- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Lumbar nerve.
Displaying page 1 of 2.
EudraCT Number: 2010-023262-46 | Sponsor Protocol Number: 20101005PH | Start Date*: 2011-03-08 |
Sponsor Name:Royal Devon & exeter Foundation trust | ||
Full Title: A Randomised Prospective Pilot Study Comparing the Outcomes of Patients with Lumbar Nerve Root Pain Secondary to Lumbar Disc Prolapse Treated by Nerve Root Block with or without the Addition of Clo... | ||
Medical condition: Lumbar nerve root pain secondary to disc prolapse. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005346-10 | Sponsor Protocol Number: AUH-TFB-SR | Start Date*: 2014-11-21 | ||||||||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | ||||||||||||||||||
Full Title: Shamrock versus Lumbar Ultrasound Trident – Ultrasound guided block of the lumbar plexus | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006503-15 | Sponsor Protocol Number: STA-LDH01 | Start Date*: 2023-02-23 | |||||||||||||||||||||
Sponsor Name:Stayble Therapeutics | |||||||||||||||||||||||
Full Title: A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation | |||||||||||||||||||||||
Medical condition: Radiculopathy due to lumbar intervertebral disc herniation | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001678-26 | Sponsor Protocol Number: LOCAL/2018/PC-02 | Start Date*: 2019-09-11 | |||||||||||
Sponsor Name:CHU de NIMES | |||||||||||||
Full Title: Erectus nerve block for lumbar spine surgery : a prospective randomized study | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001449-26 | Sponsor Protocol Number: 6603/1132 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Seikagaku Corporation | |||||||||||||
Full Title: A Multicenter, Open-label Study of SI-6603 in Patients with Lumbar Disc Herniation (Phase III) | |||||||||||||
Medical condition: Lumbar disc herniation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003322-28 | Sponsor Protocol Number: BUP4006 | Start Date*: 2007-06-21 |
Sponsor Name:Norpharma A/S | ||
Full Title: A randomised, double-blind, multicentre non-inferiority study with active, parallel comparator group, to evaluate the efficacy and safety of Norspan® versus Tramadol in subjects with chronic, mode... | ||
Medical condition: Chronic, moderate to severe osteoarthritis in hip, knee and/or lumbar spine | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001571-17 | Sponsor Protocol Number: 21-0148 | Start Date*: 2021-08-25 | |||||||||||
Sponsor Name:CHU de Nantes | |||||||||||||
Full Title: | |||||||||||||
Medical condition: refractory lumbosciatic patients | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004775-78 | Sponsor Protocol Number: 1014802-203 | Start Date*: 2016-05-09 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of BIIB074 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
Medical condition: Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Completed) GB (Completed) CZ (Completed) SK (Completed) AT (Completed) ES (Completed) NL (Completed) BE (Completed) FR (Completed) RO (Completed) BG (Completed) LT (Prematurely Ended) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004013-41 | Sponsor Protocol Number: AUH-TFB-SSPS-3 | Start Date*: 2015-09-18 | ||||||||||||||||
Sponsor Name:Thomas Fichnter Bendtsen | ||||||||||||||||||
Full Title: Supra Sacral Parallel Shift - ultrasound/MR image fusion guided lumbosacral plexus block | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005544-33 | Sponsor Protocol Number: AUH-TFB-SR-ULMR | Start Date*: 2016-02-08 | ||||||||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | ||||||||||||||||||
Full Title: Shamrock – Ultrasound/MR image fusion guided lumbar plexus blocks | ||||||||||||||||||
Medical condition: Hip surgery anaesthesia and perioperative analgesia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002119-33 | Sponsor Protocol Number: 2017-02 | Start Date*: 2017-09-07 | |||||||||||
Sponsor Name:ZonMW | |||||||||||||
Full Title: The PLUS study: Preventing LUmbar Disc Surgery | |||||||||||||
Medical condition: Lumbosacral Radicular Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015840-40 | Sponsor Protocol Number: LEVO/HK | Start Date*: 2009-10-19 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Chronic pain and mobility outcomes following primary hip arthroplasty. A comparison of intravenous morphine with lumbar plexus levobupivacaine. | ||
Medical condition: Acute and chronic pain following hip replacement surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-001608-35 | Sponsor Protocol Number: HUM-04-80 | Start Date*: 2006-12-01 | |||||||||||
Sponsor Name:Dr. Valérie gangji | |||||||||||||
Full Title: TREATMENT OF SCIATICA BY ADALIMUMAB INJECTION : A RANDOMIZED, DOUBLE BLIND CONTROLLED TRIAL. | |||||||||||||
Medical condition: To determine the efficacy of adalimumab in disc herniation-induced sciatica in a controlled randomised double blind pilot study. | |||||||||||||
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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: 2006-004317-18 | Sponsor Protocol Number: TAP4 | Start Date*: 2009-06-09 | |||||||||||
Sponsor Name:Dept of Anaesthesia, University College Hospital, Galway | |||||||||||||
Full Title: Comparison of continuous Lumbar Epidural (LEP) and Transversus Abdominis Plane (TAP) Blockade in the management of postoperative pain post abdominal surgery. | |||||||||||||
Medical condition: Postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022025-15 | Sponsor Protocol Number: 10-2-055 | Start Date*: 2011-02-21 |
Sponsor Name:MUMC | ||
Full Title: Intradiscal Methylene Blue Injection Treatment for Chronic Discogenic Low back pain A prospective Clinical Series followed by a Randomised Placebo-Controlled Clinical Trial | ||
Medical condition: The Randomized Clinical Trial (RCT) aims to prove the hypothesis that Intradiscal Methylene blue Injection is capable of better pain reduction than the best available treatment in patients sufferin... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000321-41 | Sponsor Protocol Number: ALENDROHNP2011 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:FUNDACION HOSPITAL NACIONAL DE PARAPLEJICOS PARA LA INVESTIGACIÓN Y LA INTEGRACIÓN | |||||||||||||
Full Title: PREVENTIVE TREATMENT OF BONE MASS LOSS WITH ALENDRONATE AND CALCIFEDIOL IN PATIENTS WITH ACUTE SPINAL CORD INJURY | |||||||||||||
Medical condition: Preventing loss of bone density in patients with spinal cord injury of traumatic etiology complete during the first year of evolution of the lesion. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018600-87 | Sponsor Protocol Number: Peri-Trauma | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA | |||||||||||||
Full Title: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY: COMPARISON OF INTRAVENOUS ANALGESIA AND ONE-SHOT EPIDURAL LUMBAR NERVE BLOCK. | |||||||||||||
Medical condition: POST-OPERATIVE PAIN CONTROL OF PEDIATRIC PATIENTS UNDERWENT ORTHOPEDIC SURGERY | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006664-24 | Sponsor Protocol Number: INVEX-CLIN-IIH-301 | Start Date*: 2023-04-20 | |||||||||||
Sponsor Name:Invex Therapeutics Ltd. | |||||||||||||
Full Title: A Phase III randomised, placebo-controlled, double-blind, multi-centre, clinical trial to determine the efficacy and safety of Presendin in idiopathic intracranial hypertension | |||||||||||||
Medical condition: Idiopathic intracranial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001317-16 | Sponsor Protocol Number: TRAIN_2019 | Start Date*: 2019-10-30 | ||||||||||||||||
Sponsor Name:ErasmusMC | ||||||||||||||||||
Full Title: The TRAIN study: TRAmetinib In Neurofibromatosis type 1 related symptomatic plexiform neurofibromas | ||||||||||||||||||
Medical condition: Adult patients (age >17 years) with (mosaic) NF1 with inoperable symptomatic plexiform neurofibromas | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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