- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5)
5 result(s) found for: Doxapram.
Displaying page 1 of 1.
EudraCT Number: 2012-001849-41 | Sponsor Protocol Number: DOX-101 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Leids Universitair Medisch Centrum (LUMC) | |||||||||||||
Full Title: Two-part, Randomized, Placebo-controlled, Repeated Stepped Infusion Dose Study of the Pharmacodynamics of Doxapram when Co-administered with Opioids (Protocol – doxapram-101). | |||||||||||||
Medical condition: acute respiratory insufficiency, including such conditions as opioid and anesthetic-induced respiratory depression, post-anesthetic atelectasis, and central apneas (e.g., apnea of prematurity). | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002979-17 | Sponsor Protocol Number: K620 | Start Date*: 2018-12-17 | |||||||||||||||||||||
Sponsor Name:Ruprecht-Karls University Heidelberg Medical Faculty, University Hospital | |||||||||||||||||||||||
Full Title: Use of doxapram as a new antiarrhythmic drug for a specific therapy of atrial fibrillation | |||||||||||||||||||||||
Medical condition: Paroxysmal or persistent, non-valvular, atrial fibrillation | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003666-41 | Sponsor Protocol Number: MEC2020-0078 | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:Erasmus MC University Medical Center | |||||||||||||
Full Title: Doxapram versus placebo in preterm newborns: an international double blinded multicenter randomized controlled trial. | |||||||||||||
Medical condition: Preterm infants are at high risk of respiratory failure due to immaturity of the respiratory system. Respiratory failure is caused by a comprised lung function and impaired control of breathing. Co... | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003873-85 | Sponsor Protocol Number: PCS02 | Start Date*: 2016-04-12 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Doxapram as an Additive to Propofol Sedation in Sedation for ERCP - a Placebo controlled, randomized, double-blinded, prospective study | ||
Medical condition: Respiratory depression caused by propofol sedation during an ERCP procedure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002567-27 | Sponsor Protocol Number: CTU 011 B | Start Date*: 2008-11-04 |
Sponsor Name:RIEMSER Arzneimittel AG | ||
Full Title: CLINICAL PHASE III MULTI-CENTRIC, DOUBLE-BLIND, DOUBLE DUMMY, RANDOMISED STUDY TO COMPARE SAFETY AND EFFICACY OF DOPRAM® (DOXAPRAM HYDROCHLORIDE) TO CAFEINE COOPER (CAFFEINE CITRATE) IN THE TREATME... | ||
Medical condition: Premature infants with a corrected gestational age of 25;0 to 30;6 weeks with a immature central nervous system resulting in frequent apnoeic episodes | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
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