||||||
Medical condition: Opioid induced gastrointestinal dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004127-38 | Sponsor Protocol Number: TILATT/0708 | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE POLICLINICO CONSORZIALE | |||||||||||||
Full Title: USE OF ORAL TILACTASE ENZYMES IN SUBJECTS WITH LACTOSE MALABSORPTION AND INTOLERANCE. CLINICAL RELEVANCE IN A POPULATION WITH HIGH PREVALENCE OF LACTASE DEFICIENCY IN SOUTHERN ITALY. | |||||||||||||
Medical condition: primary lactase deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001755-40 | Sponsor Protocol Number: Prop/TCI/2012 | Start Date*: 2012-05-04 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE DI MILANO | |||||||||||||
Full Title: Propofol TCI (Target Controlled Infusion) vs. Fentanyl plus Midazolam for moderate sedation during endoscopy diagnostic procedures: a prospective, double-blind randomized trial. | |||||||||||||
Medical condition: gastrointestinal tract patologies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004168-24 | Sponsor Protocol Number: BETHESDaCD | Start Date*: 2023-12-29 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: Evaluation of the efficacy of topical treatment with budesonide in children with Crohn's disease located in the esophagus and/or stomach and/or duodenum - BETHESDa | |||||||||||||
Medical condition: Crohn's disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005348-92 | Sponsor Protocol Number: PROGASS | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA' GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
Full Title: PROGASS PRucalopride On the GAstreonteric transit in Systemic Sclerosis | |||||||||||||
Medical condition: Sysemic sclerosis with gastroenteric involvement (constipation) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003654-33 | Sponsor Protocol Number: FLORAL-Sb185 | Start Date*: 2016-12-14 | |||||||||||
Sponsor Name:BIOCODEX | |||||||||||||
Full Title: Effects of the probiotic Saccharomyces boulardii CNCM I-745 and the antibiotic Amoxicillin on the gut microbiota of healthy volunteers An open-label, randomized, parallel groups, monocentric study | |||||||||||||
Medical condition: Healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002122-43 | Sponsor Protocol Number: MICI2011-01 | Start Date*: 2011-07-06 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Iron therapy in IBD patients with normal levels of haemoglobin and chronic fatigue | |||||||||||||
Medical condition: patients with IBD and chronic fatigue | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005203-32 | Sponsor Protocol Number: NERONE | Start Date*: 2012-04-17 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: A prospective, multicenter, open-label, patients with non-erosive gastroesophageal reflux disease (NERD) non-responders to therapy with PPIs | |||||||||||||
Medical condition: non-erosive gastroesophageal reflux disease and apparently resistant to medical therapy with proton pump inhibitors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005260-41 | Sponsor Protocol Number: SA652012 | Start Date*: 2016-10-13 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: Efficacy of optimized thiopurine therapy in ulcerative colitis. | |||||||||||||
Medical condition: Ulcerative Colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005693-36 | Sponsor Protocol Number: CodicesponsorCB-17/01/04 | Start Date*: 2012-01-09 | |||||||||||
Sponsor Name:COSMO TECHNOLOGIES LTD | |||||||||||||
Full Title: Intraepithelial neoplasia detection rate after single oral dose of methylene blue MMX modified release tablets administered to patients with long standing ulcerative colitis undergoing colonoscopy | |||||||||||||
Medical condition: Patients affecetd by Long standing ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000420-26 | Sponsor Protocol Number: UC0011 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name: UCB Biopharma SPRL | |||||||||||||
Full Title: A MULTICENTER, SUBJECT-BLIND, INVESTIGATOR-BLIND, RANDOMIZED, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY, SAFETY, TOLERABILITY, AND PHARMACOKINETICS OF AN IV LOADING DOSE FOLLOWED BY SC ADMIN... | |||||||||||||
Medical condition: SEVERE ACTIVE ULCERATIVE COLITIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003958-82 | Sponsor Protocol Number: IOV-CR-001 | Start Date*: 2012-07-16 | |||||||||||
Sponsor Name:ISTITUTO ONCOLOGICO VENETO | |||||||||||||
Full Title: Comparison of three different medicines for bowel cleasing for total colonoscopy. | |||||||||||||
Medical condition: colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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