- Trials with a EudraCT protocol (11)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11 result(s) found for: Lumbar spinal stenosis.
Displaying page 1 of 1.
EudraCT Number: 2011-006152-36 | Sponsor Protocol Number: 1774 | Start Date*: 2012-05-10 | |||||||||||
Sponsor Name:Middelfart Rygsektor | |||||||||||||
Full Title: Postoperative treatment with parathyroidea hormone Forteo® in patients undergoing posterolateral spinal fusion surgery. A prospektive and a randomized double-blinded, placebo-controlled study | |||||||||||||
Medical condition: Spinal stenosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002887-14 | Sponsor Protocol Number: 2.0 | Start Date*: 2016-10-31 | |||||||||||
Sponsor Name:University of Turku | |||||||||||||
Full Title: Dose response study of Patient Controlled Analgesia (PCA) of S-ketamine in orthopaedic spine surgery patients | |||||||||||||
Medical condition: Patients who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003252-31 | Sponsor Protocol Number: 2.0 | Start Date*: 2015-05-15 | |||||||||||
Sponsor Name:University of Turku | |||||||||||||
Full Title: Dose response study of Patient Controlled Analgesia (PCA) of Dexmedetomidine in orthopaedic spine surgery patients | |||||||||||||
Medical condition: Patients, who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000747-26 | Sponsor Protocol Number: KETTO201200047426 | Start Date*: 2012-04-27 | |||||||||||
Sponsor Name:Helsinki Universiy Central Hospital | |||||||||||||
Full Title: Administration of S-Ketamine during spinal surgery to reduce postoperative pain | |||||||||||||
Medical condition: adult patients undergoing spinal surgery | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
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: 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: 2013-001160-38 | Sponsor Protocol Number: lidocaineplif | Start Date*: 2014-01-08 | |||||||||||||||||||||
Sponsor Name:ZNA Middelheim | |||||||||||||||||||||||
Full Title: Impact of intravenous lidocaine infusion on postoperative analgesia for one or two level posterior lumbar interbody fusion surgery | |||||||||||||||||||||||
Medical condition: The postoperative pain intensity after posterior interbody fusion surgery is often intense and difficult to treat with IV morphine and paracetamol alone. Besides, the use of opioids is often associ... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002694-37 | Sponsor Protocol Number: 507A011 | Start Date*: 2016-09-01 |
Sponsor Name:Kuopio University hospital | ||
Full Title: Dexmedetomidine infusion in pain management during low back surgery Dexmedetomidine is an alpha-2-adrenergic agonist that is used mainly for sedation in the intensive care unit. Alpha-2-adre... | ||
Medical condition: Low back pain, Discus prolapse, Spinal stenosis | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002948-10 | Sponsor Protocol Number: A0081007 | Start Date*: 2005-07-14 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: A Randomised Placebo-Controlled Trial of the Efficacy and Safety of Pregabalin in the Treatment of Subjects with Neuropathic Pain Associated with Lumbo-sacral Radiculopathy (protocol dates 2004-11... | |||||||||||||
Medical condition: Pain associated with lumbo-sacral radiculopathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
