- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
26 result(s) found for: Decompression.
Displaying page 1 of 2.
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: 2021-004756-42 | Sponsor Protocol Number: DIA2021-08 | Start Date*: 2022-01-25 | |||||||||||||||||||||
Sponsor Name:Diakonhjemmet sykehus | |||||||||||||||||||||||
Full Title: The NOR-CACTUS Trial: A NORwegian trial CompAring treatment strategies for Carpal TUnnel Syndrome | |||||||||||||||||||||||
Medical condition: Carpal tunnel syndrome - median neuropathy caused by nerve entrapment at the site of the carpal tunnel in the wrist | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001286-42 | Sponsor Protocol Number: ABI 55-0603-1 | Start Date*: 2006-09-20 |
Sponsor Name:Aastrom Biosciences, Inc | ||
Full Title: Multi-center, Multi-national Clinical Trial of the Application of Tissue Repair Cell (TRC) Therapy of Osteonecrosis in the Femur Head | ||
Medical condition: Osteonecrosis of the femur head | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000624-20 | Sponsor Protocol Number: ILONA | Start Date*: 2021-06-17 | |||||||||||
Sponsor Name:Leipzig University | |||||||||||||
Full Title: Core decompression versus core decompression followed by infusion of Iloprost in the treatment of non-traumatic avascular necrosis of the femoral head | |||||||||||||
Medical condition: non-traumatic avascular necrosis of the femoral head (N-ANFH) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003513-32 | Sponsor Protocol Number: KMS/TW/2005032 | Start Date*: 2005-08-31 |
Sponsor Name:South Tees Hospitals NHS Trust | ||
Full Title: A Randomised controlled trial to compare the efficacy of two types of local anaesthetic blocks in carpal tunnel decompression surgery | ||
Medical condition: Carpal Tunnel Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003082-15 | Sponsor Protocol Number: KTB-002 | Start Date*: 2011-09-08 | ||||||||||||||||
Sponsor Name:Karen Toftdahl Bjørnholdt | ||||||||||||||||||
Full Title: High dose dexamethasone for pain following arthroscopic shoulder surgery: A randomised blinded clinical trial. | ||||||||||||||||||
Medical condition: Pain following arthroscopic shoulder surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002801-23 | Sponsor Protocol Number: Metamizole002 | Start Date*: 2019-10-08 |
Sponsor Name:Jessa Hospital | ||
Full Title: Evaluation of the added value of Metamizole to standard post-operative treatment after ambulant surgery: a double-blind, randomized controlled trial | ||
Medical condition: Optimalization of post-operative treatment after ambulant surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001055-40 | Sponsor Protocol Number: 111-209 | Start Date*: 2020-07-29 | |||||||||||
Sponsor Name:BioMarin Pharmaceutical Inc. | |||||||||||||
Full Title: A randomized, controlled, open-label clinical trial with an open-label extension to investigate the safety of BMN 111 in infants and young children with achondroplasia at risk of requiring cervicom... | |||||||||||||
Medical condition: achondroplasia | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004237-21 | Sponsor Protocol Number: Metamizole003 | Start Date*: 2020-11-27 |
Sponsor Name:Jessa Hospital | ||
Full Title: Evaluation of the added value of Metamizole to standard postoperative treatment after ambulant shoulder surgery: a double-blind, randomized controlled trial | ||
Medical condition: Optimalisation of postoperative treatment after ambulant shoulder arthroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002917-12 | Sponsor Protocol Number: PTHspinalstenos4 | Start Date*: 2011-12-06 |
Sponsor Name:Department of Orthopaedics IKE [...] | ||
Full Title: Does PTH enhance healing after spinal fusion? | ||
Medical condition: Decompression and fusion due to spinal stenosis in men and postmenopausal women. In this study we want to examine if Forsteo (teriparatide) improves bone healing (jugded by blinded investigators) a... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003590-25 | Sponsor Protocol Number: NL | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: a Randomized controlled trial for epidural Analgesia for Pain relief after lumbar Interlaminar Decompressive spine surgery - RAPID | |||||||||||||
Medical condition: Lumbar spinal stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002096-29 | Sponsor Protocol Number: iVRCT | Start Date*: 2015-07-20 | ||||||||||||||||
Sponsor Name:Speising Orthopaedic Hospital Vienna | ||||||||||||||||||
Full Title: Application of Intrawound Vancomycin Powder in Spinal Fusion Surgery to Reduce Postoperative Surgical Site Infections - A Prospective Randomized Controlled Trial | ||||||||||||||||||
Medical condition: Postoperative surgical site infections (deep and superficial) after spinal fusion surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003637-14 | Sponsor Protocol Number: AGO/2018/004 | Start Date*: 2019-03-29 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Local injection of collagenase clostridium histolyticum (XiapexR) for refractory gastrointestinal strictures: an open-label pilot study. | |||||||||||||
Medical condition: refractory iatrogenic gastrointestinal strictures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023426-20 | Sponsor Protocol Number: AUGUST-2 | Start Date*: 2011-04-08 |
Sponsor Name:GWT-TUD GmbH | ||
Full Title: Low dose Urokinase therapy in patients with diabetic foot syndrome, critical limb ischemia as well as rest ischemia or missing of option revascularisation in comparison to the standard therapy - ra... | ||
Medical condition: Diabetic foot syndrome with critical limb ischemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-002815-32 | Sponsor Protocol Number: DXMPN2017 | Start Date*: 2017-10-05 |
Sponsor Name:AZ Groeninge | ||
Full Title: The dose response of Dexamethasone as perineural adjuvant in Brachial Plexus Block. | ||
Medical condition: postoperative pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000093-25 | Sponsor Protocol Number: 01_20012022 | Start Date*: 2022-05-05 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: The effect of lateral pectoral nerve block in combination with interscalene nerve block on opioid consumption and pain on awake shoulder arthroscopy patients - A feasibility study | |||||||||||||
Medical condition: Peri- and postoperative pain after shoulder arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004856-41 | Sponsor Protocol Number: CCTU0178 | Start Date*: 2020-03-19 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | ||
Full Title: Regeneration in Cervical Degenerative Myelopathy - a multi-centre, double-blind, randomised, placebo controlled trial assessing the efficacy of Ibudilast as an adjuvant treatment to decompressive s... | ||
Medical condition: Degenerative Cervical Myelopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003669-17 | Sponsor Protocol Number: NEOPA | Start Date*: 2013-12-17 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Sequential neoadjuvant chemoradiotherapy (CRT) followed by curative surgery vs. primary surgery alone for resectable, non-metastasized pancreatic adenocarcinoma (NEOPA). | |||||||||||||
Medical condition: Non-metastasized, adenocarcinoma of the pancreatic head/uncinate process or body of pancreas that was treated with extended pancreatic head/body resection larger than 2 cm in size (≥cT2) and/or in ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012672-27 | Sponsor Protocol Number: CIP0702PLF/EU | Start Date*: 2009-08-17 | |||||||||||
Sponsor Name:ApaTech Limited | |||||||||||||
Full Title: "A prospective, randomised study comparing the use of Actifuse™ ABX synthetic bone substitute with INFUSE® in patients requiring posterolateral instrumented lumbar fusion with interbody fusion" als... | |||||||||||||
Medical condition: Prospective trial participants will have been diagnosed with degenerative disc disease with a treatment option of decompression and Interbody Fusion with Posterolateral Intertransverse Process Fusi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004258-24 | Sponsor Protocol Number: FBA | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:UNIVERSITA' CAMPUS BIOMEDICO | |||||||||||||
Full Title: Clinical trial to study application of MESNA for infiltration into the epidural ''Failed Back Syndrome'' (FBS) | |||||||||||||
Medical condition: Failed Back Syndrome | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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