8 result(s) found for: Spondylolisthesis.
Displaying page 1 of 1.
| EudraCT Number: 2015-000072-99 | Sponsor Protocol Number: 05012015 | Start Date*: 2015-05-06 | |||||||||||||||||||||
| Sponsor Name:Ilkka Helenius | |||||||||||||||||||||||
| Full Title: EFFECT OF PREGABALIN ON IMMEDIATE POSTOPERATIVE AND LONGTERM PAIN AND SPINAL MONITORING IN CHILDREN UNDERGOING INSTRUMENTED SPINAL SURGERY. A placebo-controlled randomized clinical trial | |||||||||||||||||||||||
| Medical condition: Idiopatic scoliosis | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-002642-23 | Sponsor Protocol Number: NVD-CLN01 | Start Date*: 2016-11-28 |
| Sponsor Name:Novadip Biosciences | ||
| Full Title: A prospective multi-centre, randomised, controlled study to evaluate the safety and preliminary effectiveness of NVD-001 for the treatment of low grade degenerative lumbar spondylolisthesis by inte... | ||
| Medical condition: Patients diagnosed with symptomatic degenerative spondylolisthesis grade I or II with an indication for spinal fusion of one vertebral segment (L1-S1). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) PL (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005766-36 | Sponsor Protocol Number: | Start Date*: 2006-11-17 |
| Sponsor Name:Sofamor - Danek | ||
| Full Title: A Randomized Prospective Study of Instrumented Posterior Lumbar Interbody Fusion: Autologous Iliac Crest Bone Graft vs. Inductos™ | ||
| Medical condition: We will investigate if the use of Inductos in a intervertebral cage will provide us with better and or faster fusion rates. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-000675-34 | Sponsor Protocol Number: EU 101 | Start Date*: 2004-12-21 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: A Prospective, Randomized, Controlled, Multi-center, (Pilot) Study of Osigraft® in Instrumented Posterolateral Fusions | ||
| Medical condition: Subjects qualifying for decompression and fusion of one spinal level (L3-S1) with the use of autograft will be recruited through the medical institutions of participating investigators. All subject... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001146-29 | Sponsor Protocol Number: 1 | Start Date*: 2016-01-12 |
| Sponsor Name:Hospital Central de la Defensa | ||
| Full Title: Selective local anesthesia versus a combined medication injection with corticosteroids in degenerartive spine | ||
| Medical condition: Degenerative spine pain when there are no indications for surgical treatment | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-002426-10 | Sponsor Protocol Number: OXN4502 | Start Date*: 2008-12-19 |
| Sponsor Name:Napp Pharmaceuticals Ltd | ||
| Full Title: A double-blind, double-dummy, parallel group, randomised study to compare the efficacy and tolerability of oxycodone/naloxone prolonged release (OXN PR) and codeine/paracetamol in the treatment of... | ||
| Medical condition: Moderate to severe chronic lowback pain or pain due to osteoarthritis of the hip and/or knee. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000860-14 | Sponsor Protocol Number: GR-OG-279239-03 | Start Date*: 2018-02-27 | |||||||||||
| Sponsor Name:Genera Research Ltd | |||||||||||||
| Full Title: Patient and evaluator blinded non-inferiority study on safety, tolerability and lumbar fusion efficacy of a single administration of Osteogrow (rhBMP6 in autologous blood coagulum (ABC) carrier) in... | |||||||||||||
| Medical condition: Lumbar spine single segment destabilization caused by degenerative disc disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003752-19 | Sponsor Protocol Number: OXN3401 | Start Date*: 2005-02-01 | |||||||||||
| Sponsor Name:Mundipharma Research GmbH & Co.KG | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo- and Active-controlled, Double-dummy, Parallel Group Study to Determine the Safety and Efficacy of Oxycodone/Naloxone Prolonged-release Tablets in Subjects with ... | |||||||||||||
| Medical condition: Moderate to severe chronic pain of low back that requires around-the-clock opioid therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) DK (Completed) SK (Completed) ES (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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