- Trials with a EudraCT protocol (116)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
116 result(s) found for: Gases.
Displaying page 1 of 6.
| EudraCT Number: 2020-003579-16 | Sponsor Protocol Number: BIOMIN | Start Date*: 2021-04-07 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:BIOMIN, a. s. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Multicenter, randomized, 52-week trial to determine the efficacy, adherence, safety, and tolerability of natural calcium and vitamin D3 and vitamin K2 supplementation, respectively, in postmenopaus... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Osteopenia | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: SK (Completed) CZ (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2005-001870-29 | Sponsor Protocol Number: 205.324 | Start Date*: 2005-08-29 |
| Sponsor Name:Hospital Clínic de Barcelona | ||
| Full Title: EFECTOS DE UN ANTICOLINÉRGICO DE ACCIÓN PROLONGADA (BROMURO DE TIOTROPIO) SOBRE EL DESEQUILIBRIO DE LAS RELACIONES VENTILACIÓN-PERFUSIÓN (VA/Q) EN LA ENFERMEDAD PULMONAR OBSTRUCTIVA CRÓNICA ESTABLE | ||
| Medical condition: enfermedad pulmonar obstructiva crónica | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005519-34 | Sponsor Protocol Number: ENVARUS | Start Date*: 2016-02-29 | |||||||||||
| Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | |||||||||||||
| Full Title: Phase II, open, one-site, pilot Clinical trial for assessing the pharmacokinetic characteristics, safety and tolerability after conversion of the immuno-suppressive regimen with Advagraf® to Envars... | |||||||||||||
| Medical condition: Lung transplant stable | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001126-21 | Sponsor Protocol Number: 100423 | Start Date*: 2021-04-14 |
| Sponsor Name:Division of Thoracic and Hyperbaric Surgery, Medical University Graz | ||
| Full Title: Hyperbaric Oxygenation for patients with post-COVID-19 sequelae. Pilot study. | ||
| Medical condition: Multiorgan symptoms after COVID-19 infection (Long COVID) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005410-21 | Sponsor Protocol Number: RAE03 | Start Date*: 2006-04-20 |
| Sponsor Name:Bradford Teaching Hospitals NHS Foundation Trust | ||
| Full Title: Improving the Patient's Experience of a Bone Marrow Biopsy - An evidence based approach to service improvement. | ||
| Medical condition: Procedural pain experienced during bone marrow biopsy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023958-36 | Sponsor Protocol Number: 2011_HV_M2 | Start Date*: 2011-09-02 | ||||||||||||||||
| Sponsor Name:Mª Antònia Perelló Juan | ||||||||||||||||||
| Full Title: Ensayo clínico aleatorizado de fase IV, en secuencia cruzada, doble ciego, comparando la influencia de la flora intestinal productora del gas metano en la respuesta al tratamiento del estreñimiento... | ||||||||||||||||||
| Medical condition: Estreñimiento crónico funcional | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-024657-36 | Sponsor Protocol Number: DSR-01 | Start Date*: 2011-05-17 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Statens Serum Institut | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Metronidazol for the treatment of dientamoebiasis in children in Denmark – A randomized, placebo-controlled, double-blinded clinical trial. | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Presumed symptomatic gastrointestinal infection with the protozoan Dientamoeba fragilis. | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2022-004166-37 | Sponsor Protocol Number: 100424 | Start Date*: 2023-05-02 |
| Sponsor Name:Division of Thoracic and Hyperbaric Surgery, Medical University Graz | ||
| Full Title: Hyperbaric oxygenation for patients with orthostatic dysregulation (postural orthostatic tachycardia) in Long- COVID. Prospectively randomized cross- over study. | ||
| Medical condition: Multiorgan symptoms after COVID-19 infection (Long COVID) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| 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: 2015-002210-71 | Sponsor Protocol Number: 38RC15.154 | Start Date*: 2015-07-01 |
| Sponsor Name:University Hospital Grenoble | ||
| Full Title: Impact of dexmedetomidine on preventive noninvasive ventilation in thoracic trauma | ||
| Medical condition: Thoracic trauma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004890-26 | Sponsor Protocol Number: R0115 | Start Date*: 2005-01-07 |
| Sponsor Name:HULL AND EAST YORKSHIRE NHS TRUST | ||
| Full Title: RANDOMISED CONTROLLED TRIAL OF SEDATION FOR COLONOSCOPY-ENTONOX VERSUS MIDAZOLAM/ FENTANYL | ||
| Medical condition: COLONOSCOPY | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003887-48 | Sponsor Protocol Number: R0239 | Start Date*: 2005-12-21 |
| Sponsor Name:HULL AND EAST YORKSHIRE NHS TRUST | ||
| Full Title: Randomised Controlled Trial of patient-controlled sedation for colonoscopy: Entonox versus target-controlled infusion of propofol | ||
| Medical condition: COLONOSCOPY- NO SPECIFIC MEDICAL CONDITION | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000992-12 | Sponsor Protocol Number: HIPP-CABG | Start Date*: 2008-03-27 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Organ protection by noble gases – A clinical study to investigate Helium induced Pre- and Postconditioning in patients undergoing coronary artery bypass surgery (HIPP-CABG). | ||
| Medical condition: patients undergoing coronary artery bypass surgery, helium induced pre- and postconditioning | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-006233-14 | Sponsor Protocol Number: 2007-006233-14 | Start Date*: 2008-01-03 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Organ protection by noble gases – Helium induced Early and Late Preconditioning (HELP) in human endothelium | ||
| Medical condition: healthy volunteers helium induced organ protection | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002745-35 | Sponsor Protocol Number: rum_baclofen2011 | Start Date*: 2011-09-09 | ||||||||||||||||
| Sponsor Name:UZLeuven | ||||||||||||||||||
| Full Title: A placebo controlled trial with Baclofen for the treatment of patients with clinical suspicion of rumination syndrome or esophageal belching | ||||||||||||||||||
| Medical condition: Rumination syndrome and supragastric belching | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2004-001688-23 | Sponsor Protocol Number: NA17598C | Start Date*: 2004-10-27 |
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||
| Full Title: A multicentre, double-blind, placebo-controlled randomized trial of the efficacy, safety and tolerability of 12 months of once daily treatment with 1 mg of RO3300074 in patients with symptomatic em... | ||
| Medical condition: symptomatic emphysema secondary to alpha-1-antitrypsin deficiency | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) GB (Completed) DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004198-41 | Sponsor Protocol Number: UCDCRC/16/003 | Start Date*: 2017-01-27 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: PROPHYLACTIC OROPHARYNGEAL SURFACTANT FOR PRETERM INFANTS: A RANDOMISED TRIAL (THE POPART TRIAL) | |||||||||||||
| Medical condition: Preterm Infants at risk of respiratory distress syndrome | |||||||||||||
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| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) BE (Completed) SE (Completed) CZ (Completed) PT (Completed) NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004858-25 | Sponsor Protocol Number: RF01 | Start Date*: 2007-02-16 |
| Sponsor Name:Royal Free Hampstead NHS Trust | ||
| Full Title: Study to compare maternal cardiovascular stability with different phenylephrine dosing regimens used to maintain baseline systolic blood pressure following a spinal anaesthetic for elective caesare... | ||
| Medical condition: We are studying healthy pregnant women undergoing planned caesarean section under spinal anaesthesia. We are investigating ways of reducing hypotension due to spinal anaesthesia by comparing 3 diff... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2017-001216-11 | Sponsor Protocol Number: FISAN-BOT-2017-01 | Start Date*: 2017-04-25 |
| Sponsor Name:Dra. A. Teresa Calderón Duque | ||
| Full Title: Usefulness of botulinum toxin type A in the treatment of chronic anal fissure | ||
| Medical condition: Chronic anal fissure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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