- Trials with a EudraCT protocol (173)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
173 result(s) found for: Arterial oxygen saturation.
Displaying page 1 of 9.
EudraCT Number: 2017-004480-12 | Sponsor Protocol Number: 2017-991 | Start Date*: 2018-01-16 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Restrictive vs. Liberal Oxygen Therapy for Trauma patients. PILOT: The TRAUMOX Trial | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Victims of trauma are often healthy individuals prior to the incident, but acquire numerous complications including sepsis and pulmonary complications as well as long-term complications and dimini... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000556-19 | Sponsor Protocol Number: 6011 | Start Date*: 2021-10-20 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Anaesthesia, Centre of Head and Orthopaedics | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Comparing Restrictive vs. Liberal Oxygen Strategies for Trauma Patients: The TRAUMOX2 Trial | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Victims of trauma are often healthy individuals prior to the incident, but acquire numerous complications including sepsis and pulmonary complications and diminished quality of life after trauma. W... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003687-31 | Sponsor Protocol Number: AGO/2018/005 | Start Date*: 2019-01-31 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Influence of continuous administration of phenylephrine versus dobutamine on spinal oxygen saturation, measured with near-infrared spectroscopy (NIRS). | ||
Medical condition: spinal vasculature spinal oxygen saturation muscle oxygen saturation cerebral oxygen saturation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004557-92 | Sponsor Protocol Number: H-19052662 | Start Date*: 2020-01-21 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Acute effects of Sodium-glucose coTRansporter-2 inhibition on renal OxygeNation and AUTonomic function in type 1 diabetes | |||||||||||||
Medical condition: Type 1 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001387-39 | Sponsor Protocol Number: 1.4 | Start Date*: 2019-03-15 |
Sponsor Name:Thoraxklinik-Heidelberg gGmbH | ||
Full Title: A prospective, randomized, controlled trial to assess the effect of long-term oxygen therapy on 6-minute walking distance, clinical parameters and hemodynamics in patients with pulmonary arterial h... | ||
Medical condition: pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000709-38 | Sponsor Protocol Number: BBR | Start Date*: 2015-10-20 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: Acute Effects of Benzbromaron on the pulmonary circulation | |||||||||||||
Medical condition: Pulmonary arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002498-80 | Sponsor Protocol Number: 06062019 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Mikkel Brabrand | |||||||||||||
Full Title: Will titrated oxygen flow to a peripheral oxygen saturation of 88-92% compared with oxygen flow to a saturation >94% reduce mortality in Chronic Obstructive Pulmonary Disease patients with acute ex... | |||||||||||||
Medical condition: Acute COPD Exacerbation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002774-64 | Sponsor Protocol Number: HP 3.1 | Start Date*: 2007-12-04 |
Sponsor Name:Deutsches Herzzentrum Berlin, Kompetenznetz Angeborene Herzfehler | ||
Full Title: Therapy of PAH – Treatment with Sildenafil in Eisenmenger Patients | ||
Medical condition: Patients with pre-existing congenital heart disease may develop Eisenmenger physiology (EP), characterized by development of pulmonary arterial hypertension and intracardiac right to left shunt. Th... | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001710-32 | Sponsor Protocol Number: 2006-101 | Start Date*: 2006-07-05 |
Sponsor Name:Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet | ||
Full Title: PeRioperative OXygen fraction – effect on surgical site Infection and pulmonary complications after abdominal surgery. (The PROXI-study) | ||
Medical condition: Laparotomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002482-34 | Sponsor Protocol Number: GAM10-10 | Start Date*: 2020-05-21 |
Sponsor Name:Octapharma USA | ||
Full Title: Efficacy and safety of Octagam 10% therapy in COVID-19 patients with severe disease progression | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-006174-97 | Sponsor Protocol Number: BST22006 | Start Date*: 2007-05-02 |
Sponsor Name:University of Oxford, Research Governance & Clinical Trials Office | ||
Full Title: Which oxygen saturation level should we use for very premature infants? A randomised controlled trial (BOOST-II UK) | ||
Medical condition: Respiratory distress of newborn ICD codes P22.0, P22.8, P22.9 | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-004705-26 | Sponsor Protocol Number: CRO529 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Safety and Tolerability of Sildenafil in Patients with Eisenmenger Physiology | |||||||||||||
Medical condition: Eisenmenger Syndrome (pulmonary hypertension due to congenital heart disease) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002834-36 | Sponsor Protocol Number: Retro-001 | Start Date*: 2012-09-13 |
Sponsor Name:UMCG | ||
Full Title: Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ... | ||
Medical condition: ophthalmic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002310-39 | Sponsor Protocol Number: Vasta2019 | Start Date*: 2019-09-23 |
Sponsor Name:Norrtälje Sjukhus, Tiohundra AB | ||
Full Title: VAsopressin and STeroids in addition to Adrenaline in cardiac arrest - a randomized clinical trial | ||
Medical condition: In hospital cardiac arrest | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004144-29 | Sponsor Protocol Number: lbnp_methoxy_fent_2019 | Start Date*: 2020-06-24 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Methoxyflurane and fentanyl in hypovolemia induced by lower body negative pressure in healthy volunteers; A randomized, placebo-controlled crossover study | ||
Medical condition: The study will investigate and compare the responses to experimental hypovolemia of methoxyflurane, fentanyl and placebo (NaCl) using the "lower body negative pressure" (LBNP)-model . | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001662-11 | Sponsor Protocol Number: CINC424J12301 | Start Date*: 2020-05-05 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: Phase 3 randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of ruxolitinib in patients with COVID-19 associated cytokine storm (RUXCOVID) | ||
Medical condition: COVID-19 associated cytokine storm | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005107-13 | Sponsor Protocol Number: 002083935121 | Start Date*: 2015-01-27 |
Sponsor Name:Epsom and St Helier University Hospitals NHS Trust R&D Dpt | ||
Full Title: A pilot study of the use of oral modafinil added to standard care in hypercapnic respiratory failure in COPD | ||
Medical condition: Hypercapnic respiratory failure in COPD | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2013-005209-30 | Sponsor Protocol Number: AGO/2013/013 | Start Date*: 2014-01-07 | ||||||||||||||||
Sponsor Name:Ghent University Hospital | ||||||||||||||||||
Full Title: The effect of Hydroxyethylstarch 6% 130/0.4 in a balanced electrolyte solution (Volulyte®) compared to gelatine (Geloplasma®) on microvascular reactivity and tissue oxygen saturation during haemodi... | ||||||||||||||||||
Medical condition: Patients undergoing elective coronary artery bypass grafting surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001023-32 | Sponsor Protocol Number: RACE_01 | Start Date*: 2022-09-14 |
Sponsor Name:Medical University of Vienna | ||
Full Title: The effect of epinephrine, norepinephrine and phenylephrine on intraoperative hemodynamic performance - a prospective double-blinded, randomized clinical trial | ||
Medical condition: Patients > 45 years of age at-risk for cardiovascular complications undergoing moderate- to high-risk major open abdominal surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021572-29 | Sponsor Protocol Number: AMB114588 | Start Date*: 2010-11-23 | |||||||||||||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Research & Development, Ltd | |||||||||||||||||||||||||||||||||
Full Title: An open-label, long term extension study for treatment of pulmonary arterial hypertension in paediatric patients aged 8 years up to 18 years who have participated in AMB112529 and in whom continued... | |||||||||||||||||||||||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GR (Prematurely Ended) DE (Completed) NL (Ongoing) ES (Completed) HU (Completed) IT (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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