- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (502)
8 result(s) found for: TENS.
Displaying page 1 of 1.
EudraCT Number: 2004-002531-32 | Sponsor Protocol Number: GWCL0405 | Start Date*: 2005-07-28 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A double blind, randomised, placebo controlled, parallel group study of Sativex, in the treatment of subjects with peripheral neuropathic pain associated with allodynia | ||
Medical condition: Peripheral neuropathic pain associated with allodynia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) CZ (Completed) BE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002530-20 | Sponsor Protocol Number: GWCL0305 | Start Date*: 2005-04-29 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A double blind, randomised, placebo controlled, parallel group study of Sativex in the treratment of subjects with pain due to diabetic neuropathy | ||
Medical condition: Painful diabetic neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000269-36 | Sponsor Protocol Number: HIPAIN | Start Date*: 2018-05-23 |
Sponsor Name:JORGE ORDUÑA VALLS | ||
Full Title: Randomized clinical trial to evaluate the efficacy of two techniques against chronic hip pain: cooled radiofrequency over sensitive nerves of the hip, compared to intraarticular injection of steroi... | ||
Medical condition: Chronic Hip Pain by Osteoarthrosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002563-41 | Sponsor Protocol Number: RFCLAI004 | Start Date*: 2016-02-09 | |||||||||||
Sponsor Name:Jorge Orduna Valls | |||||||||||||
Full Title: Prospective, randomized cohort study to evaluate the efficacy of two techniques against chronic knee pain: echo-guided radiofrequency over sensitive nerves of the knee, compared to intraarticular i... | |||||||||||||
Medical condition: Chronic knee pain (more than 3 months), in patients either non eligible for knee surgery, or with pain after three months of knee surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2004-000414-39 | Sponsor Protocol Number: BUP4203 | Start Date*: 2004-08-10 | |||||||||||
Sponsor Name:Mundipharma OY | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the long-term efficacy and safety of Norspan® versus placebo Norspan in subjects with chronic, moderate... | |||||||||||||
Medical condition: Chronic, moderate to severe osteoarthritis pain of the hip and/or knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003544-83 | Sponsor Protocol Number: 69HCL19_0375 | Start Date*: 2021-03-16 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique | ||||||||||||||||||
Full Title: Evaluation de l’efficacité thérapeutique du filgrastim dans les allergies sévères bulleuses aux médicaments s’exprimant sous forme de Lyell et Stevens-Johnson Etude GNET | ||||||||||||||||||
Medical condition: Syndrome de Stevens Johnson (SJS) Syndrome de Lyell (NET) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005061-20 | Sponsor Protocol Number: ONU3705 | Start Date*: 2012-06-19 | ||||||||||||||||
Sponsor Name:Purdue Pharma L.P. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Double-dummy, Placebo-controlled, Active-controlled, Parallel-group, Multicenter Trial of Oxycodone/Naloxone Controlled-release Tablets (OXN) to Assess the Analgesic Eff... | ||||||||||||||||||
Medical condition: Opioid-induced Constipation & Moderate to Severe Chronic Low back Pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) SK (Completed) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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