- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
19 result(s) found for: Colostomy.
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EudraCT Number: 2015-005614-30 | Sponsor Protocol Number: SOAP2016 | Start Date*: 2016-07-07 |
Sponsor Name:Uzsoki Utcai Kórház | ||
Full Title: SOAP Antibiotic prophylaxis trial Systemic versus combined systemic and Oral Antibiotic Prophylaxis in elective colorectal surgery | ||
Medical condition: In colorectal surgery wildely used bowel prep and systemic antibiotic prophylaxis. New data suggest that infective complications can be lowered if beside this regimen oral antibiotic profilaxis is ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
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: 2010-022754-17 | Sponsor Protocol Number: UCL/09/0176 | Start Date*: 2012-08-22 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: Bevacizumab And Combination Chemotherapy in rectal cancer Until Surgery: A Phase II, Multicentre, Open-label, Randomised Study of Neoadjuvant Chemotherapy and Bevacizumab in Patients with MRI defin... | ||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003671-60 | Sponsor Protocol Number: NO-CUT | Start Date*: 2018-04-23 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA AO OSPEDALE NIGUARDA CA' GRANDA | |||||||||||||
Full Title: TOTAL NEOADJUVANT TREATMENT WITHOUT SURGERY FOR LOCALLY ADVANCED RECTAL CANCER: PROSPECTIVE CLINICAL TRIAL TO ASSESS TUMOR COMPLETE RESPONSE, CIRCULATING TUMOR GENETIC AND EPIGENETIC BIOMARKERS, AN... | |||||||||||||
Medical condition: Adenocarcinoma of the medium/lower rectum in Stage II (cT3-4 N0) or Stage III (cT1-4, N1-2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001471-36 | Sponsor Protocol Number: PrimeRT-2018 | Start Date*: 2020-10-05 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Priming the Tumour MicroEnvironment for Effective Treatment with Immunotherapy in Locally Advanced Rectal Cancer: A Phase II trial of Durvulamab in Combination with Extended Neoadjuvant Regimens i... | |||||||||||||
Medical condition: Rectal Cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
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: 2021-005887-24 | Sponsor Protocol Number: GEMCAD-2103//MO44170 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Grupo Español Multidisciplinar de Cáncer Digestivo (GEMCAD) | |||||||||||||
Full Title: Phase II study of Atezolizumab plus Tiraglolumab in combination with chemoradiotherapy in localized squamous cell carcinoma of the anal canal | |||||||||||||
Medical condition: Locallized squamous cell carcinoma of the anal canal in the first-line setting. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002588-23 | Sponsor Protocol Number: 2019/0407/HP | Start Date*: 2023-03-13 | ||||||||||||||||
Sponsor Name:CHU de Rouen | ||||||||||||||||||
Full Title: Neoadjuvant Chemotherapy for Obstructive Colon cancER first Treated by cOlostomy: A randomized phase III trial - COnCERTO (French 01-18) | ||||||||||||||||||
Medical condition: Patients first treated by stoma and requiring chemotherapy for obstructive colon cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006073-24 | Sponsor Protocol Number: CCR2983 | Start Date*: 2008-05-22 | ||||||||||||||||
Sponsor Name:Royal Marsden Hospital | ||||||||||||||||||
Full Title: CINATRA: Chromosomal Instability and Anti-Tubulin Response Assessment: A Phase II Study of Epothilone B in Metastatic Colon Carcinoma in patients with Microsatellite Instability or Chromosomal Inst... | ||||||||||||||||||
Medical condition: Metastatic or locally recurrent colorectal cancer in genetically unselected patients, followed by recruitment of patients selected for microsatellite positive tumours | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004052-20 | Sponsor Protocol Number: CKTO 2005-25R | Start Date*: 2006-11-01 | |||||||||||
Sponsor Name:Koningin Wilhelmina Fonds | |||||||||||||
Full Title: Phase II study of definitive radiochemotherapy for locally advanced squamous cell cancer of the vulva: an efficacy study | |||||||||||||
Medical condition: advanced stage squamous cell cancer of the vulva | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000331-14 | Sponsor Protocol Number: ICORG 05-02/NSABP C-08 | Start Date*: 2005-04-08 |
Sponsor Name:All Ireland Cooperative Oncology Research Group | ||
Full Title: A phase III clinical trial comparing infusional 5-Fluorouracil (5-FU), Leucovorin and Oxaliplatin (mFOLFOX -6) every 2 weeks with Bevacizumab to the same regimen without Bevacizumab for the treatme... | ||
Medical condition: Resected stage II or stage III adenocarcinoma of the colon | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003005-25 | Sponsor Protocol Number: RADIANCE | Start Date*: 2019-12-17 | ||||||||||||||||
Sponsor Name:University Hospital Frankfurt, Goethe University | ||||||||||||||||||
Full Title: Radiochemotherapy +/- Durvalumab for locally-advanced Anal Carcinoma A multicenter, randomized, phase II trial of the German Anal Cancer Study Group | ||||||||||||||||||
Medical condition: anal cancer (UICC-Stage IIB-IIIC, incl. T2>4cm Nany ) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004916-21 | Sponsor Protocol Number: EROS | Start Date*: 2019-07-02 | |||||||||||
Sponsor Name:Karolinska Institute | |||||||||||||
Full Title: Early intervention and recovery of sexual function in men and women after treatment of rectal cancer–a randomized controlled study with tadalafil compared to standard care | |||||||||||||
Medical condition: sexual/ erectile function in women and men after treatment for rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000252-34 | Sponsor Protocol Number: LCD-CDAD-10-07 | Start Date*: 2012-12-06 | |||||||||||
Sponsor Name:Cubist Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blinded, Active-Controlled Study of CB-183,315 in Patients with Clostridium Difficile Associated Diarrhea | |||||||||||||
Medical condition: Clostridium difficile Associated Diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) DE (Completed) CZ (Completed) PL (Completed) ES (Completed) AT (Completed) GB (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023083-40 | Sponsor Protocol Number: SPON830-10 | Start Date*: 2012-03-19 |
Sponsor Name:Cardiff University | ||
Full Title: A Phase II study of neoadjuvant chemotherapy given before SCPRT as treatment for patients with MRI-staged operable rectal cancer at high risk of metastatic relapse | ||
Medical condition: Rectal adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-005129-99 | Sponsor Protocol Number: TA799-013 | Start Date*: 2021-02-10 | |||||||||||
Sponsor Name:VectivBio AG | |||||||||||||
Full Title: A multicenter, open-label, metabolic balance study to evaluate the effects of apraglutide on intestinal absorption in adult subjects with short bowel syndrome, intestinal failure (SBS-IF), and colo... | |||||||||||||
Medical condition: short bowel syndrome, intestinal failure (SBS-IF), colon-in-continuity (CIC) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003337-40 | Sponsor Protocol Number: final version 2.0 | Start Date*: 2006-02-13 |
Sponsor Name:European Group for Blood and Marrow Transplantation (EMBT) | ||
Full Title: Autologous Stem Cell Transplantation for Crohn's Disease ('ASTIC'-Trial: Autologous Stem Cell Transplantation International Crohn's Disease Trial) | ||
Medical condition: Patients with Crohn's disease who have not responded to immunosupressant medication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IT (Ongoing) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001298-27 | Sponsor Protocol Number: 3200L-301-WW | Start Date*: 2007-08-07 |
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 Postoperative Ileus After Ventral Hernia Repair | ||
Medical condition: Post operative ileus (POI). This study will examine the effect of IV MOA-728 versus placebo in shortening the time to return of bowel function in subjects receiving opioid analgesia administered v... | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: HU (Completed) NL (Completed) BE (Completed) IT (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003289-18 | Sponsor Protocol Number: 219369 | Start Date*: 2023-03-10 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||||||||||||||||||
Full Title: A Phase 2, Single-Arm, Open-Label Study with Dostarlimab Monotherapy in Participants with Untreated Stage II/III dMMR/MSI-H Locally Advanced Rectal Cancer | ||||||||||||||||||
Medical condition: Untreated Stage II/III dMMR/MSI-H locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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