- Trials with a EudraCT protocol (142)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
142 result(s) found for: Ketamine.
Displaying page 5 of 8.
EudraCT Number: 2017-002616-13 | Sponsor Protocol Number: Unknown | Start Date*: 2018-03-14 |
Sponsor Name:Maastricht Universitair Medisch Centrum | ||
Full Title: The effect of perioperative intravenous s-ketamine on acute and chronic postoperative craniotomy pain compared to placebo | ||
Medical condition: Post operative craniotomy pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003318-16 | Sponsor Protocol Number: ERASME PACU 001 | Start Date*: 2007-01-23 | |||||||||||
Sponsor Name:ERASME HOSPITAL | |||||||||||||
Full Title: Prise en charge de l'hyperalgésie en salle de soins post-anesthésie: role de la ketamine et de la clonidine | |||||||||||||
Medical condition: Post-operative pain with poor response to intravenous morphine. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013801-33 | Sponsor Protocol Number: 201010 | Start Date*: 2009-10-07 | |||||||||||
Sponsor Name:Steen W. Henneberg, Børnesmerteenheden, Anæstesi afd. 4013, Juliane Marie Centeret, Rigshospitalet | |||||||||||||
Full Title: Nasal administration af sufentanil+ketamin til procedure-relaterede smerter hos børn. | |||||||||||||
Medical condition: Procedure-relaterede smerter hos børn | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007987-40 | Sponsor Protocol Number: KetaminaEsse | Start Date*: 2008-12-29 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | ||||||||||||||||||
Full Title: Low dose intravenous ketamine (S) associated to thoracic epidural analgesia: effects on the post-thoracotomy pain syndrome (PTPS) | ||||||||||||||||||
Medical condition: All patients that will undergo to an elective thoracotomic surgery in the Hospital Maggiore della Carita` of Novara for a 12 months period. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002239-97 | Sponsor Protocol Number: P060402 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Ketamine en association avec une PCA morphine dans le traitement analgésique postopératoire de patients opérés de prothèse totale de hanche (PTH) | |||||||||||||
Medical condition: Patients opérés d'une prothèse totale de hanche | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013110-27 | Sponsor Protocol Number: D2285C00001 | Start Date*: 2009-08-17 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A phase I, multi-centre, double-blind, placebo-controlled parallel group study to assess the pharmacoMRI effects of AZD6765 in male and female patients fulfilling the criteria for Major Depressive ... | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002080-27 | Sponsor Protocol Number: KPS 2008-01 | Start Date*: 2008-08-06 | ||||||||||||||||
Sponsor Name:Greater Glasgow Health Board/University of Glasgow | ||||||||||||||||||
Full Title: A randomised, double-blind controlled trial of ketamine versus placebo in conjunction with best pain management in neuropathic pain in cancer patients | ||||||||||||||||||
Medical condition: Patients who have neuropathic pain related to cancer and/or treatment for cancer (surgical, chemotherapy or radiotherapy) which has resulted in neuropathic pain. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-003716-12 | Sponsor Protocol Number: RHNIA-001-2021 | Start Date*: 2022-08-24 | ||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet | ||||||||||||||||||||||||||||
Full Title: S-ketamine for cortical spreading depolarisation in patients with severe acute brain injury | ||||||||||||||||||||||||||||
Medical condition: Severe acute brain injury caused by aneurysmal subarachnoid hemorrhage, spontaneous intracerebral hemorrhage or traumatic brain injury. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000202-20 | Sponsor Protocol Number: RC-P0041 | Start Date*: 2015-06-22 | |||||||||||||||||||||||||||||||
Sponsor Name:Groupement des Hôpitaux de l’Institut Catholique de Lille (GHICL) | |||||||||||||||||||||||||||||||||
Full Title: Effect and tolerance of ketamine's subcutaneous bolus during painful care, refractory of bedsore, ulcer, vascular wound care in palliative care units. | |||||||||||||||||||||||||||||||||
Medical condition: Patients’ palliative care for bedsores, ulcers or vascular wounds, which are general characteristics of the patient population that will be included: usually elderly, undernourished and of multiple... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000396-14 | Sponsor Protocol Number: 3/006/11 | Start Date*: 2011-06-15 | |||||||||||||||||||||
Sponsor Name:University of Aberdeen [...] | |||||||||||||||||||||||
Full Title: The use of Ketamine as an anaesthetic during electroconvulsive therapy (ECT) for depression: does it improve treatment outcome? | |||||||||||||||||||||||
Medical condition: Depression. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024265-40 | Sponsor Protocol Number: KETA-FAN | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | |||||||||||||
Full Title: Perineural vs systemic N-methyl-D-aspartate (NMDA) receptors antagonism with ketamine as a reverser of peripheral and central sensitization in phantom limb pain | |||||||||||||
Medical condition: Phantom limb pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002518-38 | Sponsor Protocol Number: KETASONE | Start Date*: 2013-07-04 | |||||||||||
Sponsor Name:Hospital Universitari de Girona Dr. Josep Trueta | |||||||||||||
Full Title: KETAMINE AND DEXAMETHASONE IN THE MANAGEMENT OF LOW BACK PAIN DURING ARTHRODESIS | |||||||||||||
Medical condition: Pain in the lumbar arthrodesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003786-14 | Sponsor Protocol Number: AGO/2011/006 | Start Date*: 2011-12-20 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Heeft het toedienen van ketamine of sevoflurane bij kinderen van 0 tot 14 jaar een meerwaarde tijdens het verwijderen van chirurgische thoraxdrains? | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001493-32 | Sponsor Protocol Number: RC 16/07 | Start Date*: 2008-06-09 | |||||||||||
Sponsor Name:ISTITUTO PER L'INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Comparison between two different sedation strategies (propofol versus propofol plus ketamine) in deep sedation managed by non anesthesiologists. | |||||||||||||
Medical condition: Procedural deep sedation (gastrointestinal endoscopy, lumbar puncture, etc) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004489-16 | Sponsor Protocol Number: V3_KET_NEG_SYMPT_SCZ | Start Date*: 2021-11-03 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Psychiatrie und Psychotherapie | ||
Full Title: Ketamine for the treatment of depressive and negative symptoms in patients with schizophrenia: a randomized controlled cross-over pilot study. | ||
Medical condition: Negative and depressive symptoms of schizophrenia according to DSM-5 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000640-21 | Sponsor Protocol Number: KetCRPS-2 | Start Date*: 2021-11-10 |
Sponsor Name:Center for Pain Medicine, Erasmus MC | ||
Full Title: Long-term pain modulation by intravenous esketamine in Complex Regional Pain Syndrome: a non-inferiority study | ||
Medical condition: Complex Regional Pain Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001520-37 | Sponsor Protocol Number: KETECT | Start Date*: 2014-02-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Skåne University Hospital, Malmö | |||||||||||||||||||||||||||||||||
Full Title: Ketamine as an alternative to electroconvulsive therapy for treatment of major depressive disorder | |||||||||||||||||||||||||||||||||
Medical condition: Major depression disorder | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001787-36 | Sponsor Protocol Number: ANA-07113G | Start Date*: 2008-11-13 |
Sponsor Name:Universitätsklinikum Mannheim, Universitätsklinik für Anästhesiologie und Operative Intensivmedizin | ||
Full Title: Verbessert die perioperative Applikation von Esketamin in subanästhetischer Dosierung die postoperative Analgesie? | ||
Medical condition: This trial investigates the use of esketamine in subanesthetic dosages in patients undergoing surgery performed under general anaesthesia particularly with regard to quality of postoperative analge... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
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: 2015-002667-42 | Sponsor Protocol Number: ABR53999 | Start Date*: 2015-09-09 |
Sponsor Name:AMC | ||
Full Title: Sedation with propofol TCI during ERCP: Is the combination with esketamine more effective and safer than with alfentanil (SPEKA): A randomized controlled multicentre trial | ||
Medical condition: Patients undergoing ERCPs under propofol sedation combined with ketamine or alfentanil given by trained anesthesia nurse. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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