- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Richmond Agitation Sedation Scale.
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EudraCT Number: 2022-000943-59 | Sponsor Protocol Number: 280482 | Start Date*: 2022-12-22 | |||||||||||||||||||||
Sponsor Name:Odense University Hospital, anaeshtesiologic intensive ward V | |||||||||||||||||||||||
Full Title: Autonome-nervous system regulated anaesthesia: A randomized controlled trial comparing dexmedetomedine and placebo in heart rate variability monitored children | |||||||||||||||||||||||
Medical condition: Postoperative agitation | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007384-17 | Sponsor Protocol Number: 3005099 | Start Date*: 2009-11-30 | ||||||||||||||||||||||||||
Sponsor Name:Sten Walther | ||||||||||||||||||||||||||||
Full Title: A prospective, multi-centre, randomised, double-blind, placebo-controlled comparison of intravenous dexmedetomidine with haloperidol in treatment of hyperactive delirium after heart surgery. | ||||||||||||||||||||||||||||
Medical condition: Postoperative hyperactive delirium | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005812-24 | Sponsor Protocol Number: MalinJonssonFagerlund10 | Start Date*: 2013-05-02 | ||||||||||||||||
Sponsor Name:Karolinska University Hospital | ||||||||||||||||||
Full Title: Acute ventilatory response to hypoxia during sedation with dexmedetomidine compared to propofol in healthy volunteers. | ||||||||||||||||||
Medical condition: Healthy volunteers and the acute hypoxic ventilatory response during sedation with dexmedetomidine compared to propofol. | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000188-25 | Sponsor Protocol Number: LoveMi | Start Date*: 2013-10-23 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Lormetazepam versus Midazolam used as sedatives for critically ill patients. | ||
Medical condition: Sedation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003385-24 | Sponsor Protocol Number: 2815 | Start Date*: 2016-09-28 |
Sponsor Name:GGZ inGeest, parner VUmc | ||
Full Title: The Recall-study: Rivastigmine for ECT-induced Cognitive Adverse effects in Late Life Depression: a multicenter, randomized, double-blind, placebo-controlled, crossover trial | ||
Medical condition: Interictal delirium during electric convulsive therapy- course | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003225-15 | Sponsor Protocol Number: HALO-ICU | Start Date*: 2017-12-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Comparison between inhaled sedation with Sevoflurane vs endovenous sedation with Propofol in the Intensive Care Unit: a randomized prospective trial | |||||||||||||
Medical condition: Preoperative-scheduled sedation in surgical patients admitted in the Intensive Care Unit (ICU) for postoperative monitoring | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003679-32 | Sponsor Protocol Number: 984 | Start Date*: 2021-11-25 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Erector spinae plane block for reduction of early postoperative pain scores and opioid use in lumbar spinal fusion surgery, a prospective double-blinded randomized placebo controlled trial | ||
Medical condition: Patients planned to undergo elective lumbar spinal fusion surgery with a dorsal surgical approach | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005114-35 | Sponsor Protocol Number: KETAPLAST201300511435 | Start Date*: 2014-04-15 | |||||||||||
Sponsor Name:Helsinki UNiversity Central Hospital [...] | |||||||||||||
Full Title: Administration of S-ketamine for negative pressure wound therapy dressing change associated pain: a randomized, prospective, placebo-controlled cross-over study | |||||||||||||
Medical condition: adult patients undergoing negative pressure wound therapy dressing change | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002418-18 | Sponsor Protocol Number: 2021-10 | Start Date*: 2022-11-09 |
Sponsor Name:University Hospital Tübingen | ||
Full Title: AmaNtadine for NeuroenhancEment in acutE patients Study - A prospective pilot proof of concept phase IIb study in intensive and intermediate care unit patients (ANNES) | ||
Medical condition: Patients on Intermediate Care and Intensive Care Unit (IMC and ICU) with unresponsive wakefulness syndrome not otherwise explained | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004846-28 | Sponsor Protocol Number: NL60118.058.17 | Start Date*: 2018-11-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Efficacy of Sodium Oxybate to promote sleep in the ICU: A randomized controlled trial | ||
Medical condition: Sleep disturbance | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001490-40 | Sponsor Protocol Number: 3005019 | Start Date*: 2012-04-03 | ||||||||||||||||
Sponsor Name:ORION CORPORATION ORION PHARMA | ||||||||||||||||||
Full Title: Comparative evaluation of the effects of dexmedetomidine and propofol on patient/ventilator interaction in difficult-to-wean mechanically ventilated patients; a prospective, open, randomised, mul... | ||||||||||||||||||
Medical condition: Patients requiring mechanical ventilation and sedation in the ICU | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006742-18 | Sponsor Protocol Number: P070106 | Start Date*: 2010-08-25 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Evaluation de l'intérêt de la loxapine dans le contrôle de l'agitation au cours du sevrage de la ventilation mécanique. Etude randomisée, contrôlée. | |||||||||||||
Medical condition: Agitation au cours du sevrage de la ventilation mécanique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001408-41 | Sponsor Protocol Number: UKF-MIT-2020-01 | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:Universitätsklinikum Freiburg | |||||||||||||
Full Title: A prospective, randomized, double blinded placebo-controlled trial to evaluate the efficacy and safety of tocilizumab in patients with severe COVID-19 pneumonia | |||||||||||||
Medical condition: Severe COVID-19 pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004097-15 | Sponsor Protocol Number: GabA-01 | Start Date*: 2015-10-23 |
Sponsor Name:Wilhelminenspital | ||
Full Title: A single center, prospective, randomized, double blind, placebo-controlled, three-way cross-over study of the analgesic effects of Midazolam versus Placebo with Fentanyl as an active control in hum... | ||
Medical condition: nociceptive pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003682-19 | Sponsor Protocol Number: OxyPir1 | Start Date*: 2020-12-18 |
Sponsor Name:UZ Brussel | ||
Full Title: Post-operative patient controlled intravenous oxyco-done vs patient controlled intrav nous piritramide. A randomized controlled trial. | ||
Medical condition: To determine whether oxycodone gives better postoperative pain relief (using VAS scores) than IV piritramide in abdominal and gynecological surgery. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003091-39 | Sponsor Protocol Number: APHP180158 | Start Date*: 2020-02-10 |
Sponsor Name:Assistance Publique des Hôpitaux de Paris | ||
Full Title: To relieve dyspnea with low dose titration of morphine in patients admitted to intensive care for acute respiratory failure: A pilot study - OPIDYS | ||
Medical condition: Adult patients admitted to intensive care for ARI: severe dyspnea (defined by a visual analogue dyspnea scale (EVA-dyspnea) ≥ 40) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001086-32 | Sponsor Protocol Number: 19-001_AMG | Start Date*: 2020-01-02 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: ADVANCE-CSX Pilot – Antioxidant Treatment with Vitamin C in Cardiac Surgery Patients – a Clinical Pilot Study | ||
Medical condition: Patients undergoing high-risk open-heart surgery with the use of cardiopulmonary bypass (CPB) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-001645-12 | Sponsor Protocol Number: ALPHA2PREVENT | Start Date*: 2021-06-28 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Alpha 2 adrenergic receptor agonists for the prevention of delirium and cognitive decline after open heart surgery (ALPHA2PREVENT): randomised controlled trial. | ||
Medical condition: Postoperative delirium and cognitive decline in male and female participants aged 70+ scheduled for open heart surgery | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
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