- Trials with a EudraCT protocol (23)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
23 result(s) found for: Esophagectomy.
Displaying page 1 of 2.
EudraCT Number: 2016-001853-41 | Sponsor Protocol Number: 57698 | Start Date*: 2018-09-19 | ||||||||||||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||
Full Title: Intensive endoscopic therapy versus conventional treatment for untreated benign anastomotic strictures after esophagectomy: a pilot and randomized controlled trial | ||||||||||||||||||||||||||||
Medical condition: Benign esophagogastric anastomotic strictures after esophagectomy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003974-33 | Sponsor Protocol Number: CE150171 | Start Date*: 2021-05-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA UDINE | |||||||||||||
Full Title: Thoracic duct identification with indocyanine green fluorescence during esophagectomy | |||||||||||||
Medical condition: Chylothorax is a serious post-operative complication, with occurs in 2-12% of patients undergoing esophagectomy. Thoracic duct lesion leads to a reduction of body fluids and albumin resulting in hy... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004374-25 | Sponsor Protocol Number: 61528 | Start Date*: 2020-03-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA UDINE | |||||||||||||
Full Title: Thoracic duct identification with Indocyanine green fluorescence during minimally invasive esophagectomy with patient in prone position | |||||||||||||
Medical condition: Chylothorax is a serioso post-operative complication, which occurs in 2-12% of patients undergoing esophagectomy. Thoracic duct lesion leads to a reduction of body fluids and albumin resulting in h... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000938-49 | Sponsor Protocol Number: PT026/08/01 | Start Date*: 2008-08-18 |
Sponsor Name:Proteo Biotech AG | ||
Full Title: Placebo-controlled Randomized Trial to evaluate the Effect of Elafin on Cytokine Profiles after Major Surgery - Phase II | ||
Medical condition: Esophagectomy is the surgical removal of all or part of the esophagus. The patients enrolled in the study will undergo this surgery for treatment of esophageal cancer. The condition under investig... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002816-30 | Sponsor Protocol Number: 01072021 | Start Date*: 2021-11-12 | |||||||||||
Sponsor Name:Department of Anaesthesiology, Aarhus University Hospital | |||||||||||||
Full Title: Individualised perioperative blood pressure and fluid therapy in oesophagectomy - Study protocol for a prospective randomised controlled trial | |||||||||||||
Medical condition: Oesophagectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004978-17 | Sponsor Protocol Number: FAR-NP-2017-01 | Start Date*: 2017-07-27 | ||||||||||||||||||||||||||
Sponsor Name:Hospital Universitari Bellvitge | ||||||||||||||||||||||||||||
Full Title: CLINICAL, RANDOMIZED, DOUBLE LIND CLINICAL TRIAL TO STUDY THE EFFECT OF PARENTERAL SUPPLEMENTATION WITH FISH OIL EMULSION IN THE NUTRITIONAL SUPPORT IN ESOPHAGECTOMIZED PATIENTS | ||||||||||||||||||||||||||||
Medical condition: Esophagectomy due to esophageal neoplasia | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001200-38 | Sponsor Protocol Number: OTIS2019_001 | Start Date*: 2020-11-17 | |||||||||||
Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
Full Title: Octreotide treatment to improve nutritional recovery after surgery for patients with esophageal or gastric cancer, a prospective randomized open label phase II study - OTIS | |||||||||||||
Medical condition: Undesired weight loss after operation for esophageal or gastric 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: 2020-000878-15 | Sponsor Protocol Number: NL72398.041.19 | Start Date*: 2020-04-15 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Sentinel node Navigation surgery in early esophageal Adenocarcinoma Patients with lymph node involvement: SNAP-IV study | ||
Medical condition: Esophageal adenocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004689-18 | Sponsor Protocol Number: Bay a 0128/11800 | Start Date*: 2006-06-28 | |||||||||||
Sponsor Name:Bayer Inc. | |||||||||||||
Full Title: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Design, 2-Arm Study to Investigate the Effect of Aprotinin on Transfusion Requirements in Patients Undergoing Surgical Procedu... | |||||||||||||
Medical condition: Thoracic surgery in patient with lung or esophageal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) DK (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001856-12 | Sponsor Protocol Number: NT-12331-5 | Start Date*: 2011-08-11 |
Sponsor Name:The Motol University Hospital | ||
Full Title: Early assessment of effectivness of neoadjuvant chemotherapy for carcinoma of the esophagus and esophago-gastric junction using FDG-PET/CT. | ||
Medical condition: adenocarcinoma of the esophagus and esophago-gastric junction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002147-18 | Sponsor Protocol Number: ABR49503 | Start Date*: 2015-07-02 |
Sponsor Name:Academic Medical Center | ||
Full Title: A randomized controlled double-blinded trial comparing the effect of on Demand ROcuronium boluses vs continuous infusion on rating of surgical and anesthesia conditions and need for reversal in Pat... | ||
Medical condition: oesophageal carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003133-18 | Sponsor Protocol Number: NL.58570.091.16 | Start Date*: 2017-01-19 |
Sponsor Name:radboudumc | ||
Full Title: Preoperative staging by combidex MRI in patients with resectable esophageal carcinoma, a feasibility study | ||
Medical condition: Detection of locoregional lymph node metastases in patients with resectable esophageal carcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005749-10 | Sponsor Protocol Number: NL38212 | Start Date*: 2012-08-01 | ||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||
Full Title: Safety and Feasibility of TachoSil®: Application on Esophageal Anastomoses. A non-randomized single center study. | ||||||||||||||||||
Medical condition: Anastomotic leakage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000355-37 | Sponsor Protocol Number: MEC-2022-0373 | Start Date*: 2022-08-29 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: Nivolumab during active surveillance after neoadjuvant chemoradiation for esophageal cancer: SANO-3 study | ||
Medical condition: Operable patients ≥ 18 years of age with locoregionally advanced squamous cell- or adenocarcinoma of the esophagus or esophagogastric junction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003854-17 | Sponsor Protocol Number: N17PND | Start Date*: 2018-02-14 | ||||||||||||||||
Sponsor Name:Antoni van Leeuwenhoek | ||||||||||||||||||
Full Title: Neoadjuvant capecitabine, oxaliplatin, docetaxel and atezolizumab in non-metastatic, resectable gastric and GE-junction cancer. | ||||||||||||||||||
Medical condition: GE junction cancer, gastric cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003118-26 | Sponsor Protocol Number: RAMSES/FLOT7 | Start Date*: 2016-04-26 | |||||||||||
Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | |||||||||||||
Full Title: RAMSES / FLOT7 Perioperative RAMucirumab in combination with FLOT versus FLOT alone for reSEctable eSophagogastric adenocarcinoma RAMSES - a phase II/III trial of the AIO | |||||||||||||
Medical condition: locally advanced resectable adenocarcinoma of the esophagogastric junction or the stomach | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013259-31 | Sponsor Protocol Number: 6232 | Start Date*: 2009-12-29 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: A multicenter double blind placebo-controlled randomised trial for benign esophageal anastomotic strictures: Savary dilation vs savary dilation with Triamcinolon | ||||||||||||||||||
Medical condition: Patients with first time dysphagia (grade 2-4) due to a benign anastomotic esophageal stricture | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000782-21 | Sponsor Protocol Number: VHIO19001 | Start Date*: 2019-06-25 | |||||||||||
Sponsor Name:Vall d' Hebron Institute of Oncology (VHIO) | |||||||||||||
Full Title: Phase II Study of Avelumab plus chemotherapy in the peri-operative treatment for patients with resectable Gastric cancer (GC) or Gastroesophageal Junction cancer (GEJC) – MONEO Study | |||||||||||||
Medical condition: Resectable Gastric cancer (GC) or Gastroesphageal Junction cancer (GEJC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001313-24 | Sponsor Protocol Number: SUPERADD | Start Date*: 2017-02-13 | ||||||||||||||||||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | ||||||||||||||||||||||||||||
Full Title: SUbstition of PERioperative Albumin Deficiency Disorders | ||||||||||||||||||||||||||||
Medical condition: High risk surgical patients or procedures showing a hypoalbuminemia intraoperatively. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005051-42 | Sponsor Protocol Number: PR016-CLN-pro003 | Start Date*: 2008-03-20 | |||||||||||
Sponsor Name:Protherics Salt Lake City, Inc | |||||||||||||
Full Title: A randomized study of the efficacy and safety of OncoGel™ treatment as an adjunctive therapy to systemic chemotherapy and concurrent external beam radiation prior to surgery in subjects with locali... | |||||||||||||
Medical condition: localized or loco-regional esophageal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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