- 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 11 of 19.
EudraCT Number: 2010-021188-34 | Sponsor Protocol Number: LT2380-PIII-05/10 | Start Date*: 2011-07-01 | |||||||||||||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaine, phenylephrine and tropicamide) for mydriasis and anaesthesia in phacoemulsification cataract surgery | |||||||||||||||||||||||
Medical condition: The aim of this clinical study will be to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) ES (Ongoing) SE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006304-37 | Sponsor Protocol Number: 19.4.324 | Start Date*: 2008-03-19 |
Sponsor Name:NV Organon | ||
Full Title: A multi-center, randomized, parallel-group, active-controlled, safety-assessor blinded trial, comparing the efficacy and safety of 2.0 mg.kg-1 sugammadex with 50 μg.kg-1 neostigmine administered at... | ||
Medical condition: Not applicable | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002294-29 | Sponsor Protocol Number: FIBHGM-ECNC003-2011 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Gregorio Marañon | |||||||||||||
Full Title: STUDY OF PULMONARY AND SYSTEMIC INFLAMMATORY RESPONSE SECONDARY TO PULMONARY RESECTION SURGERY USING INTRAVENOUS ANESTHESIA VERSUS INHALATION ANESTHESIA WITH HALOGENATED AGENTS | |||||||||||||
Medical condition: patients undergoing Lung resection surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000229-35 | Sponsor Protocol Number: 2015/01 | Start Date*: 2016-11-03 |
Sponsor Name:Beaumont Hospital | ||
Full Title: A prospective randomised control trial comparing local anaesthetic subcutaneous wound injection versus local anaesthetic wound percolation in distal forearm fractures | ||
Medical condition: Fracture of distal radius or ulna | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003789-25 | Sponsor Protocol Number: mela1 | Start Date*: 2015-02-26 | |||||||||||
Sponsor Name:Department of surgery, Herlev Hospital | |||||||||||||
Full Title: The anxiolytic effects of melatonin: A randomized, placebo-controlled, double-blinded clinical study. | |||||||||||||
Medical condition: We intend to investigate the anxiolytic effects of melatonin in relation to surgery. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000429-28 | Sponsor Protocol Number: ADJUNCT-2-2021 | Start Date*: 2021-04-21 | |||||||||||
Sponsor Name:Zealand University Hospital, Department of Anaesthesiology | |||||||||||||
Full Title: Combined intravenous dexamethasone and dexmedetomidine as adjuncts to popliteal and saphenous nerve blocks in patients undergoing orthopaedic surgery of the foot and ankle. A randomised, blinded, p... | |||||||||||||
Medical condition: Participants undergoing osseous surgery of the foot or ankle with a popliteal and saphenous nerve blocks as means of providing anagelsia with general anaesthesia will be investigated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020677-17 | Sponsor Protocol Number: ALMED-09-C3-026 | Start Date*: 2011-11-16 | |||||||||||
Sponsor Name:Air Liquide Santé International | |||||||||||||
Full Title: Efficacy and safety of xenon anaesthesia compared to sevoflurane anaesthesia and total intravenous anaesthesia for on-pump coronary artery bypass graft surgery: a randomised, three-arm, single-blin... | |||||||||||||
Medical condition: General anesthesia for on pump coronary artery bypass surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000381-11 | Sponsor Protocol Number: NL42823.018.13 | Start Date*: 2013-05-17 | ||||||||||||||||||||||||||
Sponsor Name:Academisch Medisch Centrum | ||||||||||||||||||||||||||||
Full Title: Paracetamol or NSAID's in acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
Medical condition: acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000436-15 | Sponsor Protocol Number: DD-study-3 | Start Date*: 2015-05-18 | |||||||||||
Sponsor Name:Aarhus Universitet | |||||||||||||
Full Title: Photodynamic diagnosis (PDD) in flexible cystoscopy – a randomized study with focus on significant recurrence | |||||||||||||
Medical condition: Patients with non muscle invasive bladder cancer in their first year after the diagnosis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014568-21 | Sponsor Protocol Number: | Start Date*: 2011-09-07 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: VALIDATION OF AN EFFECT-SITE TARGETED PROPOFOL INFUSION FOR ANAESTHESIA IN CHILDREN | |||||||||||||
Medical condition: Children undergoing general anaesthesia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004479-38 | Sponsor Protocol Number: REG 31/05 | Start Date*: 2006-01-12 |
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | ||
Full Title: Effects of the association remifentanil-propofol in TCI on the respiratory exchanges: comparison between controlled and spontaneous ventilation | ||
Medical condition: general anesthesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006839-51 | Sponsor Protocol Number: AM-KSM-II/4/07 | Start Date*: 2007-10-04 | |||||||||||
Sponsor Name:Dr. Franz Köhler Chemie GmbH | |||||||||||||
Full Title: Physostigmine induced reduction of analgetic treatment (PIRAT trial): Randomisiert kontrollierte Doppelblind-Studie zur analgetischen Wirkung einer postoperativen systemischen Applikation von Physo... | |||||||||||||
Medical condition: female patients in need of getting an abdominal hysterectomy due to an illness | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019420-31 | Sponsor Protocol Number: no sponser | Start Date*: 2011-04-22 |
Sponsor Name: | ||
Full Title: ‘The influence of MAC values and behaviour of a child on emergence delirium after sevoflurane anaesthesia’ | ||
Medical condition: ‘Emergence delirium’ (ED) is described as a mental disorder during recovery from general anaesthesia. After the introduction of new inhalation anaesthetics such as sevoflurane, this phenomenon agai... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002290-36 | Sponsor Protocol Number: H-1-2011-053 | Start Date*: 2011-08-04 | |||||||||||
Sponsor Name:Multidisciplinary Pain Center 7612, Rigshospitalet | |||||||||||||
Full Title: Hyperbaric Oxygen effect on inflammation by a heat injury model in healthy male volunteers | |||||||||||||
Medical condition: experimental Inflammation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002518-23 | Sponsor Protocol Number: 19.4.316 | Start Date*: 2008-10-16 |
Sponsor Name:NV Organon, part of Schering-Plough Corporation | ||
Full Title: A randomized, safety-assessor blinded trial comparing 4.0 mg.kg-1 sugammadex with placebo in adult subjects scheduled for surgery requiring profound neuromuscular blockade | ||
Medical condition: Not applicable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005334-22 | Sponsor Protocol Number: 347PUNCIOHEMODIALISIS | Start Date*: 2016-05-31 |
Sponsor Name:HOSPITAL DE PALAMÓS | ||
Full Title: CLINICAL TRIAL FOR THE TREATMENT OF PAIN IN HEMODIALYSIS PUNCTURE WITH LIDOCAINE / PRILOCAINE, VERSUS CHLOROETHYL, CROSSOVER RANDOMIZED STUDY | ||
Medical condition: Hemodialysis is the most commonly used therapy for renal replacement being the arteriovenous fistula used for vascular access . Venipuncture in patients causes stress, pain and anxiety. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002251-13 | Sponsor Protocol Number: 24052016 | Start Date*: 2016-11-09 |
Sponsor Name:Oulu university hospital | ||
Full Title: The effect of intravenous single-dose dexamethasone on pain after total knee replacement surgery. | ||
Medical condition: Patients with arthrosis of knee joint needing operative treatment i.e. arthroplasty of knee. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-020152-54 | Sponsor Protocol Number: MOLT-2010-01 | Start Date*: 2010-11-17 | |||||||||||
Sponsor Name:MOLTENI | |||||||||||||
Full Title: Pilot double blind study to assess the efficacy and tolerability of morphine sulphate oral solution (Oramorph) given as add-on therapy in the preventive analgesia (pre-medication) in patients under... | |||||||||||||
Medical condition: Add-on therapy in the preemptive analgesia (pre-medication) in patients undergoing laparascopy cholecistectomy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003168-37 | Sponsor Protocol Number: Thllo | Start Date*: 2019-05-13 |
Sponsor Name:University Tuebingen | ||
Full Title: Therapeutic Iloprost for the treatment of Acute Respiratory Distress Syndrome (ARDS) (the ThIlo-Trial): a prospective, randomized, multicenter phase II study | ||
Medical condition: Acute respiratory distress syndrome requiring mechanical ventilation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-000700-14 | Sponsor Protocol Number: 2 | Start Date*: 2019-07-08 |
Sponsor Name:Medical University Graz | ||
Full Title: Pilot-Study comparing analgosedation concepts during placement of regional anaesthesia with either fentanyl, remifentanil, clonidine, EMLA-Patch or placebo in regard of patient's wellbeing, pain an... | ||
Medical condition: Patient with elective orthopedic surgery that will be administered a regional anaesthesia will be subject of the investigation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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