- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Stellate.
Displaying page 1 of 1.
| EudraCT Number: 2013-005325-23 | Sponsor Protocol Number: SGB_HF_MEN | Start Date*: 2014-06-20 |
| Sponsor Name:Rijnstate Hospital | ||
| Full Title: Short-term Efficacy of Stellate Ganglion Block in Men to reduce Hot Flushes related to Androgen Deprivation Therapy | ||
| Medical condition: Hot flushes due to androgen deprivation therapy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001180-36 | Sponsor Protocol Number: 2015-2158 | Start Date*: 2016-12-01 |
| Sponsor Name:Rijnstate Hospital | ||
| Full Title: Short-term Efficacy of Stellate Ganglion Block to reduce Hot Flushes | ||
| Medical condition: Hot Flushes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001806-40 | Sponsor Protocol Number: STATLiver2019 | Start Date*: 2019-09-03 | |||||||||||
| Sponsor Name:Afsnit 360, Gastroenheden | |||||||||||||
| Full Title: Statins for prevention of disease progression and hospitalization in Liver Cirrhosis: A multi-center, randomized, double blind, placebo-controlled trial. The STATLiver Trial. | |||||||||||||
| Medical condition: Cirrhosis of the liver | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| 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: 2011-003523-35 | Sponsor Protocol Number: 2 | Start Date*: 2011-10-28 | |||||||||||
| Sponsor Name:Department of Anaesthesia | |||||||||||||
| Full Title: A comparison of interscalene brachial plexus block combined with stellate ganglion block versus interscalene brachial plexus block for postoperative analgesia in major orthopaedic surgery of the up... | |||||||||||||
| Medical condition: We propose that an interscalene brachial plexus block combined with stellate ganglion block will give superior postoperative analgesia compared to interscalene brachial plexus block alone in majo... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001856-51 | Sponsor Protocol Number: 12.007 | Start Date*: 2014-08-26 | |||||||||||
| Sponsor Name:Aleksander Krag | |||||||||||||
| Full Title: Anti-fibrotic and molecular aspects of rifaximin in alcoholic liver disease: A randomized placebo controlled clinical trial | |||||||||||||
| Medical condition: Liver fibrosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004419-24 | Sponsor Protocol Number: RHMMED0687 | Start Date*: 2007-03-16 | |||||||||||
| Sponsor Name:Southampton University Hospitals Trust (R&D) | |||||||||||||
| Full Title: The Use of Sulfasalazine as an Anti-fibrotic in Acute Alcoholic Hepatitis | |||||||||||||
| Medical condition: Acute Alcoholic Hepatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003516-31 | Sponsor Protocol Number: NEOPACHI-001 | Start Date*: 2012-11-29 |
| Sponsor Name:CUB Erasme Hospital | ||
| Full Title: Evaluation of tumoral perfusion modification by dynamic imaging after neoadjuvant chemotherapy combining gemcitabine and a Hedgehog inhibitor (Vismodegib) in patients with resectable pancreatic ade... | ||
| Medical condition: Potentially resectable pancreatic ductal adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006221-77 | Sponsor Protocol Number: CRO 768 | Start Date*: 2007-06-26 | |||||||||||||||||||||
| Sponsor Name:Clinical Research office, Faculty of Medicine, Imperial College London | |||||||||||||||||||||||
| Full Title: Warfarin Anticoagualtion for liver fibrosis in patients transplanted for hepatitis C virus infection. | |||||||||||||||||||||||
| Medical condition: Liver fibrosis in patients infected with hepatitis C virus after liver transplantation. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2012-003592-19 | Sponsor Protocol Number: NEOPAX-001 | Start Date*: 2012-12-11 |
| Sponsor Name:CUB Erasme Hospital | ||
| Full Title: Evaluation of tumoral perfusion modification by dynamic imaging after chemotherapy combining gemcitabine and nab-paclitaxel (Abraxane) in patients with potentially operable, locally advanced or met... | ||
| Medical condition: Resectable (cohort 1) and locally advanced or metastatic (cohort 2) pancreatic ductal adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001979-70 | Sponsor Protocol Number: IVA_01_337_HNAS_16_002 | Start Date*: 2017-01-23 | |||||||||||
| Sponsor Name:Inventiva S.A. | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, multicenter, dose-range, proof-of-concept, 24-week treatment study of IVA337 in adult subjects with nonalcoholic steatohepatitis (NASH) | |||||||||||||
| Medical condition: Nonalcoholic steatohepatitis (NASH) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) CZ (Completed) AT (Completed) PT (Completed) ES (Completed) NL (Completed) PL (Completed) FR (Completed) BG (Completed) SI (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002488-88 | Sponsor Protocol Number: GS-US-321-0105 | Start Date*: 2013-07-29 | |||||||||||
| Sponsor Name:Gilead Sciences Inc | |||||||||||||
| Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of GS-6624, a Monoclonal Antibody Against Lysyl Oxidase-Like 2 (LOXL2), in Subjects w... | |||||||||||||
| Medical condition: Advanced Liver Fibrosis Secondary to Non-Alcoholic Steatohepatitis (NASH) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) DE (Prematurely Ended) GB (Prematurely Ended) ES (Completed) BE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002489-11 | Sponsor Protocol Number: GS-US-321-0106 | Start Date*: 2013-02-26 | |||||||||||
| Sponsor Name:Gilead Sciences Inc | |||||||||||||
| Full Title: A Phase 2b, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled Trial Evaluating the Safety and Efficacy of GS-6624, a Monoclonal Antibody Against Lysyl Oxidase-Like 2 (LOXL2), in Subjects w... | |||||||||||||
| Medical condition: Compensated Cirrhosis Secondary to Non-Alcoholic Steatohepatitis (NASH) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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