- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Complex Regional Pain Syndrome.
Displaying page 1 of 2.
EudraCT Number: 2008-005783-14 | Sponsor Protocol Number: 830423-2008 | Start Date*: 2008-12-16 | |||||||||||
Sponsor Name:Adj,Professor, Torsten Gordh | |||||||||||||
Full Title: En proof of concept (POC) studie gällande guanethidines smärtlindrande effekt vid regional i.v administrering för behandling av komplext regional smärtsyndrom (CRP) | |||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS) är namnet på det smärtsamma tillstånd som kan utvecklas i en fot eller hand efter en skada. Det kan till exempel vara en skada i form av ett brutet ben eller e... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001164-11 | Sponsor Protocol Number: KF7013-03 | Start Date*: 2017-04-24 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Open-label safety trial of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS) | ||||||||||||||||||
Medical condition: Complex regional pain syndrome (CRPS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004664-23 | Sponsor Protocol Number: ST 200 DS 05-01 | Start Date*: 2006-05-25 | |||||||||||
Sponsor Name:SIGMA-TAU | |||||||||||||
Full Title: The role of Acetyl-L-Carnitine in Reflex Sympathetic Dystrophy RDS and in Complex Regional Pain Syndrome CRPS .Pilot clinical trial. | |||||||||||||
Medical condition: Reflex Sympathetic Dystrophy RDS and Complex Regional Pain Syndrome CRPS . | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004750-21 | Sponsor Protocol Number: TAK-935-2008 | Start Date*: 2019-06-10 | ||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, a wholly owned subsidiary of Takeda | ||||||||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-935 as an Adjunctive Therapy in Adult Subjects With Chronic Complex Regional... | ||||||||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003833-91 | Sponsor Protocol Number: KF7013-02 | Start Date*: 2018-10-04 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial investigating the efficacy and safety of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS) | ||||||||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010557-12 | Sponsor Protocol Number: Version1.0/Jan2009 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:The Pennine Acute Hospitals NHS Trust | |||||||||||||
Full Title: A Single Blind, Randomised, Cross-over Study to Compare the Efficacy of Lidocaine 5% Plasters(Versatis) versus Pregabalin (Lyrica) in the Treatment of Complex Regional Pain Syndrome, Type 1. | |||||||||||||
Medical condition: Complex regional pain syndrome type 1. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2014-001915-37 | Sponsor Protocol Number: KF7013-01 | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, double-blind trial investigating the efficacy and safety of intravenous neridronic acid in subjects with complex regional pain syndrome type I (CRPS-I) | |||||||||||||
Medical condition: Complex regional pain syndrome type I (CRPS-I) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024558-12 | Sponsor Protocol Number: CRPS-1-2011-2014 | Start Date*: 2011-02-17 | |||||||||||
Sponsor Name:Aalto-yliopiston Kylmälaboratorion Aivotutkimusyksikkö | |||||||||||||
Full Title: CRPS-potilaiden aivomuutosten korjaantuminen hoidon myötä | |||||||||||||
Medical condition: Complex regional pain syndrome tyyppi 1 eli CRPS-I -potilaita | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019997-33 | Sponsor Protocol Number: 2010/03 | Start Date*: 2010-06-02 | ||||||||||||||||
Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
Full Title: Responsiveness to botulinum toxinum type A in complex regional pain syndrome related fixed dystonia | ||||||||||||||||||
Medical condition: CRPS with dystonia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007794-23 | Sponsor Protocol Number: PAINLESS | Start Date*: 2009-05-28 | |||||||||||
Sponsor Name:Justus-Liebig-University | |||||||||||||
Full Title: Prospektive, doppelblinde, randomisierte, Plazebo-kontrollierte Cross-over Studie zur Wirkung von intravenösen Immunglobulinen bei komplex-regionalem Schmerzsyndrom Typ I (M. Sudeck) | |||||||||||||
Medical condition: complex-regional pain syndrome type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000411-10 | Sponsor Protocol Number: 4478944789 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
Sponsor Name:BG-Kliniken Bergmannsheil, Dept. of Pain Management | |||||||||||||||||||||||||||||||||
Full Title: Effects of Pregabalin on mechanical hyperalgesia - EPOM | |||||||||||||||||||||||||||||||||
Medical condition: patients with pain for at least 6 months and hyperalgesia with one of the following diagnoses: peripheral nerve lesion, plexus lesion, radicular lesion, spinal lesion, polyneuropathy, postzosteric ... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019891-54 | Sponsor Protocol Number: WC2010-022 | Start Date*: 2010-08-10 |
Sponsor Name:VU University Medical Center | ||
Full Title: Effects of oral corticosteroids and DMSO on inflammatory signs and symptoms in Complex Regional Pain Syndrome type 1 | ||
Medical condition: Complex regional pain syndrome type 1. This condition is a pain syndrome with unknown pathophysiology. Research shows that inflammation plays a role in the development and course of the disease. Ev... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001527-22 | Sponsor Protocol Number: AXS02-301 | Start Date*: 2015-09-25 | |||||||||||
Sponsor Name:Axsome Therapeutics, Inc. | |||||||||||||
Full Title: CREATE-1 Study: CRPS Treatment Evaluation 1 Study. A Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of AXS-02 (Disodium Zoledronate Tetrahydrate) Administered ... | |||||||||||||
Medical condition: Complex regional pain syndrome (CRPS-I). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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: 2015-000145-24 | Sponsor Protocol Number: PI2015_843_0001 | Start Date*: 2015-09-21 | |||||||||||
Sponsor Name:CHU Amiens - Picardie | |||||||||||||
Full Title: Role of Vitamin C at 6 Months on Incidence of Complex Regional Pain Syndrome Type I in Upper Limb Surgery (CRPS-VITC) | |||||||||||||
Medical condition: Algoneurodystrophy CRPS type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005557-24 | Sponsor Protocol Number: 69HCL18_0996 | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Hospices Civils de Lyon - Direction de la Recherche Clinique et de l'Innovation | |||||||||||||
Full Title: Étude pilote visant à évaluer l’efficacité d’un mélange de kétamine/lidocaïne administré par mésothérapie dans la prise en charge des douleurs neuropathiques du Syndrome Douloureux Régional Complex... | |||||||||||||
Medical condition: Complex regional pain syndrome type I | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001353-41 | Sponsor Protocol Number: NL56714.029.16 | Start Date*: 2016-06-06 |
Sponsor Name:VU University medical center Amsterdam | ||
Full Title: Oxygenation of Affected Limbs in CRPS-I Patients | ||
Medical condition: Complex Regional Pain Syndrome, Neuropathic Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
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: 2017-004244-37 | Sponsor Protocol Number: KF7013-04 | Start Date*: 2018-08-16 | ||||||||||||||||
Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
Full Title: Placebo-controlled efficacy and safety trial of intravenous neridronic acid in subjects with complex regional pain syndrome (CRPS) | ||||||||||||||||||
Medical condition: Complex Regional Pain Syndrome (CRPS) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) SK (Completed) | ||||||||||||||||||
Trial results: View results |
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