- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Quantitative sensory testing.
Displaying page 1 of 3.
EudraCT Number: 2020-001285-11 | Sponsor Protocol Number: P20.XXX | Start Date*: 2021-01-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A Randomized, open label, Non-inferiority trial on the efficacy of Lacosamide versus Duloxetine in Patients with Chemotherapy-induced Polyneuropathy – A strategy trial | ||
Medical condition: Chemotherapy-induced polyneuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001010-13 | Sponsor Protocol Number: escit01 | Start Date*: 2004-10-25 |
Sponsor Name:Dept. of Neurology, Odense University Hospital | ||
Full Title: Escitalopram til behandling af smerter ved polyneuropati En dobbeltblind, randomiseret, placebokontrolleret undersøgelse (Escitalopram as a treatment for painful polyneuropathy: A double-blind, r... | ||
Medical condition: painful polyneuropathy of different origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001450-26 | Sponsor Protocol Number: LAX-01 | Start Date*: 2019-06-28 | |||||||||||
Sponsor Name:Institute for Public Health and Caring Sciences, Uppsala University | |||||||||||||
Full Title: Can the experience of a diminished effect of local anesthetics be verified by an objective test? | |||||||||||||
Medical condition: Local anesthetics for minor or more major procedures such as suturing lacerations, removing skin lesions, operating ingrown toenails, drilling and removing teeth etc. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013706-13 | Sponsor Protocol Number: TOP_LID_DPNP | Start Date*: Information not available in EudraCT |
Sponsor Name:Wilhelminenspital der Stadt Wien | ||
Full Title: ANALGESIC RESPONSE TO TRANSDERMAL LIDOCAINE IN PATIENTS WITH PAINFUL PERIPHERAL DIABETIC NEUROPATHY UNDERLYING DIFFERENT SENSORY PATTERNS | ||
Medical condition: In this study the effect of transdermal lidocaine in patients with painful peripheral diabetic neuropathy will be examined. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023331-42 | Sponsor Protocol Number: IMIOXC | Start Date*: 2010-12-15 | |||||||||||
Sponsor Name:Department of Neurology, Odense University Hospital | |||||||||||||
Full Title: Oxcarbazepine for the treatment of chronic peripheral neuropathic pain: predictors of response - a randomised, double-blind, placebo-controlled clinical trial | |||||||||||||
Medical condition: Chronic peripheral neuropathic pain caused by polyneuropathy, postherpetic neuralgia and traumatic/surgical nerve injury. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004698-86 | Sponsor Protocol Number: AcuZoster Effectiveness2006 | Start Date*: 2008-07-16 | |||||||||||
Sponsor Name:Schmerzambulanz Innenstadt der LMU | |||||||||||||
Full Title: Untersuchung der analgetischen Wirkung der AKupunktur bei Patienten mit Herpes zoster im Vergleich mit einer medikamentösen Standardtherapie- Comparison of acupuncture treatment to medical standard... | |||||||||||||
Medical condition: Patients suffering from pain due to a herpes zoster infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000640-21 | Sponsor Protocol Number: KetCRPS-2 | Start Date*: 2021-11-10 |
Sponsor Name:Center for Pain Medicine, Erasmus MC | ||
Full Title: Long-term pain modulation by intravenous esketamine in Complex Regional Pain Syndrome: a non-inferiority study | ||
Medical condition: Complex Regional Pain Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003688-24 | Sponsor Protocol Number: P12.??? | Start Date*: 2012-12-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Treatment of Complex Regional Pain Syndrome type 1: A randomized placebo controlled double-blind study with ARA 290 | ||
Medical condition: Complex regional pain syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004468-23 | Sponsor Protocol Number: version3.0 | Start Date*: 2020-02-10 |
Sponsor Name:St George's, University of London | ||
Full Title: Comparison of abatacept with tumor necrosis factor inhibitors in the treatment of rheumatoid arthritis pain: A phase IV trial | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000348-14 | Sponsor Protocol Number: NSTATIN | Start Date*: 2014-03-05 |
Sponsor Name:Odense University Hospital, Department of Neurology | ||
Full Title: Statin-treatment and peripheral neuropathy - a randomized clinical trial | ||
Medical condition: Patients with cerebral infarction or transient ischemic attack. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-003933-32 | Sponsor Protocol Number: A092358 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
Full Title: A randomised, blind, placebo controlled crossover study of the influence of the HCN channel-blocker ivabradine on the symptoms of neuropathic pain | |||||||||||||
Medical condition: Neuropathic Pain | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000205-23 | Sponsor Protocol Number: 14012013 | Start Date*: 2013-03-27 | ||||||||||||||||
Sponsor Name:Department of surgery, Herlev Hospital | ||||||||||||||||||
Full Title: The analgesic effects of melatonin: A randomized, placebo-controlled, double-blinded study on healthy volunteers | ||||||||||||||||||
Medical condition: Heat injury in healthy volunteers | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005773-27 | Sponsor Protocol Number: APHP190353 | Start Date*: 2021-03-09 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: BARIcitinib Cognitive Emotional and Neural signaTuRE BARICENTRE | |||||||||||||
Medical condition: Patients with rheumatoid arthritis and indication of baricitinib treatment according to a rheumatologist | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001072-21 | Sponsor Protocol Number: MKN106762 | Start Date*: 2006-08-08 |
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
Full Title: A double-blind placebo-controlled study of the efficacy and safety of the P38 Map Kinase inhibitor SB681323 in patients with neuropathic pain following nerve trauma | ||
Medical condition: Neuropathic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005590-32 | Sponsor Protocol Number: APCP-113 | Start Date*: 2013-02-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A double blind, placebo controlled Phase 2 study comparing the effects of ARA 290 on neuropathic symptoms of patients with type 2 diabetes | ||
Medical condition: Diabetes type 2: neuropathic symptoms | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004007-19 | Sponsor Protocol Number: AV-007-IM | Start Date*: 2006-11-16 | |||||||||||
Sponsor Name:Nycomed Austria GmbH | |||||||||||||
Full Title: A multi-centre, double-blind, placebo-controlled, randomised, parallel group clinical trial to evaluate efficacy and safety of Actovegin® in diabetic type 2 patients with symptomatic diabetic perip... | |||||||||||||
Medical condition: Diabetic Polyneuropathy | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015242-30 | Sponsor Protocol Number: 2009-001 | Start Date*: 2009-11-05 |
Sponsor Name:The Walton Centre for Neurology and Neurosurgery NHS Trust | ||
Full Title: An open study to compare the efficacy of immunoglobulin administered subcutaneoulsy (SCIG) with current best practice in patients with Complex Regional Pain Syndrome (CRPS) | ||
Medical condition: Complex Regional Pain Syndrome (CRPS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003077-26 | Sponsor Protocol Number: IMIVER | Start Date*: 2012-08-13 | |||||||||||
Sponsor Name:Department of Neurology, Odense University Hospital | |||||||||||||
Full Title: Topical lidocaine for the treatment of focal peripheral neuropathic pain: response in relation to pain phenotype | |||||||||||||
Medical condition: Chronic peripheral neuropathic pain caused by postherpetic neuralgia and traumatic/surgical nerve injury | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001218-26 | Sponsor Protocol Number: TRO19622 CL E Q 1204-1 | Start Date*: 2008-06-19 | |||||||||||
Sponsor Name:TROPHOS SA | |||||||||||||
Full Title: A double blind, placebo controlled study of the effect of 330mg QD of TRO19622 in the treatment of Chemotherapy Induced Peripheral Neuropathy. | |||||||||||||
Medical condition: Symptoms of chemotherapy induced peripheral neuropathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003602-26 | Sponsor Protocol Number: CBA106191 | Start Date*: 2007-05-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A double-blind, two-period, placebo controlled cross-over study of the effects of the CB2 agonist GW842166 on pain and sensitisation in patients with osteoarthritis. | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
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. |
