- Trials with a EudraCT protocol (318)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
318 result(s) found for: Local anesthesia.
Displaying page 1 of 16.
EudraCT Number: 2021-001854-74 | Sponsor Protocol Number: RBHP-2021-ELJEZI | Start Date*: 2021-07-28 | ||||||||||||||||
Sponsor Name:CHU de Clermont-Ferrand | ||||||||||||||||||
Full Title: - | ||||||||||||||||||
Medical condition: - | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005555-15 | Sponsor Protocol Number: | Start Date*: 2007-08-17 | |||||||||||
Sponsor Name:Univ.-Prof. Dr. Doris Balogh | |||||||||||||
Full Title: increased efficacy of lidocaine when amitriptyline is added for local anaesthesia | |||||||||||||
Medical condition: The objective of the present study is to investigate whether a combination of ultra-low-dose amitriptyline with the conventional local anesthetic lidocaine enhances the anesthetic effect of the lat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
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: 2015-003498-13 | 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: 2007-000702-71 | Sponsor Protocol Number: PreSpiDi2006-01 | Start Date*: 2007-07-13 | ||||||||||||||||
Sponsor Name:Alysis Zorggroep | ||||||||||||||||||
Full Title: The effect of intravenous fluid preload on diuresis during spinal anesthesia-induced detrusor blockade | ||||||||||||||||||
Medical condition: Diuresis during spinal anesthesia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003972-37 | Sponsor Protocol Number: CLVSPR19 | Start Date*: 2020-06-05 |
Sponsor Name:Hospital Arnau de Vilanova - Lliria | ||
Full Title: Comparative study of cloroprocaine versus prilocaine intrathecal anestesia in major ambulatory surgery | ||
Medical condition: Inguinal hernia liable to ambulatory surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001413-24 | Sponsor Protocol Number: 35RC15_8933_TAP-ALIF | Start Date*: 2016-06-22 | |||||||||||
Sponsor Name:CHU de Rennes | |||||||||||||
Full Title: Intérêt du TAP (Transverse Abdominis Plane) bloc bilatéral échoguidé pour l’analgésie post opératoire des chirurgies rachidiennes par voie antérieure. | |||||||||||||
Medical condition: Chirurgie du rachis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000882-29 | Sponsor Protocol Number: 001 | Start Date*: 2016-02-18 | |||||||||||
Sponsor Name:Reinier de Graaf Groep | |||||||||||||
Full Title: Spinal hyperbaric Prilocaine 2% 60 or 80 mg: a dosing study in day care patients. | |||||||||||||
Medical condition: spinal anesthesia for open inguinal hernia repair or lower limb surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000166-21 | Sponsor Protocol Number: 1 | Start Date*: 2007-06-22 | |||||||||||
Sponsor Name:Whipps Cross University Hospital | |||||||||||||
Full Title: A comparison of the efficacy of 10% lidocaine solution and EMLA cream as local anaesthetic for the insertion of tympanic membrane ventilation tubes. | |||||||||||||
Medical condition: Grommet/ventilation tube insertion in adults with otitis media with effusion (glue ear). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000254-13 | Sponsor Protocol Number: RD/613/07 | Start Date*: 2008-10-14 | ||||||||||||||||
Sponsor Name:Gwent Healthcare NHS Trust | ||||||||||||||||||
Full Title: A double blind randomised placebo controlled study assessing the effect of intra-operative local anaesthetic administration on postoperative pain in adolescent children undergoing oral surgery unde... | ||||||||||||||||||
Medical condition: Postoperative pain following oral surgery in 12 to 16 year olds | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2021-000559-38 | Sponsor Protocol Number: BTXA2021 | Start Date*: 2022-07-02 | ||||||||||||||||
Sponsor Name:Herlev and Gentofte University Hospital, Department of Obstetrics and Gynecology | ||||||||||||||||||
Full Title: The effect of intravesical Lidocaine solution versus placebo as anesthesia prior to intravesical injection of onabotulinum toxin A. A randomized, double-blind, placebo controlled cross-over study | ||||||||||||||||||
Medical condition: The effect of intravesical Lidocaine solution versus placebo on pain perception during intravesical injection of Onabotulinum toxin A. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005177-27 | Sponsor Protocol Number: 2020-005177-27 | Start Date*: 2021-09-22 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Preoperative Viscous Lidocaine for Upper Gastrointestinal Endoscopy | |||||||||||||
Medical condition: Topical local anesthesia for upper gastrointestinal endoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
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: 2022-000559-35 | Sponsor Protocol Number: 0 | Start Date*: 2022-07-14 |
Sponsor Name:None | ||
Full Title: COMPLICATIONS AND DEGREE OF TOLERANCE OF THE ADMINISTRATION OF LOCAL ANESTHESIA IN DIAGNOSTIC / THERAPEUTIC THORACOCENTESIS PROCEDURES | ||
Medical condition: There is no consensus about the most appropriate local anesthetic, and 1% mepicavain and 2% lidocaine uses can be postulated indistinctly. This project was born with the intention of highlighting t... | ||
Disease: | ||
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: 2022-000857-10 | Sponsor Protocol Number: NA | Start Date*: 2022-05-16 |
Sponsor Name:CHU de Liège | ||
Full Title: Isobaric versus hyperbaric intrathecal bupivacaine: influence of baricity on blood pression variation during elective total knee arthroplasty: a randomized clinical trial. | ||
Medical condition: Total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000089-12 | Sponsor Protocol Number: HIP/FUSION#4 | Start Date*: 2018-04-24 | |||||||||||
Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
Full Title: Effect and safety of the iliopsoas plane block in healthy volunteers | |||||||||||||
Medical condition: No specific medical condition is investigated. The objective of the trial is to investigate a method for postoperative analgesia after elective hip surgery. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003675-11 | Sponsor Protocol Number: AT06/2011 | Start Date*: 2011-09-21 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Comparison of 2-chloroprocaïne, bupivacaïne and lidocaïne for spinal anesthesia in knee artroscopy in an outpatient setting: a double blind randomised trial | ||
Medical condition: spinal anesthesia in knee arthroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004504-29 | Sponsor Protocol Number: 49024 | Start Date*: 2015-02-25 |
Sponsor Name:Helse Fonna, Haugesund Sykehus | ||
Full Title: "Haemodynamic stability of bupivacaine with and without adrenaline for paracervical block during general anesthesia. A randomized controlled double blinded study." | ||
Medical condition: Cervical conisation is done for pre-cancer disease. The procedure is done with local anesthesia and general anesthesia. Local anesthesia is given by paracervical block, and several different local ... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
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