- Trials with a EudraCT protocol (353)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
353 result(s) found for: Oxide.
Displaying page 1 of 18.
| EudraCT Number: 2008-004669-24 | Sponsor Protocol Number: 8103 | Start Date*: 2009-01-02 |
| Sponsor Name:Research Innovation Services, University of Nottingham | ||
| Full Title: Nitrous Oxide and Cerebral Autoregulation | ||
| Medical condition: This study is being conducted to evaluate the effects of inhaled concentrations of 20%, 30% and 40% Nitrous Oxide on cerebral autoregulation in healthy volunteers using transcranial doppler ultraso... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000045-40 | Sponsor Protocol Number: Lachgasv1.0 | Start Date*: 2018-03-08 |
| Sponsor Name:Universitair ziekenhuis Brussel | ||
| Full Title: The effects of nitrous oxide on human vision | ||
| Medical condition: effects on vision: - accomodation - visual acuity - binocularity - stereopsis - colour vision - pupil reflex - eye movements | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-007094-23 | Sponsor Protocol Number: Nitrous oxide protocol V5 | Start Date*: 2008-10-09 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Nitrous oxide and cerebral vasodilatation: a dose-response study in healthy volunteers | ||
| Medical condition: The study will be conducted in healthy volunteers. I will evaluate the effects of inhaled concentrations of nitrous oxide, ranging from 0% to 50%, on cerebral blood flow and cerebral vascular tone ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-018181-36 | Sponsor Protocol Number: 09117 | Start Date*: 2010-02-23 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Nitrous Oxide and Functional Magnetic Resonance Imaging to investigate cerebral regional blood flow, cerebral metabolism and neuronal activity. | ||
| Medical condition: This is part of a series of studies investigating the potential therapeutic use of low dose nitrous oxide in the treatment of cerebral vasospasm, a condition which occurs following brain injury and... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022874-15 | Sponsor Protocol Number: 10084 | Start Date*: 2010-11-08 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Comparison of 30% nitrous oxide with therapeutic dose nimodipine on cerebral and systemic vascular physiology | ||
| Medical condition: This is part of a series of studies investigating the potential therapeutic use of low dose nitrous oxide in the treatment of cerebral vasospasm, a condition which occurs following brain injury and... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003242-20 | Sponsor Protocol Number: p135 | Start Date*: 2023-03-09 |
| Sponsor Name:Maastricht University | ||
| Full Title: Effects of recreational nitrous oxide use on psychomotor functioning related to driving performance | ||
| Medical condition: The impairing effects of recreational nitrous oxide use on psychomotor functioning related to driving performance and its relation to detected concentration in exhaled air | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-001469-42 | Sponsor Protocol Number: 35328 | Start Date*: 2011-06-27 |
| Sponsor Name:Deventer Ziekenhuis | ||
| Full Title: A randomised clinical trial on the effectiveness of MediHoney barrier cream versus the standard therapy with zinc oxide in the treatment of intertrigo. | ||
| Medical condition: intertrigo | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023529-39 | Sponsor Protocol Number: RHM CHI 0548 | Start Date*: 2011-02-18 |
| Sponsor Name:Southampton University Hopsitals NHS Trust | ||
| Full Title: Reducing antibiotic tolerance using low dose nitric oxide in cystic fibrosis – a phase 2 pilot study | ||
| Medical condition: Cystic Fibrosis | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000326-24 | Sponsor Protocol Number: INOT41 | Start Date*: 2005-10-27 | |||||||||||
| Sponsor Name:INO Therapeutics | |||||||||||||
| Full Title: The Effects of Nitric Oxide for Inhalation during Left Ventricular Assist Device (LVAD) Implantation. | |||||||||||||
| Medical condition: Acute right ventricular failure. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000625-30 | Sponsor Protocol Number: INOT22 | Start Date*: 2004-07-21 |
| Sponsor Name:INO Therapeutics | ||
| Full Title: Comparison of Supplemental Oxygen and Nitric Oxide for Inhalation Plus Oxygen in the Evaluation of the Reactivity of the Pulmonary Vasculature During Acute Pulmonary Vasodilator Testing | ||
| Medical condition: : Nitric Oxide for inhalation at 800ppm, plus 100% O2, to be used to assess pulmonary vaso reactivity during Pulmonary Vasodilator Testing | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005678-61 | Sponsor Protocol Number: ESNOD-01 | Start Date*: 2006-02-22 |
| Sponsor Name:University Hospital Tuebingen | ||
| Full Title: Entwicklung einer Untersuchungsmethode zur Bestimmung des NO-Transferfaktors der Lunge Evaluierung der Methode und Normwerterhebung an gesunden Probanden (Development of a new method for steady-sta... | ||
| Medical condition: Lung function testing (NO- and CO Transferfactor) in healthy subjects | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-001677-28 | Sponsor Protocol Number: 2007/08 | Start Date*: 2007-11-28 |
| Sponsor Name:Charité - Universitätsmedizin Berlin | ||
| Full Title: Quantification of the anesthetic effect of nitrous oxide using intravenous "closed-loop" anesthesia | ||
| Medical condition: This is a study of the anesthetic effect of the IMP, nitrous oxide. In this sense "general anesthesia" can be termed the medical condition under investigation. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) FR (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005808-72 | Sponsor Protocol Number: 1266/08 | Start Date*: 2009-09-10 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Effect of preoperatively administered oxycontin and intraoperative nitrous oxide use on remifentanil-induced analgesia | |||||||||||||
| Medical condition: postoperative pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-004928-12 | Sponsor Protocol Number: VICER1 | Start Date*: 2005-03-03 |
| Sponsor Name:INO Therapeutics AB | ||
| Full Title: A pilot, unicenter, prospective, aleatorized, with parallel groups, controlled and open to evaluate the efficacy of the Nitric Oxide for Inhalation in the prevention of reperfusion in pulmonary donor | ||
| Medical condition: pulmonary graft dysfunction | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003287-28 | Sponsor Protocol Number: lustgas 2 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Queen Silvia's Childrens hospital | ||
| Full Title: Nitrous oxide for analgesia and sedation during procedural pain in children -Efficacy ina short and long perspective regarding joint injections | ||
| Medical condition: Juvenile Idiopathic Arthrithis (JIA) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-005426-30 | Sponsor Protocol Number: HISTEROSCOPIA-2013 | Start Date*: 2014-04-10 |
| Sponsor Name:FUNDACION PARA LA INVESTIGACION BIOMEDICA DEL HOSPITAL UNIVERSITARIO PRINCIPE DE ASTURIAS | ||
| Full Title: USE OF NITROUS OXIDE FOR PAIN RELIEF IN DIFFERENT HISTEROSCOPY PROCEDURES | ||
| Medical condition: Pain associated to hysteroscopy procedures | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-013226-17 | Sponsor Protocol Number: AustrNHMRVID436677 | Start Date*: 2009-09-29 |
| Sponsor Name:Plymouth Hospitals NHS Trust | ||
| Full Title: The ENIGMA-II Trial. Nitrous oxide anaesthesia and cardiac morbidity after major surgery: a randomised controlled trial | ||
| Medical condition: The study investigates standard anaesthesia for surgery. There is no single specific 'disease' rather there is a population of patients requiring anaesthesia to permit surgery. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000875-14 | Sponsor Protocol Number: ALS-7-05-A-401 | Start Date*: 2006-07-06 |
| Sponsor Name:AIR LIQUIDE SANTE INTERNATIONAL | ||
| Full Title: Short-, and long-term effects of the intra-operative nitrous oxide administration on the remifentanil-induced post-operative hyperalgesia, morphine consumption and long-term quality of life | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006234-18 | Sponsor Protocol Number: 15277 | Start Date*: 2007-03-26 |
| Sponsor Name:Medisch Centrum Leeuwarden | ||
| Full Title: Treatment of intertrigo: zinc oxide in ketoconazolecream with or without substitution of hydrocortisone | ||
| Medical condition: Patients with intertrigo in the large skin folds as the groin, submammary and axillairy will be included for a medical trial. The intertrigo has to be two-sided, so each patient can be his own cont... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001284-33 | Sponsor Protocol Number: ALS-3-06-P-401 | Start Date*: 2006-06-08 |
| Sponsor Name:air liquide sante international | ||
| Full Title: pain relief management by kalinox 170 bar for short-time painful procedure in paediatric patients "alivio del dolor con kalinox 170 bar en pacientes pediatricos sometidos a procedimientos doloroso... | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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