- Trials with a EudraCT protocol (146)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
146 result(s) found for: Sensory nerve.
Displaying page 1 of 8.
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: 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: 2014-000299-25 | Sponsor Protocol Number: 1.4 | Start Date*: 2014-12-05 |
Sponsor Name:Unfallkrankenhaus Salzburg | ||
Full Title: Dexmedetomidine for saphenous nerve blockade in patients undergoing anterior cruciate ligament replacement: a randomized, placebo-controlled, triple blinded study | ||
Medical condition: Dexmedetomidine -a selective alpha-2-receptor agonist- added to a local anaesthetic (ropivacaine) should prolong a saphenous block and the patients demand for the first analgesic. We designed a pro... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
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: 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: 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: 2011-004033-13 | Sponsor Protocol Number: EMA401-005 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Spinifex Pharmaceuticals Pty Ltd | |||||||||||||
Full Title: A Phase 2 open label biomarker study of angiotensin II type 2 receptor antagonist EMA401 for the treatment of pain in patients with chemotherapy-induced peripheral neuropathy. | |||||||||||||
Medical condition: Chemotherapy induced peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016038-29 | Sponsor Protocol Number: LIDO-2009 | Start Date*: 2010-03-11 | ||||||||||||||||
Sponsor Name:Danish Pain Research Center | ||||||||||||||||||
Full Title: Topical lidocaine: Predictors of response in peripheral nerve damage | ||||||||||||||||||
Medical condition: Neuropathic pain due to Peripheral nerve damage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003213-98 | Sponsor Protocol Number: LFCN_1-1_20160802 | Start Date*: 2016-10-14 | |||||||||||
Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital | |||||||||||||
Full Title: The lateral femoral cutaneous nerve – description of the sensory territory and a novel ultrasound guided nerve block technique | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002570-30 | Sponsor Protocol Number: EFC5505 | Start Date*: 2005-12-07 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Recherche | |||||||||||||
Full Title: A multicenter, randomized double-blind placebo controlled Phase III study of the efficacy of xaliproden in preventing the neurotoxicity of oxaliplatin in first-line treatment of patients with metas... | |||||||||||||
Medical condition: Patients with metastatic colorectal cancer treated with oxaliplatin/5-FU/LV; at risk of cumulative peripheral sensory neuropathy (PSN) relative to cumulative dose of oxaliplatin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) ES (Completed) PT (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000348-14 | Sponsor Protocol Number: NSTATIN | Start Date*: 2014-03-05 |
Sponsor Name:Odense University Hospital, Department of Neurology | ||
Full Title: Statin-treatment and peripheral neuropathy - a randomized clinical trial | ||
Medical condition: Patients with cerebral infarction or transient ischemic attack. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-013462-25 | Sponsor Protocol Number: MW001 | Start Date*: 2009-09-28 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde Health Board | |||||||||||||
Full Title: A dose finding study for ultrasound guided anterior psoas compartment blocks in patients with a fractured neck of femur | |||||||||||||
Medical condition: Proximal traumatic fractured neck of femur | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 2009-013481-10 | Sponsor Protocol Number: 437 | Start Date*: 2009-10-14 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Pharmacokinetics of high dose Ropivacaine with and without epinephrine for combined femoral and sciatic nerve block in lower extremity surgery. A pilot study. | ||
Medical condition: combined femoral and sciatic nerve block for lower extremity orthopedic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003684-54 | Sponsor Protocol Number: ACLS | Start Date*: 2014-03-27 |
Sponsor Name:Academic Medical Center Amsterdam | ||
Full Title: Analgesic efficacy of saphenous nerve blockade for outpatient knee anterior cruciate ligament surgery | ||
Medical condition: Mid thigh saphenous nerve block with levobupivacain, as compared to femoral nerve block, in patients undergoing anterior cruciate ligament surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000902-82 | Sponsor Protocol Number: D8000-003 | Start Date*: 2022-05-24 | |||||||||||
Sponsor Name:Alzecure Pharma AB | |||||||||||||
Full Title: A Phase 2a, randomised, double-blind, placebo-controlled crossover study to explore the effects of ACD440 in patients with peripheral neuropathic pain with sensory hypersensitivity | |||||||||||||
Medical condition: Peripheral neuropathic pain with sensory hypersensitivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001246-17 | Sponsor Protocol Number: CBX129801-DN-201 | Start Date*: 2013-05-28 |
Sponsor Name:Cebix Incorporated | ||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of CBX129801 (Ersatta™), Long-Acting Synthetic C-Peptide, in Type 1 Diabetes Mellitus Subjects wit... | ||
Medical condition: Mild to moderate diabetic peripheral neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003694-34 | Sponsor Protocol Number: 2-HIT | Start Date*: 2017-10-25 | ||||||||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | ||||||||||||||||||
Full Title: Onset and duration of Forearm nerve blockade performed with a single distal injection versus sequential injections at distal and proximal locations alongside the nerves: a blinded randomized contro... | ||||||||||||||||||
Medical condition: Dupuytren contrature and Carpal Tunnel syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006235-33 | Sponsor Protocol Number: 738/02/2011 | Start Date*: 2012-03-30 | |||||||||||
Sponsor Name:MDM S.P.A. | |||||||||||||
Full Title: Sensory Motor Neuropathies of the sciatic nerve: a comparative evaluation of dextrorotatory enantiomer of thioctic acid and acetyl-L-carnitine. | |||||||||||||
Medical condition: sensitive motor sciatic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003695-31 | Sponsor Protocol Number: FIB | Start Date*: 2017-12-04 | |||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | |||||||||||||
Full Title: Fascia iliaca block for analgesia in unilateral direct anterior approach total hip arthroplasty | |||||||||||||
Medical condition: Total hip arthroplasty through minimal invasive muscle sparing surgery technique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
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