- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
22 result(s) found for: Sympathetic nervous system.
Displaying page 1 of 2.
EudraCT Number: 2009-010557-12 | Sponsor Protocol Number: Version1.0/Jan2009 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:The Pennine Acute Hospitals NHS Trust | |||||||||||||
Full Title: A Single Blind, Randomised, Cross-over Study to Compare the Efficacy of Lidocaine 5% Plasters(Versatis) versus Pregabalin (Lyrica) in the Treatment of Complex Regional Pain Syndrome, Type 1. | |||||||||||||
Medical condition: Complex regional pain syndrome type 1. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001164-11 | Sponsor Protocol Number: KF7013-03 | Start Date*: 2017-04-24 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Open-label safety trial of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS) | ||||||||||||||||||
Medical condition: Complex regional pain syndrome (CRPS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001915-37 | Sponsor Protocol Number: KF7013-01 | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, double-blind trial investigating the efficacy and safety of intravenous neridronic acid in subjects with complex regional pain syndrome type I (CRPS-I) | |||||||||||||
Medical condition: Complex regional pain syndrome type I (CRPS-I) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004750-21 | Sponsor Protocol Number: TAK-935-2008 | Start Date*: 2019-06-10 | ||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, a wholly owned subsidiary of Takeda | ||||||||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-935 as an Adjunctive Therapy in Adult Subjects With Chronic Complex Regional... | ||||||||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003833-91 | Sponsor Protocol Number: KF7013-02 | Start Date*: 2018-10-04 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial investigating the efficacy and safety of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS) | ||||||||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005557-24 | Sponsor Protocol Number: 69HCL18_0996 | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique et de l'Innovation | |||||||||||||
Full Title: Étude pilote visant à évaluer l’efficacité d’un mélange de kétamine/lidocaïne administré par mésothérapie dans la prise en charge des douleurs neuropathiques du Syndrome Douloureux Régional Complex... | |||||||||||||
Medical condition: Complex regional pain syndrome type I | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004460-66 | Sponsor Protocol Number: KARAASS-1 | Start Date*: 2014-04-01 | ||||||||||||||||
Sponsor Name:Jørgen Jeppesen | ||||||||||||||||||
Full Title: Oral potassium supplementation in healthy men - interactions with the renin-angiotensin-aldosterone system and the sympathetic nervous system | ||||||||||||||||||
Medical condition: Blood pressure regulation and hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002202-43 | Sponsor Protocol Number: Empa_MIBG | Start Date*: 2021-04-28 | |||||||||||
Sponsor Name:AOU FEDERICO II | |||||||||||||
Full Title: Effects of empagliflozin on cardiac remodeling and myocardial sympathetic nervous system in diabetic patients affected by chronic heart failure | |||||||||||||
Medical condition: diabetes mellitus and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002767-41 | Sponsor Protocol Number: mobil-c1 | Start Date*: 2008-02-29 |
Sponsor Name:Sonderforschungsbereich 656 (SFB 656) | ||
Full Title: Kardiale Innervation bei genetischen Arrhythmiemodellen in Menschund Maus | ||
Medical condition: The longQT-syndrome is a genetically detemined malfunction of ion channels. The identified genes in longQT-patients encode cardiac ion channels or accessory proteins affecting the function of diffe... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004878-17 | Sponsor Protocol Number: 0.1 | Start Date*: 2017-07-20 |
Sponsor Name:University of Leicester | ||
Full Title: The Effect of a SGLT2 inhibitor on Glucose flux, Lipolysis and Exercise in type 2 Diabetes | ||
Medical condition: Type 2 diabetes. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2009-010708-28 | Sponsor Protocol Number: none02 | Start Date*: 2009-07-03 | |||||||||||
Sponsor Name:Department of Anaesthesia | |||||||||||||
Full Title: Does the stellate ganglion block improve postoperative analgesia following upper limb trauma? | |||||||||||||
Medical condition: We propose that the sympathetic nervous system contributes to acute pain and that a sympathetic nerve block, the stellate ganglion block, will improve postoperative pain in patients presenting for ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015867-15 | Sponsor Protocol Number: DBS | Start Date*: 2010-02-18 |
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | ||
Full Title: Different Anesthesiological Strategies Evaluation in Deep Brain Stimulation Neurosurgeries | ||
Medical condition: Parkinson Desease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004664-23 | Sponsor Protocol Number: ST 200 DS 05-01 | Start Date*: 2006-05-25 | |||||||||||
Sponsor Name:SIGMA-TAU | |||||||||||||
Full Title: The role of Acetyl-L-Carnitine in Reflex Sympathetic Dystrophy RDS and in Complex Regional Pain Syndrome CRPS .Pilot clinical trial. | |||||||||||||
Medical condition: Reflex Sympathetic Dystrophy RDS and Complex Regional Pain Syndrome CRPS . | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002256-16 | Sponsor Protocol Number: 19-01SPIOMI | Start Date*: 2020-01-28 | |||||||||||
Sponsor Name:Fraunhofer Society | |||||||||||||
Full Title: Acute and two-week effects of Spiolto® Respimat® (Tiotropium/Olodaterol) on cardiac function, the autonomic nervous system and small airway function in hyperinflated COPD subjects | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022579-68 | Sponsor Protocol Number: COR-1/02 | Start Date*: 2011-08-16 | |||||||||||
Sponsor Name:Corimmun GmbH | |||||||||||||
Full Title: COR-1, an anti-ß1 receptor antibody cyclopeptide in heart failure: a phase II, multicentre, randomised, double-blind and placebo-controlled study with parallel groups | |||||||||||||
Medical condition: Heart Failure, Dilated Cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001840-37 | Sponsor Protocol Number: 2017-001840-37 | Start Date*: 2019-01-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: ERtugliflozin triAl in DIabetes with preserved or reduced ejeCtion FrAcTion mEchanistic evaluation in Heart Failure: "ERADICATE-HF" | ||
Medical condition: Diabetes Mellitus Type 2 and Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003005-61 | Sponsor Protocol Number: BGP-15-CLIN-06 | Start Date*: 2020-09-30 | |||||||||||
Sponsor Name:Sinusventure LLC. | |||||||||||||
Full Title: A phase 2 study on the clinical efficacy of adjuvant BGP-15 treatment additional to beta-blocker bisoprolol in patients with inappropriate sinus tachycardia | |||||||||||||
Medical condition: Inappropriate sinus tachycardia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001581-18 | Sponsor Protocol Number: SCO114520 | Start Date*: 2012-03-29 | |||||||||||
Sponsor Name:GlaxoSmithKline GmbH & Co. KG | |||||||||||||
Full Title: Effects of bronchodilatation with salmeterol on the autonomic nervous system | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001542-17 | Sponsor Protocol Number: T109/2019Xe-SAH | Start Date*: 2020-09-17 | |||||||||||
Sponsor Name:Timo Laitio | |||||||||||||
Full Title: Effect of xenon on brain injury, neurological outcome and survival in patients after aneurysmal subarachnoid hemorrhage | |||||||||||||
Medical condition: Acute rupture of cerebral aneurysm, subarachnoid hemorrhage (SAH), unconsciousness, brain injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006609-25 | Sponsor Protocol Number: MOOD-HF | Start Date*: 2008-05-27 | |||||||||||
Sponsor Name:Julius Maximilians Universität Würzburg | |||||||||||||
Full Title: Effects of selective serotonin re-uptake inhibition on morbidity, mortality and mood in Depressed Heart Failure patients | |||||||||||||
Medical condition: To investigate the effects of selective serotonin re-uptake inhibition with the SSRI escitalopram on morbidity and mortality in depressed patients with CHF. The primary endpoint is the time to a fi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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