- Trials with a EudraCT protocol (153)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
153 result(s) found for: Respiration.
Displaying page 1 of 8.
EudraCT Number: 2007-002172-34 | Sponsor Protocol Number: ACT6795 | Start Date*: 2007-11-26 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, study evaluating the safety and activity of four escalating single doses of AVE0657 in congestive heart failure patients presenting as Cheyne-Stokes ... | |||||||||||||
Medical condition: Congestive heart failure patients presenting as Cheyne-Stokes Breathing Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005029-31 | Sponsor Protocol Number: P110102 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Under 18 | Gender: | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004973-15 | Sponsor Protocol Number: TETRO | Start Date*: 2018-04-09 | |||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
Full Title: Reversal through TRH of opioid-induced respiratory depression (OIRD) in healthy volunteers | |||||||||||||||||||||||
Medical condition: opioid-induced respiratory depression | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002261-38 | Sponsor Protocol Number: P100504 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001529-88 | Sponsor Protocol Number: LOC 04/2004-01 | Start Date*: 2004-11-08 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Dose efficacy relation of inhalative prostaglandin I2 vs. inhalative prostaglandin E1 in patients with ARDS: comparison of efficacy with respect to paO2/FiO2 ratio, Qs/Qt and PAP. | ||
Medical condition: Patients suffering from ARDS who need in the moment of enrolment artificial respiration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
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: 2016-004072-22 | Sponsor Protocol Number: NINA-1 | Start Date*: 2017-12-07 | |||||||||||||||||||||||||||||||
Sponsor Name:Norwegian University of Science and Technology (NTNU) | |||||||||||||||||||||||||||||||||
Full Title: NTNU Intranasal Naloxone Trial Double blinded, double dummy, randomised controlled trial of intranasal naloxone for pre hospital use | |||||||||||||||||||||||||||||||||
Medical condition: We investigate the reversal of opioid overdoses in the pre hospital setting | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NO (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002512-27 | Sponsor Protocol Number: NL44774.068.13 | Start Date*: 2013-11-25 |
Sponsor Name:Maastricht University | ||
Full Title: The role of bile acids in human brown adipose tissue metabolism | ||
Medical condition: Healthy subjects | ||
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) |
EudraCT Number: 2010-023843-13 | Sponsor Protocol Number: tcr | Start Date*: 2011-04-20 | |||||||||||
Sponsor Name:Hospitalsenheden Horsens [...] | |||||||||||||
Full Title: Dyb sedation med spontan respiration kombineret med lokalanæstesi kontra generel anæstesi til gynækologiske patienter på Dagkirurgisk Center på Regionshospital Horsens. | |||||||||||||
Medical condition: Kvinder der får foretaget en TCRE, TCRF eller TCRP pga blødningsforstyrrelser. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018892-20 | Sponsor Protocol Number: HDZKA-2010-01 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Herz- & Diabeteszentrum NRW | |||||||||||||
Full Title: Pathophysiologie der Cheyne-Stokes Atmung: Senkung des pulmonalkapillären Wedge-Drucks als kausaler Therapieansatz | |||||||||||||
Medical condition: Cheyne-Stokes respiration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014301-14 | Sponsor Protocol Number: 2009-014301-14 | Start Date*: 2009-07-15 | ||||||||||||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||||||||||||
Full Title: Farmacologic prevention with Varenicline in heavy smokers undergoing early detection lung cancer screening | ||||||||||||||||||||||||||||
Medical condition: Heavy smokers with higher risk in developing lung cancer and smoke related diseases | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004583-22 | Sponsor Protocol Number: IDRLS | Start Date*: 2021-06-13 |
Sponsor Name:Medical University of Innsbruck | ||
Full Title: Prospective analysis of the therapeutic efficacy of iron isomaltoside in combination with or without dopaminergic therapy in patients with restless legs syndrome | ||
Medical condition: Restless leg syndorme | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004994-30 | Sponsor Protocol Number: NL68837.091.21 | Start Date*: 2022-02-08 |
Sponsor Name:Roessingh | ||
Full Title: Pulmonary function and sleep related disorders during cervical admission of intrathecal baclofen in spinal cord injury; a safety study | ||
Medical condition: Spasticity in patients with spinal cord injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001824-13 | Sponsor Protocol Number: OXIS | Start Date*: 2022-09-12 | ||||||||||||||||
Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
Full Title: Influence of oxycodone on individuals taking an SSRI | ||||||||||||||||||
Medical condition: Depression | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001978-33 | Sponsor Protocol Number: 150400 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Brighton and Sussex University Hospitals NHS Trust | |||||||||||||
Full Title: How can we optimise inhaled beta2 agonist dose as 'reliever' medicine for wheezy pre-school children? | |||||||||||||
Medical condition: Recurrent wheeze in preschool children | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005802-29 | Sponsor Protocol Number: RD/505/06 | Start Date*: 2007-06-26 | ||||||||||||||||||||||||||
Sponsor Name:Gwent Healthcare NHS Trust | ||||||||||||||||||||||||||||
Full Title: Postoperative analgesia for Total knee replacement: A comparision between intrathecal morphine and peripheral nerve block. | ||||||||||||||||||||||||||||
Medical condition: Postoperative analgesia for Total Knee Replacement | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005365-39 | Sponsor Protocol Number: OR00213 | Start Date*: 2014-03-20 | ||||||||||||||||
Sponsor Name:Research in Real-Life Ltd | ||||||||||||||||||
Full Title: A guideline approach to therapy step-down utilising Flutiform®: change and step-down (FFLU-X study) | ||||||||||||||||||
Medical condition: Asthma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000712-33 | Sponsor Protocol Number: 2008/001 | Start Date*: 2008-05-13 | |||||||||||
Sponsor Name:Medizinische Universität Graz | |||||||||||||
Full Title: Fentanyl for the treatment of dsypnea in patients with chronic heart failure | |||||||||||||
Medical condition: Symptomatic treatment of dyspnea induced by chronic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004851-12 | Sponsor Protocol Number: 06/Q0504/33 | Start Date*: 2008-01-03 | |||||||||||
Sponsor Name:Whittington Hospital NHS Trust | |||||||||||||
Full Title: Prospective randomised cross over comparison on the physiological response to non-invasive ventilation using either Air O2 or Heliox21 | |||||||||||||
Medical condition: Respiratory failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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