- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
41 result(s) found for: Gastrointestinal hemorrhage.
Displaying page 1 of 3.
EudraCT Number: 2009-017819-16 | Sponsor Protocol Number: OP-GIB | Start Date*: 2011-08-22 | ||||||||||||||||
Sponsor Name:Juan Cordoba | ||||||||||||||||||
Full Title: Efectos de la administración de ornitina-fenilacetato (OCR-002) en pacientes con cirrosis y hemorragia digestiva alta. Effects of the administration of ornithine phenylacetate (OP, OCR-002) in pati... | ||||||||||||||||||
Medical condition: Hemorragia digestiva en pacientes con cirrosis hepática | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004624-41 | Sponsor Protocol Number: 24092020 | Start Date*: 2021-07-07 | ||||||||||||||||
Sponsor Name:Zealand University Hospital | ||||||||||||||||||
Full Title: Calcium Electroporation for Malignant GI Bleeding – a randomized controlled trial | ||||||||||||||||||
Medical condition: Malignant gastrointestinal bleeding | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015070-35 | Sponsor Protocol Number: RB 09.091 | Start Date*: 2010-05-18 | |||||||||||
Sponsor Name:CHRU de BREST | |||||||||||||
Full Title: Evaluation de l'intérêt d'une préparation de l'intestin Grèle par polyéthylèneglycol pour l'exploration par vidéocapsule endoscopique des saignements digestifs inexpliqués | |||||||||||||
Medical condition: Saignement digestif inexpliqué extériorisé ou non associé à une anémie | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
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: 2007-006102-19 | Sponsor Protocol Number: OM1 | Start Date*: 2008-02-25 | ||||||||||||||||
Sponsor Name:Hospital General Universitario Gregorio Marañón de Madrid | ||||||||||||||||||
Full Title: Tratamiento con omeprazol para la profilaxis de la hemorragia digestiva y el reflujo gastroesofágico en niños críticos Omeprazol treatment for prophylaxis of gastrointestinal bleeding and gastroes... | ||||||||||||||||||
Medical condition: Profilaxis de hemorragia digestiva y prevención del reflujo gastroesofágico en niños críticos | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016716-20 | Sponsor Protocol Number: 08/152/WRI | Start Date*: 2010-03-03 | |||||||||||||||||||||
Sponsor Name:Brighton and Sussex University Hospitals NHS Trust | |||||||||||||||||||||||
Full Title: Better targeting of antidepressants in older people: the influence of age and genetic background on serotonin signalling | |||||||||||||||||||||||
Medical condition: Depression | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000959-14 | Sponsor Protocol Number: 29BRC18.0262 | Start Date*: 2021-03-16 | |||||||||||||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||||||||||||
Full Title: The NIPA study: A randomized double-blind control clinical trial Naloxegol administration to prevent opioids induced gastrointestinal motility disturbance in brain Injured PAtients. | |||||||||||||||||||||||
Medical condition: Prevent opioids induced gastrointestinal motility disturbance in brain Injured Patients. | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024309-11 | Sponsor Protocol Number: ERITRO2011 | Start Date*: 2011-03-16 | |||||||||||
Sponsor Name:JOSEP MARIA BOTARGUES BOTÉ | |||||||||||||
Full Title: Eritromicina versus lavados por sonda nasogástrica para mejorar la calidad visual de la endoscopia digestiva en pacientes con hemorragia digestiva alta. Ensayo clínico aleatorizado | |||||||||||||
Medical condition: HEMORRAGIA DIGESTIVA ALTA | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003339-39 | Sponsor Protocol Number: EHDA-01 | Start Date*: 2017-05-03 | |||||||||||
Sponsor Name:JOSÉ MARÍA PALAZÓN AZORÍN | |||||||||||||
Full Title: A randomized, controlled and double-blind trial of intravenous azithromycin versus intravenous erythromycin as a single dose prior to endoscopy in upper gastrointestinal bleeding | |||||||||||||
Medical condition: Upper gastrointestinal haemorrhage | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005782-12 | Sponsor Protocol Number: P-Monofer-PP-01 | Start Date*: 2013-04-17 | |||||||||||
Sponsor Name:Pharmacosmos A/S | |||||||||||||
Full Title: A, Randomized Comparative, Open-Label Study of Intravenous Iron Isomaltoside 1000 (Monofer®) Administered by High Single Dose Infusions or Standard Medical Care in Women after Postpartum Haemorrhage | |||||||||||||
Medical condition: Postpartum haemorrhage | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002236-87 | Sponsor Protocol Number: RH01561 | Start Date*: 2012-08-16 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | ||||||||||||||||||
Full Title: Clinical Study to Evaluate the Efficacy of Chlorhexidine Mouthwashes | ||||||||||||||||||
Medical condition: Gingival bleeding and gingivitis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000318-24 | Sponsor Protocol Number: RH-ITA-006 | Start Date*: 2016-08-30 | ||||||||||||||||
Sponsor Name:Dept. of Intensive Care 4131, Copenhagen University Hospital Rigshospitalet | ||||||||||||||||||
Full Title: Stress Ulcer Prophylaxis in the Intensive Care Unit | ||||||||||||||||||
Medical condition: Prophylaxis of stress related gastrointestinal bleeding among critically ill patients in the intensive care unit. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) FI (Completed) NO (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005783-10 | Sponsor Protocol Number: P-Monofer-PP-02 | Start Date*: 2013-05-23 | |||||||||||
Sponsor Name:Pharmacosmos A/S | |||||||||||||
Full Title: A Randomized Comparative, Open-Label Study of Intravenous Iron Isomaltoside 1000 (Monofer®) Administered by High Single Dose In-fusions or Red Blood Cell transfusion in Women with Severe Postpar-tu... | |||||||||||||
Medical condition: Severe postpartum anaemia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003168-37 | Sponsor Protocol Number: Thllo | Start Date*: 2019-05-13 |
Sponsor Name:University Tuebingen | ||
Full Title: Therapeutic Iloprost for the treatment of Acute Respiratory Distress Syndrome (ARDS) (the ThIlo-Trial): a prospective, randomized, multicenter phase II study | ||
Medical condition: Acute respiratory distress syndrome requiring mechanical ventilation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001234-17 | Sponsor Protocol Number: A3191084 | Start Date*: 2006-06-15 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: Double-blind, triple dummy, parallel-group, randomized, six-month study to compare celecoxib (200 mg BID) with diclofenac SR (75 mg BID) plus omeprazole (20 mg QD) for gastrointestinal events in su... | |||||||||||||
Medical condition: Treatment of osteoarthritis (OA) and/or rheumatoid arthritis (RA) in high GI risk patients | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) BE (Completed) SE (Completed) CZ (Completed) LT (Completed) DE (Suspended by CA) EE (Completed) PT (Completed) GR (Completed) IE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003315-28 | Sponsor Protocol Number: DR220153 | Start Date*: 2023-02-15 | |||||||||||
Sponsor Name:University of Calgary | |||||||||||||
Full Title: Evaluating oral peri-operative acetylsalicylic acid in subjects undergoing endovascular coiling-only of unruptured brain aneurysms | |||||||||||||
Medical condition: Subjects undergoing elective endovascular coiling-only (primary or balloon-assisted) repair of unruptured brain aneurysms. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003585-40 | Sponsor Protocol Number: NL.TACRO.10.7.19 | Start Date*: 2019-12-17 | |||||||||||
Sponsor Name:St. Antonius Hospital | |||||||||||||
Full Title: An uncontrolled, open label pilot-study assessing the efficacy in reducing bleeding severity, and the safety of oral tacrolimus in patients with hereditary hemorrhagic telangiectasia | |||||||||||||
Medical condition: Gastrointestinal bleeding and epistaxis caused by hereditary hemorrhagic telangiectasia. Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant inherited disease characterized by muco... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002677-19 | Sponsor Protocol Number: IG1605 | Start Date*: 2019-07-24 | |||||||||||
Sponsor Name:Instituto Grifols S.A. | |||||||||||||
Full Title: Pathogenesis of Acute on Chronic Liver Failure (ACLF) and Mechanisms of Action of Plasma Exchange with Human Serum Albumin 5% (PE-A 5%) in Decompensated Cirrhotic Subjects with Systemic Inflammatio... | |||||||||||||
Medical condition: Group 1 and 2: Subjects with cirrhosis with ACLF-1b, ACLF-2, or ACLF-3a detected either at admission or during hospitalization Group 3: Subject with cirrhosis hospitalized for Acute decompensat... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) FR (Completed) AT (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002620-17 | Sponsor Protocol Number: 18-513 | Start Date*: 2019-01-08 | |||||||||||
Sponsor Name:Portola Pharmaceuticals, Inc | |||||||||||||
Full Title: A PHASE 4 RANDOMIZED CLINICAL TRIAL OF ANDEXANET ALFA [ANDEXANET ALFA FOR INJECTION] IN ACUTE INTRACRANIAL HEMORRHAGE IN PATIENTS RECEIVING AN ORAL FACTOR XA INHIBITOR | |||||||||||||
Medical condition: Oral FXa inhibitor-treated patients with acute intracranial bleeding. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) BE (Completed) NL (Completed) ES (Prematurely Ended) GR (Completed) CZ (Completed) LV (Completed) FI (Prematurely Ended) NO (Prematurely Ended) LT (Prematurely Ended) PL (Completed) PT (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003902-14 | Sponsor Protocol Number: EORTC-1741-GITCG | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: DKN-01/atezolizumab as second line treatment of biliarY tract cancer and in combiNAtion or not with paclitaxel as second line treatMent of esophagogastrIC cancer: a multi-center Phase II Trial | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Non-operable biliary tract cancer (BTC) and non-operable esophagogastric cancer (EGC) adenocarcinoma. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: CY (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
