- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Colon perforation.
Displaying page 1 of 1.
EudraCT Number: 2004-000715-26 | Sponsor Protocol Number: BO17920 | Start Date*: 2005-02-02 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A Randomized, Three Arm Multinational Phase III Study to Investigate Bevacizumab (q3w or q2w) in Combination With Either Intermittent Capecitabine Plus Oxaliplatin (XELOX) (q3w) or Fluorouracil/ Le... | |||||||||||||
Medical condition: Adjuvant treatment for patients who have undergone surgery for Colon cancer, AJCC/UICC high-risk Stage II & stage III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) DE (Completed) HU (Completed) GB (Completed) CZ (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001437-14 | Sponsor Protocol Number: IRFMN-CRC-7813 | Start Date*: 2019-09-11 | |||||||||||
Sponsor Name:Associazione Chirurghi Ospedalieri Italiani | |||||||||||||
Full Title: Prophylactic surgery plus hyperthermic intraperitoneal chemotherapy (HIPEC CO2) versus standard surgery in colorectal carcinoma at high risk of peritoneal carcinomatosis. Short and long-term outcom... | |||||||||||||
Medical condition: patients with colorectal carcinoma at high risk peritoneal carcinomatosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000629-32 | Sponsor Protocol Number: MO17092 | Start Date*: 2006-12-21 |
Sponsor Name:University of Oxford | ||
Full Title: Multicentre international study of capecitabine ± bevacizumab as adjuvant treatment of colorectal cancer | ||
Medical condition: adjuvant treatment of colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) AT (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-002169-16 | Sponsor Protocol Number: ERASE-CRC | Start Date*: 2022-06-10 | ||||||||||||||||
Sponsor Name:Fondazione GONO | ||||||||||||||||||
Full Title: EXPLOITING CIRCULATING TUMOUR DNA TO INTENSIFY THE POST-OPERATIVE TREATMENT OF STAGE III AND HIGH-RISK STAGE II RESECTED COLON CANCER PATIENTS WITH ADJUVANT FOLFOXIRI AND/OR POST-ADJUVANT TRIFLURID... | ||||||||||||||||||
Medical condition: STAGE III AND HIGH-RISK STAGE II RESECTED COLON CANCER PATIENTS. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014845-95 | Sponsor Protocol Number: NRL0706-01/2009 (VOM) | Start Date*: 2010-02-22 | |||||||||||
Sponsor Name:Norgine Ltd. | |||||||||||||
Full Title: Open study to assess the tolerability, safety and efficacy of an adapted 2 litre gut cleansing solution (NRL0706) in routine colon cleansing prior to colonoscopies for colon tumour screening | |||||||||||||
Medical condition: Subjects without relevant clinical symptoms for gastrointestinal disorders will undergo a complete selective colonoscopy for colon cancer screening. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002940-17 | Sponsor Protocol Number: N16NCI | Start Date*: 2016-11-25 | |||||||||||
Sponsor Name:Antoni van Leeuwenhoek | |||||||||||||
Full Title: Neoadjuvant immune checkpoint inhibition and novel IO combinations in early-stage colon cancer | |||||||||||||
Medical condition: stage 2-3 adenocarcinoma of the colon | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002562-12 | Sponsor Protocol Number: ENDOS2019 | Start Date*: 2019-09-09 |
Sponsor Name:HOSPITAL GENERAL DE CATALUNYA | ||
Full Title: PRAGMATIC, COMPARATIVE AND RANDOMIZED CLINICAL TRIAL OF THE NEW SOLUTION OF 1 LITER POLYETHYLENE GLYCOL VERSUS SODIUM PICOSULFATE WITH MAGNESIUM CITRATE IN THE EFFECTIVENESS OF SCREENING AND SURVE... | ||
Medical condition: Screening and surveillance colonoscopy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005108-32 | Sponsor Protocol Number: BP29262 | Start Date*: 2014-08-04 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A PHASE II, MULTICENTER, RANDOMIZED, DOUBLE-BLIND STUDY TO EVALUATE THE EFFICACY AND SAFETY OF RO5520985 (VANUCIZUMAB) PLUS FOLFOX VERSUS BEVACIZUMAB PLUS FOLFOX IN PATIENTS WITH PREVIOUSLY UNTREA... | |||||||||||||||||||||||
Medical condition: Patients with cancer of the colon or rectum where the tumor has already spread to other organs(s), | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Prematurely Ended) ES (Completed) IT (Completed) GB (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002586-34 | Sponsor Protocol Number: STEROID_MC_1 | Start Date*: 2020-11-12 | |||||||||||||||||||||||||||||||
Sponsor Name:Department of Anesthesiology, Copenhagen University Hospital Hvidovre, Capital Region of Denmark | |||||||||||||||||||||||||||||||||
Full Title: The effects of preoperative high-dose Dexamethasone on inflammatory response and recovery after emergency laparotomy, a randomized, double-blind, placebo-controlled clinical trial - AHA STEROID ... | |||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing emergency laparotomy due to either Intestinal obstruction or perforated abdominal viscus. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000315-26 | Sponsor Protocol Number: MO18024 | Start Date*: 2004-11-25 |
Sponsor Name:F.Hoffmann-La Roche Ltd. | ||
Full Title: First-line Bevacizumab and Chemotherapy in Metastatic Cancer of the Colon or Rectum. An Expanded Access Program. | ||
Medical condition: Metastatic cancer of the colon or rectum. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) HU (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002209-20 | Sponsor Protocol Number: 2015/222/HP | Start Date*: 2016-08-19 |
Sponsor Name:CHU-Hôpitaux de Rouen | ||
Full Title: PRODIGE 50 - ASPIK : French prospective randomised double blind study on aspirin versus placebo in resected colon cancer with PI3K mutation stage III or II high risk | ||
Medical condition: Mutated PI3K colonic adenocarcinoma patients with surgical resection R0 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015598-11 | Sponsor Protocol Number: IGR2009/1539 | Start Date*: 2010-03-12 | ||||||||||||||||
Sponsor Name:Institut Gustave Roussy | ||||||||||||||||||
Full Title: Essai de phase III multicentrique comparant la surveillance simple (standard) à la laparotomie exploratrice plus chimio-hyperthermie intrapéritonéale (CHIP), chez des patients atteints d’un cancer ... | ||||||||||||||||||
Medical condition: Cancers colorectaux à très haut risque de développer une carcinose péritonéale | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001180-11 | Sponsor Protocol Number: ML20514 | Start Date*: 2009-03-16 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: An Open-label, single-arm, Phase II study to evaluate the efficacy and the feasibility of bevacizumab (Avastin®) based on a FOLFOXIRI regimen until progression in patients with previously untreated... | |||||||||||||
Medical condition: previously untreated metastatic colorectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003957-10 | Sponsor Protocol Number: SCOT-2007-01 | Start Date*: 2011-01-31 | ||||||||||||||||
Sponsor Name:Greater Glasgow Health Board (GGHB)/ University of Glasgow | ||||||||||||||||||
Full Title: Short Course Oncology Therapy - A study of adjuvant chemotherapy in colorectal cancer | ||||||||||||||||||
Medical condition: Colorectal Cancer | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DK (Completed) ES (Completed) SE (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018431-18 | Sponsor Protocol Number: REMICADECRD3001 | Start Date*: 2010-08-23 | |||||||||||
Sponsor Name:Janssen Biologics B.V. | |||||||||||||
Full Title: Prospective, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Comparing REMICADE® (infliximab) and Placebo in the Prevention of Recurrence in Crohn’s Disease Patients Undergoing Surg... | |||||||||||||
Medical condition: Crohn’s disease (CD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) FR (Completed) BE (Completed) NL (Completed) IT (Completed) HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
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