- Trials with a EudraCT protocol (96)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
96 result(s) found for: Regional Anesthesia.
Displaying page 1 of 5.
EudraCT Number: 2015-003498-13 | Sponsor Protocol Number: HIP/FUSION#1 | Start Date*: 2016-03-18 | |||||||||||
Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
Full Title: Surgical anesthesia for elective hip surgery - hemodynamic effect of lumbosacral plexus blockade compared to continuous spinal anesthesia | |||||||||||||
Medical condition: No specific medical condition is investigated. The objective of the investigation is to compare two methods for surgical anesthesia for total hip replacement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000846-20 | Sponsor Protocol Number: ANE-INTRA-2013 | Start Date*: 2013-06-24 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Comparison of the effects of bupivacain or levobupivacain on cerebral oxigenation during intradural anesthesia in elderly patients who undergo major orthopaedic surgery for hip replacement | |||||||||||||
Medical condition: Intradural anaesthesia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002769-37 | Sponsor Protocol Number: cervikalblock | Start Date*: 2012-10-23 |
Sponsor Name:UK für Anästhesiologie und allgemeine Intensivmedizin, LKH Salzburg | ||
Full Title: Influence of the concentration of the local anesthetic ropivacaine in the quality of a ultrasound guided block of the regio collis lateralis for carotid endarterectomy: a prospective, randomized an... | ||
Medical condition: Regional anesthesia for carotid endarterectomy surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001657-27 | Sponsor Protocol Number: -- | Start Date*: 2018-10-03 |
Sponsor Name: | ||
Full Title: Comparison of ultrasound guided Serratus Anterior Plane Block (SAPB) with continuous local anesthetic infusion and epidural analgesia in the treatment of multiple rib fracture analgesia: a prospect... | ||
Medical condition: Multiple traumatic rib fractures | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001300-30 | Sponsor Protocol Number: 2017_CERVPLEX_1.1 | Start Date*: 2017-10-03 |
Sponsor Name:UK für Anästhesieologie, Gemeinn. Sbg. Landeskliniken BetriebsgesmbH | ||
Full Title: Comparison of deep, intermediate and superficial cervical plexus block for carotid endarterectomies concerning paresis of the phrenic nerve, lung function and tissue distribution: a prospective, ra... | ||
Medical condition: deep, intermediate or superficial cervical plexus block for carotid endarterectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000314-38 | Sponsor Protocol Number: PSS2018/DEXPED-MEISTELMAN/YB | Start Date*: 2018-09-11 | |||||||||||
Sponsor Name:CHRU de NANCY | |||||||||||||
Full Title: Efficiency of IV dexamethasone compared to placebo, administrated after a lower limb blockade is done, on the post operative pain in children : a controled, randomised, double blind study. | |||||||||||||
Medical condition: post operative pain | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004242-10 | Sponsor Protocol Number: MM1-2020 | Start Date*: 2020-12-21 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Centre for Anaesthesiological Research, Department of Anaesthesiology, Zealand University Hospital, Køge, Denmark | |||||||||||||||||||||||||||||||||||||||||||
Full Title: Does perineural dexamethasone increase the duration of an ulnar nerve block when controlling for systemic effects? A randomised, blinded, placebo-controlled, paired, non-inferiority trial in health... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: We will not assess a specific medical condition or disease as only healthy volunteers are included. We will assess if perineural dexamethasone increases the duration of a peripheral nerve block (i.... | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002399-25 | Sponsor Protocol Number: Sevo-Des-2015-01 | Start Date*: 2015-11-04 |
Sponsor Name:Servicio de Anestesia Infantil. Hospital Universitario La Paz | ||
Full Title: CLINICAL TRIAL TO COMPARE THE INCIDENCE AND CHARACTERISTICS OF POSTOPERATIVE AGITATION IN PEDIATRIC PATIENTS AFTER ANESTHESIA WITH SEVOFLURANE OR DESFLURANE IN AMBULATORY SURGERY. | ||
Medical condition: AGITATION AFTER POSTOPERATIVE ANESTHESIA IN PEDIATRIC PATIENTS | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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 |
EudraCT Number: 2017-001644-35 | Sponsor Protocol Number: CR_TFB_2017 | Start Date*: 2017-06-01 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The effect of popliteal plexus block on pain after total knee replacement | |||||||||||||
Medical condition: In this study we investigate pain after total knee replacement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002325-11 | Sponsor Protocol Number: AT052016 | Start Date*: 2016-07-27 |
Sponsor Name:Univerity Hospital Leuven | ||
Full Title: Intravenous regional anesthesia versus axillar block for hand surgery in day-care hospitall: A prospective, randomised, comparative trial | ||
Medical condition: intra and post operative pain management | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004377-41 | Sponsor Protocol Number: TFP_1-1 | Start Date*: 2016-12-19 | |||||||||||
Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital | |||||||||||||
Full Title: Regional anaesthesia of the cutaneus nerves of the hip - A randomized controlled trial of the transversalis fascia plane block | |||||||||||||
Medical condition: Postoperative pain after hip surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002563-41 | Sponsor Protocol Number: RFCLAI004 | Start Date*: 2016-02-09 | |||||||||||
Sponsor Name:Jorge Orduna Valls | |||||||||||||
Full Title: Prospective, randomized cohort study to evaluate the efficacy of two techniques against chronic knee pain: echo-guided radiofrequency over sensitive nerves of the knee, compared to intraarticular i... | |||||||||||||
Medical condition: Chronic knee pain (more than 3 months), in patients either non eligible for knee surgery, or with pain after three months of knee surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004541-82 | Sponsor Protocol Number: SupClun_1-1 | Start Date*: 2016-12-19 | |||||||||||
Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital | |||||||||||||
Full Title: Regional anaesthesia of the cutaneous nerves of the hip - A novel ultrasound guided nerve block of the superior cluneal nerves | |||||||||||||
Medical condition: Postoperative pain after hip surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001027-33 | Sponsor Protocol Number: PAFIBAR1.0 | Start Date*: 2023-06-07 | |||||||||||
Sponsor Name:FIMABIS | |||||||||||||
Full Title: Evaluation of the effect of Opioid-Free Anesthesia on oxygenation in bariatric surgery | |||||||||||||
Medical condition: Bariatric surgery | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024538-51 | Sponsor Protocol Number: ssgt05 | Start Date*: 2012-03-02 |
Sponsor Name:Silvia Gil Trujillo | ||
Full Title: Study of the effects of pregabalin in postoperative pain control in general total intravenous anesthesia, general inhalation anesthesia and combined anesthesia after abdominal hysterectomy. | ||
Medical condition: The presence of acute postoperative pain remains a major cause of preoperative morbidity.The objective is to evaluate the analgesic efficacy of pregabalin in the postoperatory of abdominal hysterec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001011-36 | Sponsor Protocol Number: ICO-A-2016-04 | Start Date*: 2017-05-24 | |||||||||||
Sponsor Name:INSTITUT DE CANCEROLOGIE DE L'OUEST | |||||||||||||
Full Title: Multicentric, comparative, randomized, open study comparing an early post-operative prophylactic non-invasive ventilation (NIV) to standard post-operative care in patients at high-risk of respir... | |||||||||||||
Medical condition: Legally adult patient going to have an operation under loco-regional or general anesthesia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003116-37 | Sponsor Protocol Number: 2015-1 | Start Date*: 2015-10-22 |
Sponsor Name:Akershus University Hospital | ||
Full Title: Postoperative analgesia with oxycodone after caesarean section | ||
Medical condition: Women who have been operated for pregnancy with caesarean section | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002528-10 | Sponsor Protocol Number: SIVAA01 | Start Date*: 2017-07-06 |
Sponsor Name:Vestfold Hospital Trust | ||
Full Title: TOF trial: A randomized double blinded controlled Trial comparing low dose Of sugammadex and neostigmine aFter use of rocuronium during general anesthesia in patients undergoing non-cardiac surgery | ||
Medical condition: The study population will include all patients >18 years scheduled for an elective surgical procedure undergoing general anesthesia with intravenous drugs and non-depolarizing NMBA (rocuronium), wi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004770-16 | Sponsor Protocol Number: PNL_protocol_v01 | Start Date*: 2016-01-04 | |||||||||||
Sponsor Name:Jens Børglum | |||||||||||||
Full Title: Ultrasoundguided Transmuscular Quadratus Lumborum(TQL) block for percutaneous nephrolithotomy (PNL) - a randomized controlled trial | |||||||||||||
Medical condition: The postoperative pain after percutaneous nephrolithotomy(PNL) operation. Our one year retrospective study of patients treated with PNL, revealed that, 71% of all patients undergoing PNL operation... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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