- Trials with a EudraCT protocol (44)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
44 result(s) found for: Hypnotic.
Displaying page 1 of 3.
EudraCT Number: 2006-003720-11 | Sponsor Protocol Number: M1084997 | Start Date*: 2006-09-08 | |||||||||||
Sponsor Name:GE Healthcare Finland Oy | |||||||||||||
Full Title: Comparison of the quality of anesthesia and intraoperative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia ... | |||||||||||||
Medical condition: Comparing the intra-operative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia. Back surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000406-11 | Sponsor Protocol Number: NL56591.078.16 | Start Date*: 2016-04-14 |
Sponsor Name:Erasmus University Medical Center | ||
Full Title: The influence of electroencephalographic Narcotrend Index™ - guidance of propofol administration on recovery from procedural sedation for gastrointestinal endoscopy in children between 1 and 12 years | ||
Medical condition: There is no specific medical condition under investigation | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000691-94 | Sponsor Protocol Number: CHUBX2014/35 | Start Date*: 2016-01-29 | |||||||||||||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||||||||||||
Full Title: Self-help program for hypnotics withdrawal in insomniac patients: A randomized controlled clinical trial. | |||||||||||||||||||||||
Medical condition: Insomnia Chronic hypnotic users | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003909-26 | Sponsor Protocol Number: BOP-TCI-001 | Start Date*: 2014-02-04 |
Sponsor Name:UMCG | ||
Full Title: Bayesian optimized Propofol Target-Controlled Infusion | ||
Medical condition: Patients requiring general anaesthesia for surgery using propofol and requiring an arterial line for invasive blood pressure monitoring as part of their clinical care. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002824-19 | Sponsor Protocol Number: NA | Start Date*: 2021-08-12 |
Sponsor Name:CHU de Liège | ||
Full Title: Study of the hypnotic and anti-nociceptive components of Magnesium using Electroencephalogram Spectral Entropy and pupillometry during total intravenous general anesthesia : a randomized double-bli... | ||
Medical condition: Total thyroidectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004632-40 | Sponsor Protocol Number: AGO 2005/ANE/propsev | Start Date*: 2005-11-25 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Study on the pharmacodynamic interactions between propofol and sevoflurane during induction of anesthesia. | ||
Medical condition: Anesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000119-25 | Sponsor Protocol Number: MAS-EEG | Start Date*: 2013-07-31 |
Sponsor Name:masimo | ||
Full Title: Study of the cerebral effects of sevoflurane, propofol and remifentanil as measured by the spontaneous electro-encephalogram | ||
Medical condition: We will include 36 healthy volunteers (American Society of Anesthesiologists 1) stratified to age groups and randomized to different sequence of anesthesia regimen. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000420-15 | Sponsor Protocol Number: AKF1919 | Start Date*: 2016-03-24 | |||||||||||
Sponsor Name:Radboud University Medical Centre, department of Psychiatry | |||||||||||||
Full Title: Slow continuous subcutaneous flumazenil infusion for benzodiazepine dependence: a pilot study | |||||||||||||
Medical condition: Patients diagnosed with benzodiazepine dependence with an average daily dose of at least 30 mg of diazepam equivalence. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002122-23 | Sponsor Protocol Number: NL44307.078.13 | Start Date*: 2013-07-11 |
Sponsor Name:Erasmus University Medical Center | ||
Full Title: The influence of electroencephalographic Narcotrend Index™- guidance of of propofol administration on recovery from procedural sedation for gastrointestinal endoscopy in paediatric patients | ||
Medical condition: There is no medical condition which is under investigation. Paediatric patients, scheduled for gastrointestinal endoscopy under procedural sedation are eligible for inclusion. Depth of sedation wil... | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006018-97 | Sponsor Protocol Number: 4305-006 | Start Date*: 2009-01-28 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase IIb, Multicenter, Randomized, Double-Blind Placebo-Controlled, 2-period adaptive Crossover Polysomnography Study to Evaluate the Safety and Efficacy of MK-4305 in Patients With Primary Inso... | |||||||||||||
Medical condition: Primary Insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005194-30 | Sponsor Protocol Number: P-AD337-021 | Start Date*: 2006-06-12 |
Sponsor Name:Arakis Ltd. | ||
Full Title: A multi-centre, randomised, double-blind, placebo controlled, parallel group exploratory study to investigate the efficacy, safety and tolerability of AD 337 in the treatment of fibromyalgia in fem... | ||
Medical condition: Fibromyalgia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002711-25 | Sponsor Protocol Number: 039SC04253 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: DOSE-FINDING STUDY OF TRAZODONE IN THE TREATMENT OF PATIENTS WITH PRIMARY INSOMNIA | |||||||||||||
Medical condition: TREATMENT OF THE INSOMNIA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000584-25 | Sponsor Protocol Number: FLAM01 | Start Date*: 2012-03-29 |
Sponsor Name:UZBrussel | ||
Full Title: Propofol and etomidate. Are they also safe for patients with Brugada-Syndrome? | ||
Medical condition: Patients suspected to have Brugada Syndrome | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001174-25 | Sponsor Protocol Number: PROREMI | Start Date*: 2006-03-13 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: EFFECT OF REMIFENTANIL AND PRPOPOFOL TIMING ADMINISTRATION ON THE DEEPNESS OF HYPNOSIS. | |||||||||||||
Medical condition: PATIENTS UNDERGOING SURGERY WITH LOCOREGIONAL ANAESTHESIA AND SEDATION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000980-33 | Sponsor Protocol Number: 42847922ISM2005 | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Active- and Placebo-Controlled Polysomnography Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42847922 in Subjects with Ins... | |||||||||||||
Medical condition: Insomnia Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005711-10 | Sponsor Protocol Number: OX22-006 | Start Date*: 2007-02-26 | |||||||||||
Sponsor Name:Orexo AB | |||||||||||||
Full Title: A double-blind, randomised, two-period crossover study to evaluate the hypnotic effects and safety of sublingual zolpidem for the treatment of insomnia. | |||||||||||||
Medical condition: Primary insomnia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003689-37 | Sponsor Protocol Number: RC20_0319 | Start Date*: 2020-10-27 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: REmimazolam infusion in the context of Hypnotic Shortage in the Critical care Unit during the pandemic of COVID-19. The non-randomized, non-controlled, pilot, open, mono-centric REHSCU study. | |||||||||||||
Medical condition: general anaesthesia in ICU | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000174-29 | Sponsor Protocol Number: CNS7056-022 | Start Date*: 2018-07-25 | ||||||||||||||||
Sponsor Name:PAION UK Limited | ||||||||||||||||||
Full Title: Phase III confirmatory efficacy and safety trial of remimazolam (CNS7056) compared with propofol for intravenous anaesthesia during elective surgery | ||||||||||||||||||
Medical condition: Induction and maintenance of general anaesthesia (GA) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) GB (Prematurely Ended) NL (Prematurely Ended) FR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001265-18 | Sponsor Protocol Number: LU 02-030 study No. 10403 | Start Date*: 2005-04-05 |
Sponsor Name:H. Lundbeck A/S | ||
Full Title: Protocol title No.10403: A double-blind, randomised, placebo-controlled, parallel-group, Phase III study evaluating the efficacy and safety of gaboxadol 5 mg and 10 mg daily in elderly outpatients ... | ||
Medical condition: Elderly outpatients with primary insomnia, diagnosed according to DSM IV -TR | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001264-45 | Sponsor Protocol Number: LU 02-030 study No. 10402: | Start Date*: 2005-04-06 |
Sponsor Name:H. Lundbeck A/S | ||
Full Title: Protocol title study No. 10402: A 12-month Phase III safety study of gaboxadol 10 mg daily consisting of a 6-month double-blind, randomised, placebo-controlled, parallel-group periodfollowed by a... | ||
Medical condition: Elderly outpatients with primary insomnia, diagnosed according to DSM IV-TR | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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