- Trials with a EudraCT protocol (79)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
79 result(s) found for: Surgical stress.
Displaying page 1 of 4.
EudraCT Number: 2020-004614-35 | Sponsor Protocol Number: ECO-02 | Start Date*: 2021-11-23 | |||||||||||
Sponsor Name:Ismail Gögenur | |||||||||||||
Full Title: Treatment with SGLT-2 inhibitor for postoperative hyperglycemia in acute abdominal surgery – a randomized trial | |||||||||||||
Medical condition: Postoperative (stress) hyperglycemia in patients with no known diabetes after acute abdominal surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003720-11 | Sponsor Protocol Number: M1084997 | Start Date*: 2006-09-08 | |||||||||||
Sponsor Name:GE Healthcare Finland Oy | |||||||||||||
Full Title: Comparison of the quality of anesthesia and intraoperative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia ... | |||||||||||||
Medical condition: Comparing the intra-operative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia. Back surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000043-40 | Sponsor Protocol Number: GLOBE2017 | Start Date*: 2017-04-24 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: GLP-1 for bridging of hyperglycaemia during cardiac surgery: a randomized controlled trial | |||||||||||||
Medical condition: Hyperglyceamia during Cardiac Surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000874-28 | Sponsor Protocol Number: 1 | Start Date*: 2021-07-08 |
Sponsor Name:Gyn.Dept, Aabenraa Hospital, Sygehus Sønderjylland | ||
Full Title: Effect of 24 mg dexamethasone preoperatively on surgical stress, pain and recovery in robotic-assisted laparoscopic hysterectomy | ||
Medical condition: robotic- assisted hysterectomy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002214-13 | Sponsor Protocol Number: IIBSP-OXI-2013-62 | Start Date*: 2013-10-28 |
Sponsor Name:Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau ? IIB Sant Pau | ||
Full Title: Evaluation of oxidative stress associated with the administration of two different concentrations of oxygen for the maintenance of general anesthesia | ||
Medical condition: General anesthesia and oxidative stress | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011618-12 | Sponsor Protocol Number: a002c | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Helsinki Central university Hospital | |||||||||||||
Full Title: Pharyngeal anaestesia with articaine:does it reduce surgical stress in gastroscopy? | |||||||||||||
Medical condition: Pharyngeal anesthesia for gastroscopy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003088-76 | Sponsor Protocol Number: 11-170 | Start Date*: 2014-07-14 |
Sponsor Name:Clinical Evaluation Research Unit (CERU) | ||
Full Title: SodiUm SeleniTe Adminstration IN Cardiac Surgery surgery (SUSTAIN CSX®-trial) - A randomized controlled trial of high dose sodium-selenite administration in high risk cardiac surgical patients | ||
Medical condition: Selenium is a key component of a number of selenoproteins which protect against oxidative stress and is well recognised for its prominent role in immune defence. Selenoproteins have the potential t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009421-29 | Sponsor Protocol Number: AAA1 | Start Date*: 2009-05-14 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Non - invasive assessment of inflammatory burden in small abdominal aortic aneurysms: A USPIO - enhanced Magnetic Resonance Imaging (MRI) study | |||||||||||||
Medical condition: The thrust of this pilot study is to investigate the utility of USPIO - enhanced MR to image abdominal aortic aneurysms with the aim of highlighting focal areas of inflammation and macrophage infil... | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001693-15 | Sponsor Protocol Number: IPPCollapse-II | Start Date*: 2016-08-08 |
Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
Full Title: Individualized Pneumoperitoneum Pressure in Colorectal laparoscopic surgery versus standard therapy (IPPCollapse II) | ||
Medical condition: Pneumoperitoneum Pressure in Colorectal laparoscopic surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005234-19 | Sponsor Protocol Number: | Start Date*: 2013-10-08 |
Sponsor Name:Blodbanken, Rigshospitalet | ||
Full Title: The effect of prostacyclin on haemostasis as evaluated by thrombelastography and endothelial markers in patients undergoing major abdominal surgery. A pilot study. | ||
Medical condition: Capillary leakage secondary to major surgical stress | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005615-32 | Sponsor Protocol Number: SPIHF-203 | Start Date*: 2016-05-18 |
Sponsor Name:Stealth BioTherapeutics Inc. | ||
Full Title: A Phase 2 Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Effects of 4 Weeks Treatment with Subcutaneous Elamipretide on Left Ventricular Function in Subjects with Stable Heart... | ||
Medical condition: Heart failure with preserved ejection fraction (HFpEF) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001853-25 | Sponsor Protocol Number: 1.2-24.05.2019 | Start Date*: 2019-07-23 |
Sponsor Name:Medical University of Vienna | ||
Full Title: THE USE OF ADV6209 FOR PREMEDICATION IN PAEDIATRIC ANAESTHESIA: A CONTROLLED, RANDOMIZED, DOUBLE BLINDED STUDY | ||
Medical condition: To evaluate the effect of ADV6209, a new oral Midazolam formulation, on preoperative anxiety and sedation levels in paediatric anaesthesia | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003117-11 | Sponsor Protocol Number: BCD101 | Start Date*: 2023-10-24 | |||||||||||
Sponsor Name:Dentlabe s.r.o. | |||||||||||||
Full Title: Study assessing if oxytocin can be used as premedication for anxious patients in dentistry. | |||||||||||||
Medical condition: Premedication in dentistry | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002243-17 | Sponsor Protocol Number: DEXCOM | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:Clínica Universidad de Navarra/Universidad de Navarra | |||||||||||||
Full Title: Conscious sedation for procedures in Dental and Minor Maxillofacial Surgery Unit: optimization of the dexmedetomidine dose (Dexdor®). | |||||||||||||
Medical condition: Sedation for procedures in Dental and Minor Maxillofacial Surgery Unit | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000318-24 | Sponsor Protocol Number: RH-ITA-006 | Start Date*: 2016-08-30 | ||||||||||||||||
Sponsor Name:Dept. of Intensive Care 4131, Copenhagen University Hospital Rigshospitalet | ||||||||||||||||||
Full Title: Stress Ulcer Prophylaxis in the Intensive Care Unit | ||||||||||||||||||
Medical condition: Prophylaxis of stress related gastrointestinal bleeding among critically ill patients in the intensive care unit. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) FI (Completed) NO (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002563-10 | Sponsor Protocol Number: BAY86-4875/15961 | Start Date*: 2013-06-06 |
Sponsor Name:Bayer HealthCare AG | ||
Full Title: Multicenter open-label study to evaluate efficacy of gadobutrol-enhanced cardiac magnetic resonance imaging (CMRI) for detection of significant coronary artery disease (CAD) in subjects with known ... | ||
Medical condition: Subjects with known or suspected Coronary Artery Disease (CAD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001922-26 | Sponsor Protocol Number: BMI-EU-02-008 | Start Date*: 2006-01-06 |
Sponsor Name:Bioheart, Inc | ||
Full Title: A Phase II, Open-label, Randomized, Multicenter Study to Assess the Safety and Cardiovascular Effects of MyoCell™ Implantation by a Catheter Delivery System in Congestive Heart Failure Patients Pos... | ||
Medical condition: Patients with congestive heart failure who have had a previous myocardial infarction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002448-25 | Sponsor Protocol Number: MA3RSTrial | Start Date*: 2012-10-02 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: Magnetic Resonance Imaging Using Ultrasmall Superparamagnetic Particles of Iron Oxide in Patients Under Surveillance for Abdominal Aortic Aneurysms to Predict Rupture or Surgical Repair: the MA3RS ... | |||||||||||||
Medical condition: Abdominal Aortic Aneurysm | |||||||||||||
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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: 2007-002223-32 | Sponsor Protocol Number: E2007-0507 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charité Universitaetsmedizin | ||
Full Title: A multicentre, double-blind, randomised placebo-controlled trial of sodium bicarbonate to prevent acute kidney injury in patients undergoing cardiopulmonary bypass surgery. | ||
Medical condition: Cardiac surgical patients in whom the use of cardiopulmonary bypass is planned and having at least one ore more of the following risk factors for post-operative acute kidney injury • Age ≥ 70 years... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-001069-28 | Sponsor Protocol Number: D5881C00004 | Start Date*: 2015-02-10 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Long-Term Outcomes Study to Assess STatin Residual Risk Reduction with EpaNova in HiGh Cardiovascular Risk PatienTs with Hypertriglyceridemia (STRENGTH) | |||||||||||||
Medical condition: Severe persistent Hypertriglyceridemia in High Cardiovascular Risk Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) EE (Completed) LT (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
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