- Trials with a EudraCT protocol (860)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
860 result(s) found for: Saturation.
Displaying page 1 of 43.
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: 2012-005299-32 | Sponsor Protocol Number: OPHT-110912 | Start Date*: 2013-01-24 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Klinische Pharmakologie | |||||||||||||
Full Title: Effect of breathing 100% oxygen on brain metabolites measured by 7-Tesla MRI | |||||||||||||
Medical condition: brain metabolism | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001889-33 | Sponsor Protocol Number: 1790 | Start Date*: 2007-08-24 | ||||||||||||||||
Sponsor Name:North Bristol NHS Trust | ||||||||||||||||||
Full Title: Does an 8 week course of Ambulatory Oxygen Increase Diffuse Parenchymal Lung Diseases Patients Ability to Perform a 6 Minute Walk Test and/or Improve Patients Perception of Quality of Life as measu... | ||||||||||||||||||
Medical condition: Patients enrolled will have a diagnosis of restrictive lung disease diagnosed by a High Resolution CT scan, reduced gas transfer result (obtained from pulmonary function tests) and low lung volumes... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2008-002792-28 | Sponsor Protocol Number: 1.7 | Start Date*: 2008-08-04 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Differences in maternal temperature and saturation after administration of remifentanil PCA or epidural analgesia during labor | |||||||||||||
Medical condition: laborpain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 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: 2020-001768-27 | Sponsor Protocol Number: P20/07 | Start Date*: 2020-04-27 | |||||||||||
Sponsor Name:CH Versailles | |||||||||||||
Full Title: "STUDY OF THE EFFICIENCY OF NORMAL HUMAN IMMUNOGLOBULINS (IVIG) IN PATIENTS AGED 75 YEARS AND OVER COVID-19 WITH SEVERE ACUTE RESPIRATORY FAILURE" GERONIMO 19 | |||||||||||||
Medical condition: Patients aged 75 years and older with confirmed infection Covid19 and saturation SaO2≤ under 95% O2> 5 L / min disqualified from a care in the ICU | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001849-39 | Sponsor Protocol Number: NETs-C19 | Start Date*: 2020-05-18 |
Sponsor Name:Region Skåne | ||
Full Title: Aerosolized DNase I for the treatment of severe respiratory failure in COVID-19 - a phase 2, randomized controlled trial | ||
Medical condition: SARS-coronavirus-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000804-14 | Sponsor Protocol Number: OPHT-070119 | Start Date*: 2019-05-10 |
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | ||
Full Title: The effect of hyperoxia and hypoxia on fluorescence lifetime imaging ophthalmoscopy in healthy subjects | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001373-33 | Sponsor Protocol Number: 2016-3 | Start Date*: 2017-02-17 |
Sponsor Name:Region Ostergotland | ||
Full Title: Clinical Study Protocol An open phase IV,RCT, evaluating patient controlled sedation, in three different dosages of propofol in healthy subjects undergoing elective gynaecological out-patient su... | ||
Medical condition: Gynecological outpatient surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
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: 2022-001252-41 | Sponsor Protocol Number: NA | Start Date*: 2022-07-08 |
Sponsor Name:CHU de Liège | ||
Full Title: Preventing postoperative anaemia in total knee arthroplasty and impact of intravenous iron supplementation on postoperative functional recovery : a randomized clinical trial | ||
Medical condition: Total Knee Arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001437-12 | Sponsor Protocol Number: COVID-19_ASS | Start Date*: 2020-04-09 | |||||||||||
Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | |||||||||||||
Full Title: Random, controlled, open, one-site clinical trial in adult patients with COVID-19 severe pneumonia treated with immunomodulatory drugs | |||||||||||||
Medical condition: Severe COVID-19 pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2020-002186-34 | Sponsor Protocol Number: MP_COVID19 | Start Date*: 2020-06-03 | |||||||||||
Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR). | |||||||||||||
Full Title: Efficacy of the early use of corticotherapy in CoV-2 infection to prevent the progression of acute respiratory distress syndrome (ARDS) in COVID-19 | |||||||||||||
Medical condition: COVID-19 Pneunomia (SARS-CoV-2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 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: 2015-004380-37 | Sponsor Protocol Number: 0 | Start Date*: 2016-05-03 |
Sponsor Name:University Hospital Sjaelland, Roskilde,Palliative Unit | ||
Full Title: Oral morphine drops for rapid treatment of dyspnea in palliative cancer patients | ||
Medical condition: Morphine drops for palliation of breathlessness in palliative cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
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