- Trials with a EudraCT protocol (447)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
447 result(s) found for: Abdomen.
Displaying page 1 of 23.
EudraCT Number: 2015-001309-14 | Sponsor Protocol Number: MINDED | Start Date*: 2016-10-20 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Heidelberg | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Comparison of the efficacy of using a human acellular dermis (Epiflex®) against the surgical standard procedure for closing an open abdomen with respect to avoiding ventral hernia. A monocenter, ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: open abdomen | |||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-009426-81 | Sponsor Protocol Number: CIA-GaDo | Start Date*: 2009-11-10 | |||||||||||
Sponsor Name:University Heidelberg | |||||||||||||
Full Title: Contrast-enhanced Imaging of the Abdomen: Gadovist® vs. Dotarem® – Intraindividual comparison of 0.1mmol/kg bw gadoterate meglumine with 0.1mmol/kg bw gadobutrol for dynamic abdominal imaging in pa... | |||||||||||||
Medical condition: patients with suspected focal liver or renal lesions | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014659-59 | Sponsor Protocol Number: SURE | Start Date*: 2010-04-20 | |||||||||||
Sponsor Name:U.O. Terapia Intensiva | |||||||||||||
Full Title: MANAGEMENT OF THE PATIENT WITH ACUTE Abdomen abdominal SURGERY UNDER URGENT: Multicentre randomized PILOT STUDY | |||||||||||||
Medical condition: Patients with acute abdomen in which to proceed is necessary to intervention in regime of urgency. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011207-23 | Sponsor Protocol Number: | Start Date*: 2009-08-05 |
Sponsor Name:Hull and east Yorkshire Hospital NHS Trust [...] | ||
Full Title: A study to Investigate the Effect of Intraperitoneal Levobupivacaine on Post Operative Laparoscopic Pain | ||
Medical condition: Post operative pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002215-42 | Sponsor Protocol Number: 22/13 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
Full Title: Single-blind randomized controlled trial for acute abdomen analgesia in Pediatric Emergency department | |||||||||||||
Medical condition: Analgesia in pediatric acute abdominal pain | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002637-37 | Sponsor Protocol Number: PIPACOPC3CC | Start Date*: 2017-09-06 | |||||||||||
Sponsor Name:Kirurgisk Afdeling A, Odense Universitetshospital | |||||||||||||
Full Title: Adjuvant Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC) in resected high risk colon cancer patients. - The PIPAC-OPC3 CC trial - | |||||||||||||
Medical condition: Recurrence after resection for colon cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000050-32 | Sponsor Protocol Number: GE012-097 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:GE Healthcare Ltd. and its affiliates | |||||||||||||||||||||||
Full Title: A phase 4 randomized, double-blind study comparing patient comfort and safety between iodixanol 320 mg I/ml and iopamidol 370 mg I/ml in patients undergoing contrast-enhanced computed tomographic (... | |||||||||||||||||||||||
Medical condition: Patients undergoing CECT imaging of the abdomen/pelvis as part of their routine medical care. | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002408-34 | Sponsor Protocol Number: Nosponsor | Start Date*: 2011-10-05 | |||||||||||
Sponsor Name:Matti Ristikankare | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000125-76 | Sponsor Protocol Number: 2010-11-30 | Start Date*: 2011-04-06 | |||||||||||
Sponsor Name:Hannu Kokki | |||||||||||||
Full Title: OKSIKODONIN KESKUSHERMOSTOPENETRAATIO EPIDURAALISEN ANNOSTELUN JÄLKEEN | |||||||||||||
Medical condition: Perusterveitä potilaita, jotka tulevat gynekologiseen laparotomiaan. Potilaat eivät ole raskaana eivätkä he imetä. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002699-10 | Sponsor Protocol Number: 80015401 | Start Date*: 2021-01-06 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: High dose Ropivacaine versus moderate dose for quadratus lumborum block as postoperative analgesia after percutaneous nephrolithotomy – a blinded randomized non-inferiority study | |||||||||||||
Medical condition: Postoperative pain | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000436-24 | Sponsor Protocol Number: AGI006-001 | Start Date*: 2005-04-08 | |||||||||||
Sponsor Name:AGI Therapeutics Limtied | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of AGI 006 in the treatment of functional dyspepsia. | |||||||||||||
Medical condition: Functional (Non-ulcer) Dyspepsia (FD; NUD) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014620-36 | Sponsor Protocol Number: Kotoe_2 | Start Date*: 2009-12-17 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Tampere University Hospital | ||||||||||||||||||||||||||||||||||||||
Full Title: Electroencephalogram during increasing and decreasing desflurane concentration | ||||||||||||||||||||||||||||||||||||||
Medical condition: Surgical patients scheduled for elective surgery under general anaesthesia. Otherwise in stable medical condition (ASA status less than 3) | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002724-29 | Sponsor Protocol Number: RC 48/07 | Start Date*: 2011-10-26 | |||||||||||
Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Continuous peritoneal infusion of ropivacaine following laparoscopy for postoperative analgesia in children: a randomized, double-blind, placebo-controlled study. | |||||||||||||
Medical condition: Children aged over 1 year, undergoing elective abdominal laparoscopic surgery. | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002356-16 | Sponsor Protocol Number: SUS2012CMR01 | Start Date*: 2012-11-27 | ||||||||||||||||
Sponsor Name:Stavanger University Hospital | ||||||||||||||||||
Full Title: Pre-emptive local anaesthesia in gynecological laparoscopy. | ||||||||||||||||||
Medical condition: Gynecological patients referred for elective day-care laparoscopic surgery. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: NO (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005692-15 | Sponsor Protocol Number: MP-LAPARO | Start Date*: 2006-02-16 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Evaluation of bio-clinician plus of perisurgery administration of Metilprednisolone MP in high doses in short term in laparotomy and laparoscopic colic surgeryfor neoplastic patology. Prospective... | |||||||||||||
Medical condition: patients undergoing to laproscopic and laparotomic colic surgery | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002762-38 | Sponsor Protocol Number: Clin-AGI001-001 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:AGI Therapeutics Limited | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study of AGI 001 in the treatment of functional dyspepsia | |||||||||||||
Medical condition: Functional (Non-ulcer) Dyspepsia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004074-93 | Sponsor Protocol Number: EP005 | Start Date*: 2005-03-01 |
Sponsor Name:EpiTan Limited | ||
Full Title: A Pilot, Phase II, Open, Controlled Study to Evaluate the Safety, Tolerability and Efficacy of a Subcutaneous Implant of Melanotan in Patients Suffering from Recurrent Polymorphous Light Eruption. | ||
Medical condition: Polymorphous Light Eruption (PMLE) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003431-29 | Sponsor Protocol Number: CBGG492A2216 | Start Date*: 2014-05-27 |
Sponsor Name:Novartis Farma S.p.A. | ||
Full Title: A multicenter medical safety follow-up study for patients with partial onset seizures who received more than 28 days of total exposure to BGG492 in studies CBGG492A2207 and/or CBGG492A2212. | ||
Medical condition: Testing for adrenal cortical adenomas in male and female patients Testing for uterine endometrial stromal sarcromas in all female patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000197-11 | Sponsor Protocol Number: A1501067 | Start Date*: 2017-03-15 |
Sponsor Name:Pfizer Inc. | ||
Full Title: Post Marketing Surveillance Study To Evaluate The Safety And Efficacy Of Vfend® IV | ||
Medical condition: Patients diagnosed as ‘invasive aspergillosis’, ‘serious fungal infections caused by Scedosporium apiospermum (asexual form of Pseudallescheria boydii) and Fusarium spp. including Fusarium solani i... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-005395-40 | Sponsor Protocol Number: NSAP-01 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Barts and The London NHS Trust | |||||||||||||
Full Title: Is Buscopan, paracetamol or a combination of both the most effective analgesia for the treatment of non-specific abdominal pain? | |||||||||||||
Medical condition: Adult subjects attending the emergency department complaining of acute abdominal pain | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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 . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
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. |
Query did not match any studies.