- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Hemicolectomy.
Displaying page 1 of 1.
EudraCT Number: 2005-000182-19 | Sponsor Protocol Number: CC0401 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Phönix Laboratorium GmbH | |||||||||||||
Full Title: Wirksamkeit und Verträglichkeit von Cholincitrat bei postoperativer Darmatonie nach laparotomischer linksseitiger Hemikolektomie, Sigmaresektion oder Rektumresektion ohne endständiges oder protekti... | |||||||||||||
Medical condition: Postoperative intestinal atony | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000259-33 | Sponsor Protocol Number: 06-AnIt-06 | Start Date*: 2007-08-16 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of Anesthesiology and Intensive Care, University Hospital Münster | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Perioperative protective effects of lidocaine - clinical study on the route and timing of administration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: patients, scheduled for major elective colorectal surgery | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017595-25 | Sponsor Protocol Number: 04-AnIt-09/UKM09_0031 | Start Date*: 2011-02-22 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University Hospital Muenster | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Balanced 6 % HES 130/0.4 vs. balanced crystalloid-based infusion in patients undergoing colorectal surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing colorectal surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002002-43 | Sponsor Protocol Number: INMEPREP-2019 | Start Date*: 2019-12-16 | |||||||||||
Sponsor Name:Fundación Instituto de Investigación Sanitaria Aragón | |||||||||||||
Full Title: Phase IV, unicentric, randomized and open study to confirm the decrease of the incidence of the surgical site infection after elective right hemicolectomy with anterographic mechanical preparation ... | |||||||||||||
Medical condition: Patients undergoing right hemicolectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001561-28 | Sponsor Protocol Number: HES08 | Start Date*: 2008-07-21 |
Sponsor Name:Klinik für Anästhesiologie und Operative Intensivmedizin Klinikum Ludwigshafen | ||
Full Title: Influence of perioperative HES 130/04 adminstration on postoperative complications: A prospective randomized trial in patients undergoing colorectal surgery. | ||
Medical condition: Adult patients (>18 years) of both gender undergoing elective colorectal surgery (hemicolectomy left/right, sigmoid colectomy, rectal resection/amputation) without concomitant resection of liver me... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004746-16 | Sponsor Protocol Number: AMCH06071 | Start Date*: 2006-10-30 |
Sponsor Name:Atrium Medisch Centrum Parkstad | ||
Full Title: Darmvoorbereiding bij linkszijdige colonchirurgie | ||
Medical condition: Bowel preparation for elective left-sided colonic surgery will be investigated. Medical conditions requiring this type of treatment vary, examples are inflammatory and malignant diseases. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006383-29 | Sponsor Protocol Number: MNTX 3301 | Start Date*: 2007-07-06 |
Sponsor Name:Progenics Pharmaceuticals, Inc. | ||
Full Title: A Phase 3, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled Study of Intravenous (IV) Methylnaltrexone Bromide (MNTX) in the treatment of Post-Operative Ileus (POI) | ||
Medical condition: Post Operative ileus (POI) in patients who have had a segmental colectomy via open laparotomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004273-10 | Sponsor Protocol Number: 3200L2-300-WW | Start Date*: 2007-01-08 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. | ||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group study of intravenous Methylnaltrexone (MOA-728) for the treatment of post operative ileus | ||
Medical condition: Post operative ileus (POI) in patients who have had a segmental colectomy via open laparotomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) CZ (Completed) IT (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-005200-96 | Sponsor Protocol Number: ZUH-LAP-HEMI-TQL | Start Date*: 2018-03-09 | |||||||||||||||||||||
Sponsor Name:Associate Professor, Consultant Jens Børglum | |||||||||||||||||||||||
Full Title: Improving perioperative pain management for laparoscopic surgery due to colon cancer using the ultrasound-guided Transmuscular Quadratus Lumborum block. A double blind, randomized, placebo controll... | |||||||||||||||||||||||
Medical condition: Postoperative pain following laparoscopic hemicolectomy or sigmoidectomy due to coloncancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003835-12 | Sponsor Protocol Number: AC17067 | Start Date*: 2018-03-01 | |||||||||||||||||||||
Sponsor Name:The University Of Edinburgh [...] | |||||||||||||||||||||||
Full Title: A placebo controlled randomised trial of intravenous lidocaine in accelerating gastrointestinal recovery after colorectal surgery | |||||||||||||||||||||||
Medical condition: Patients scheduled for elective colorectal resection for colorectal cancer or diverticular disease. | |||||||||||||||||||||||
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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: 2013-005327-16 | Sponsor Protocol Number: | Start Date*: 2014-07-15 | |||||||||||
Sponsor Name:The University of Edinburgh [...] | |||||||||||||
Full Title: A Randomized Open Label Pilot Study to Compare Targinact vs. Oxycodone in Early Return of Gastrointestinal Function after Colorectal Surgery | |||||||||||||
Medical condition: Post-operative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017682-33 | Sponsor Protocol Number: 2009_05/0943 | Start Date*: 2010-03-11 | ||||||||||||||||
Sponsor Name:CHRU de Lille | ||||||||||||||||||
Full Title: L’intérêt de la Xylocaine® et de la kétamine per et postopératoire sur la prise en charge de la douleur postopératoire aigue et chronique après colectomie par Laparoscopie | ||||||||||||||||||
Medical condition: colectomie segmentaire ou totale | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001566-21 | Sponsor Protocol Number: 4767 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:Ismail Gögenur [...] | |||||||||||||
Full Title: Effect of Low-dose Interferon-alfa2a on post-operative immune suppression - a randomized trial | |||||||||||||
Medical condition: Colon cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004567-11 | Sponsor Protocol Number: 75911 | Start Date*: 2020-12-08 | |||||||||||
Sponsor Name:Zealand University Hospital | |||||||||||||
Full Title: Effect of Low-dose Interferon-alfa2a on peri operative immune suppression | |||||||||||||
Medical condition: pMMR Colon cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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