- Trials with a EudraCT protocol (368)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
368 result(s) found for: General anesthesia.
Displaying page 10 of 19.
EudraCT Number: 2012-000839-54 | Sponsor Protocol Number: SMi-MW-12 | Start Date*: 2012-06-07 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: The effect of late naloxon-infusion on secondary hyperalgesia after a first degree burn injury | |||||||||||||
Medical condition: Induced pain in volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017921-20 | Sponsor Protocol Number: none | Start Date*: 2010-09-16 |
Sponsor Name:Univ. Klinik für Anästhesiologie | ||
Full Title: Influence of Gender on the Plasma-Effect site equilibration time of propofol anesthetic and Cisatracurium Besylate neuromuscular blocking agent. A pilot study. | ||
Medical condition: effect of Gender on Pharmacokinetics of Propofol and cisatracurium | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004931-25 | Sponsor Protocol Number: INDEX | Start Date*: 2021-09-10 | ||||||||||||||||
Sponsor Name:Turku University Hospital | ||||||||||||||||||
Full Title: Intranasal dexmedetomidine pharmacokinetics on patients under general anesthesia | ||||||||||||||||||
Medical condition: Knee osteoarthritis Hip osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001135-20 | Sponsor Protocol Number: Albumin | Start Date*: 2015-04-28 |
Sponsor Name:Södertälje sjukhus AB | ||
Full Title: Volume kinetics for 20% albumin in conscious and anaesthetized humans with and without inflammation. | ||
Medical condition: Healthy adult volunteers, healthy patients undergoing surgery under general anesthesia, and patients in a state of inflammation after having undergone surgery under general anaesthesia (within 24 h... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000537-69 | Sponsor Protocol Number: PROP2% | Start Date*: 2015-09-21 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Real time monitoring of blood propofol concentration | ||
Medical condition: - General anaesthesia - Pharmacokinetics and Pharmacodynamics of Propofol - Inflammatory parameters - Elective thyroid, oncologic breast,ENT or cervical arthrodesis surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002892-12 | Sponsor Protocol Number: CHUB-VASO-IRC | Start Date*: 2022-09-13 | ||||||||||||||||
Sponsor Name:CHU Brugmann | ||||||||||||||||||
Full Title: Comparison of the efficacy of ephedrine versus norepinephrine in the treatment of hypotension occurring after induction of general anesthesia in patients with chronic renal failure: randomized doub... | ||||||||||||||||||
Medical condition: Hypotension occurring post-induction of general anesthesia in patients with chronic renal failure during elective surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000369-37 | Sponsor Protocol Number: NKT102245 | Start Date*: 2005-02-01 |
Sponsor Name:GlaxoSmithKline Group of Companies | ||
Full Title: A multicentre, randomised, double-blind, placebo-controlled, parallel group study to evaluate the safety and efficacy of oral dosing with GW679769 (50 mg or 150 mg) for 3 consecutive days in conjun... | ||
Medical condition: Post Operative Nausea and Vomiting (PONV) Post Discharge Nausea and Vomiting (PDNV) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HU (Completed) GB (Completed) ES (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002009-37 | Sponsor Protocol Number: 0517 | Start Date*: 2017-07-14 | |||||||||||
Sponsor Name:Neuroanæstesiologisk Klinik, RH/Glostrup | |||||||||||||
Full Title: "The effect of Betamethasone gel and NSAID gel lubricated on the laryngeal mask on pain in the throat, hoarseness and cough after anesthesia. " | |||||||||||||
Medical condition: 'Healthy volunteers' (sore throat, hoarseness and cough, consumption of analgesics, postoperative itching, numbness and burning sensation from the throat) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000232-15 | Sponsor Protocol Number: HIDROGEL-014 | Start Date*: 2016-07-13 |
Sponsor Name:Consorcio Hospital General Universitario de Valencia . Servicio de Anestesia , Reanimacion y tto del Dolor | ||
Full Title: Analgesic efficacy of levobupivacaine administered by wet wound dressing for the management split-thickness skin graft donor sites | ||
Medical condition: acute postoperative pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005179-25 | Sponsor Protocol Number: 402-C-326 | Start Date*: 2016-06-10 | |||||||||||
Sponsor Name:Pacira Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of Femoral Nerve Block with EXPAREL for Postsurgical Analgesia in Subjects Un... | |||||||||||||
Medical condition: Total Knee Arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002314-19 | Sponsor Protocol Number: meduniwien_lma_lido_3 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Anesthesiology | |||||||||||||
Full Title: Larynxmaske bei Kindern nach Atemwegsinfekt: Der Effekt topischer Anästhesie mit Lidocain Effect of Lidocain-gel for laryngeal mask lubrification in pediatric patients after acute respiratory disease | |||||||||||||
Medical condition: Acute respiratory diseases are common in pediatric patients scheduled for general anesthesia, and can cause perioperative problems up to 6 weeks after the acute respiratory infection. In the prese... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004833-25 | Sponsor Protocol Number: UNLOCK | Start Date*: 2017-03-29 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar) | ||
Full Title: Synchronous effect of anesthetics on fMRI, EEG and clinical responses. Development of a more precise system for monitoring anesthetic effect. | ||
Medical condition: General anaesthesia in healthy subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004920-40 | Sponsor Protocol Number: AFFECT | Start Date*: 2021-03-22 |
Sponsor Name:Vestre Viken HF | ||
Full Title: Affective effects of pre-surgery opioids (AFFECT): a randomized double-blind controlled trial | ||
Medical condition: Healthy adult surgery patients. Health status ASA1 or ASA2 as categorised by a medical doctor at the hospital based on medical history, physical examination. The American Society of Anesthesiologis... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006006-27 | Sponsor Protocol Number: 0869-219 | Start Date*: 2012-11-05 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: A Phase IIb, Partially-Blinded, Randomized, Active Comparator-Controlled Study to Evaluate the Pharmacokinetics/Pharmacodynamics, Safety, and Tolerability of Aprepitant in Pediatric Patients for th... | |||||||||||||
Medical condition: Post Operative Nausea and Vomiting in surgical patients | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) CZ (Completed) IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001122-17 | Sponsor Protocol Number: ISRCTN12771155 | Start Date*: 2017-11-13 |
Sponsor Name:SILVIA GONZALEZ SANTOS | ||
Full Title: "ANALGESIC EFFICACY OF INTRADURAL MORPHINE VERSUS INTERCOSTAL LEVOBUPIVACAINE IN THE POSTOPERATIVE PERIOD OF MAJOR PULMONARY RESECTION BY VIDEOTHORASCOCOPY" | ||
Medical condition: Control of the pain in surgery of major resection for videotoracoscopia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000663-83 | Sponsor Protocol Number: SM3-ME-13 | Start Date*: 2013-04-19 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: The effect of Adductor-Channel Blockade with high pain responders after reconstruction of the anterior cruciate ligament | |||||||||||||
Medical condition: Patients who will undergo reconstruktion of ligament cruciate ligament. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005086-55 | Sponsor Protocol Number: 2008/PAEDAN/01 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde and University of Glasgow | |||||||||||||
Full Title: Evaluation of propofol TCI anaesthesia in infants age 6m-3y. | |||||||||||||
Medical condition: Children undergoing general anaesthesia | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002848-25 | Sponsor Protocol Number: CN145-010 | Start Date*: 2006-02-28 |
Sponsor Name:Bristol-Myers Squibb SL | ||
Full Title: Protocol Title: A Phase IV, Multi-Center, Randomized, Double-Blind, Placebo- Controlled Study to Evaluate The Analgesic Efficacy And Safety of IV Paracetamol Versus Placebo in subjects with postope... | ||
Medical condition: Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001215-24 | Sponsor Protocol Number: 7-190320 | Start Date*: 2020-05-12 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The effect of subpectineal obturator nerve block on opioid consumption and pain after hip arthroscopy A double-blind randomized, controlled trial | |||||||||||||
Medical condition: Postoperative pain after hip arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000164-93 | Sponsor Protocol Number: 1000000 | Start Date*: 2006-05-10 |
Sponsor Name:Department of Anesthesiology University Hospital Center | ||
Full Title: Effect of Nutritional Support on Liver Integrity during General Anesthesia for Laparoscopic Cholecystectomy. A Pilot Study | ||
Medical condition: To the best of our knowledge, there is no clinical study on the protective effect of nutritional support on the liver in the perioperative setting using clinical and biological variables. Regarding... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
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