- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
24 result(s) found for: Ulnar nerve.
Displaying page 1 of 2.
EudraCT Number: 2022-003201-30 | Sponsor Protocol Number: 1.0-03.10.2022 | Start Date*: 2022-12-22 |
Sponsor Name:Medical University Vienna | ||
Full Title: The Impact of Biological Gender in Peripheral Nerve Blockade: A Prospective Study in Volunteers | ||
Medical condition: To evaluate pharmacodynamic, pharmacokinetic and nerve-related morphometric differences of biological gender (male versus female) on nerve block characteristics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-002608-34 | Sponsor Protocol Number: ArAL11.1 | Start Date*: 2011-11-21 | |||||||||||
Sponsor Name:Paula Diéguez García | |||||||||||||
Full Title: Comparation of the efficacy and onset of the distribution circumferencial va not ircumferencial of local anesthetic in the median and ulnar nerves for surgery of carpal tunnel | |||||||||||||
Medical condition: Sheduled patients for surgery of carpal tunnel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002835-14 | Sponsor Protocol Number: SCCCSH01 | Start Date*: 2016-10-07 | |||||||||||
Sponsor Name:Nordsjællands Hospital Hillerød | |||||||||||||
Full Title: Supraclavicular catheter for regional anesthesia of the shoulder - an explorative study in healthy volunteers. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001221-98 | Sponsor Protocol Number: 1.3 | Start Date*: 2018-06-25 |
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | ||
Full Title: DEXAMETHASONE AS ADJUVANT FOR PERIPHERAL NERVE BLOCKADE: A RANDOMIZED, TRIPLE-BLINDED AND CROSSOVER STUDY IN VOLUNTEERS | ||
Medical condition: The combination of local anaesthetics plus dexamethasone shall increase the duration of regional anaesthetic blocks. It is a volunteers´study. Three different block combination are performed. One b... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003790-10 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-10-23 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Klinische Pharmakologie | ||
Full Title: DEXMEDETOMIDINE FOR PERIPHERAL NERVE BLOCKADE: A DOSE-FINDING STUDY IN VOLUNTEERS | ||
Medical condition: 24 Volunteers recieve an ultrasound guided ulnar nerve block, and apparted into 4 groups. Group 1 receives 3ml Ropivacaine 0.75% without adjuvants. Group 2-4 receives 3ml Ropivacain 0.75% with thre... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-002810-15 | Sponsor Protocol Number: CHUB-Neuro-ENMG-MS | Start Date*: 2021-06-25 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Peripheral neuropathy as potential side effect in patients with multiple sclerosis treated with teriflunomide. | |||||||||||||
Medical condition: Multiple sclerosis, treated with teriflunomide | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000035-74 | Sponsor Protocol Number: 1.1_27.02.2023 | Start Date*: 2023-03-05 |
Sponsor Name:Medical University Vienna | ||
Full Title: Pharmacodynamics of Liposomal Bupivacaine for Peripheral Nerve Blockade: A Randomized, Triple-blinded, Cross Over Study in Volunteers | ||
Medical condition: To evaluate the pharmacodynamic effects of perineural administered liposomal bupivacaine on nerve block characteristics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2016-004883-20 | Sponsor Protocol Number: SM1-JH-16 | Start Date*: 2017-02-01 | |||||||||||
Sponsor Name:Ole Mathiesen | |||||||||||||
Full Title: Does perineural dexmedetomidine prolong the duration of an ulnar nerve block when controlling for possible systemic effects? - a randomized, blinded, placebo controlled, paired trial in healthy vo... | |||||||||||||
Medical condition: Healthy volunteers (treatment intended to improve regional anesthesia for orthopedic surgery) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004921-33 | Sponsor Protocol Number: R475-OA-1758 | Start Date*: 2018-11-09 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Effects of Fasinumab on Peripheral Nerve Function in Patients with Pain Due to Osteoarthritis of the Hip or Knee | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002378-19 | Sponsor Protocol Number: CLN-PXT3003-02 | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:PHARNEXT | |||||||||||||
Full Title: International, multi-center, randomized, double-blind, placebo-controlled phase III study assessing in parallel groups the efficacy and safety of 2 doses of PXT3003 in patients with Charcot-Marie-T... | |||||||||||||
Medical condition: Charcot-Marie-Tooth Disease - Type 1A | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Suspended by CA) ES (Completed) BE (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011829-13 | Sponsor Protocol Number: AN09/8905 | Start Date*: 2009-11-02 |
Sponsor Name:University of Leeds | ||
Full Title: What is the ED95 dose for bupivacaine for supraclavicular brachial plexus block using ultrasound? | ||
Medical condition: Patients presenting for routine upper limb surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-006493-23 | Sponsor Protocol Number: NIMAO/2021-1/YG-01 | Start Date*: 2022-04-04 | ||||||||||||||||||||||||||
Sponsor Name:Nimes University Hospital | ||||||||||||||||||||||||||||
Full Title: Evaluation of the patient postoperative experience of two modes of WALANT-type anesthesia (lidocaine alone or combined with ropivacaine) used in ambulatory upper-extremity surgery | ||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001656-22 | Sponsor Protocol Number: 1601 | Start Date*: 2016-11-17 | |||||||||||
Sponsor Name:Ziekenhuis Oost Limburg | |||||||||||||
Full Title: The utility of liposomal bupivacaine for anesthesia and analgesia in patients treated with collagenase for the release of Dupuytren’s contracture: A randomized controlled trial. | |||||||||||||
Medical condition: Introduction of collagenase clostridium histolyticum injection for the treatment of Dupuytren’s contractures. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004670-10 | Sponsor Protocol Number: AG10-333 | Start Date*: 2020-07-07 | |||||||||||
Sponsor Name:Eidos Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of AG10 in Subjects with Symptomatic Transthyretin Amyloid Polyneuropathy (ATTRibute-PN Trial) | |||||||||||||
Medical condition: Symptomatic Transthyretin Amyloid Polineuropathy (ATTR-PN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) DE (Prematurely Ended) PT (Prematurely Ended) FR (Completed) BG (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000585-30 | Sponsor Protocol Number: I16016 | Start Date*: 2017-12-13 | ||||||||||||||||
Sponsor Name:CHU de Limoges | ||||||||||||||||||
Full Title: Pilot study, single-blind, candesartan versus usual care of peripheral neuropathy development induced by vincristine (PNIV) in patients treated for lymphoma B. | ||||||||||||||||||
Medical condition: peripheral neuropathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002053-19 | Sponsor Protocol Number: CLMI070X2201 | Start Date*: 2014-12-16 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An open-label multi-part first-in-human study of oral LMI070 in infants with Type 1 spinal muscular atrophy | |||||||||||||
Medical condition: Spinal Muscular Atrophy | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) IT (Completed) DE (Completed) BE (Completed) NL (Ongoing) CZ (Completed) PL (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005557-73 | Sponsor Protocol Number: I10E-1302 | Start Date*: 2014-10-21 | |||||||||||
Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
Full Title: An international, multicentre, efficacy and safety study of I10E in initial and maintenance treatment of patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000004-13 | Sponsor Protocol Number: ST200-DM-04-005 | Start Date*: 2005-09-16 | |||||||||||
Sponsor Name:Sigma-Tau i.f.r. S.p.A. | |||||||||||||
Full Title: EVALUATION OF ACETYL -L-CARNITINE (ST 200) TO REDUCE INTENSITY OF TAXANES- OR PLATINUM-INDUCED SENSORY NEUROPATHY | |||||||||||||
Medical condition: Peripheral neurophaty in cancer patients previously treated with taxanes- or platinum-based chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005558-31 | Sponsor Protocol Number: I10E-1306 | Start Date*: 2015-01-08 | |||||||||||
Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
Full Title: International, multicentre, efficacy and safety study of I10E in the maintenance treatment of patients with Chronic Inflammatory Demyelinating Polyradiculoneuropathy: Extension of PRISM study I1... | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Completed) IT (Prematurely Ended) FR (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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