- Trials with a EudraCT protocol (674)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
674 result(s) found for: Complex.
Displaying page 1 of 34.
EudraCT Number: 2010-024510-57 | Sponsor Protocol Number: TRIANT-TE | Start Date*: 2011-03-14 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: Estudio Randomizado, Prospectivo, Controlado, para Comparar la Eficacia y Seguridad de Dos Estrategias Farmacológicas Diferentes sobre la Alteración Neurocognitiva en la Infección por VIH. Estudio ... | |||||||||||||
Medical condition: Alteración neurocognitiva en la infección por VIH. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2016-003741-29 | Sponsor Protocol Number: MARAND-X | Start Date*: 2017-04-05 | ||||||||||||||||
Sponsor Name:A.S.L. TO 2 | ||||||||||||||||||
Full Title: MARAND-X Study: MARaviroc-based Treatment Switch in HIV-positive Patients with HAND: Consequences of Reducing Antiretroviral-associated NeurotoXicity | ||||||||||||||||||
Medical condition: HIV-infection, HIV-associated neurocognitive disorders | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004411-31 | Sponsor Protocol Number: AC-055-308 | Start Date*: 2013-02-01 | |||||||||||
Sponsor Name:ACTELION PHARMACEUTICALS LTD. | |||||||||||||
Full Title: Long term, single-arm, open-label extension study of protocol AC-055-305 to assess the safety, tolerability and efficacy of macitentan in subjects with Eisenmenger Syndrome. | |||||||||||||
Medical condition: Eisenmenger Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) BG (Completed) GB (Completed) DE (Completed) AT (Completed) PT (Completed) ES (Completed) HU (Completed) CZ (Completed) RO (Completed) PL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
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: 2006-004705-26 | Sponsor Protocol Number: CRO529 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Safety and Tolerability of Sildenafil in Patients with Eisenmenger Physiology | |||||||||||||
Medical condition: Eisenmenger Syndrome (pulmonary hypertension due to congenital heart disease) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 2012-003335-33 | Sponsor Protocol Number: AC-055-305 | Start Date*: 2013-02-27 | |||||||||||
Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||
Full Title: A multi-center, double-blind, randomized, placebo-controlled, parallel-group, Phase 3 study to evaluate the effects of macitentan on exercise capacity in subjects with Eisenmenger Syndrome. | |||||||||||||
Medical condition: Eisenmenger Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) BG (Completed) BE (Completed) DE (Completed) PT (Completed) NL (Completed) AT (Completed) ES (Completed) HU (Completed) CZ (Completed) GR (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: 2019-000938-20 | Sponsor Protocol Number: 2019-5172 | Start Date*: 2021-04-15 |
Sponsor Name:Radboudumc | ||
Full Title: Pharmacokinetic study of minocycline in patients with pulmonary nontuberculous mycobacterial disease | ||
Medical condition: Pulmonary disease caused by Mycobacterium avium complex. Mycobacterium avium complex is a nontuberculous mycobacterium. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002805-13 | Sponsor Protocol Number: LTF-304 | Start Date*: 2015-11-27 | |||||||||||
Sponsor Name:bluebird bio, Inc | |||||||||||||
Full Title: Longterm Follow-up of Subjects With Cerebral Adrenoleukodystrophy Who Were Treated With Lenti-D Drug Product | |||||||||||||
Medical condition: Cerebral Adrenoleukodystrophy (CALD) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2011-006283-42 | Sponsor Protocol Number: KAD166 | Start Date*: 2012-04-30 | |||||||||||
Sponsor Name:Dr. Kade Pharmazeutische Fabrik GmbH | |||||||||||||
Full Title: Placebo-controlled double-blind trial investigating the efficacy and tolerability of Posterisan® akut with lidocaine (50 mg/g rectal ointment) in abatement of complaints associated with the anorect... | |||||||||||||
Medical condition: Relief of complaints associated with anorectal symptom complex (pain, burning, itching) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016996-31 | Sponsor Protocol Number: P09-004 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Placebo–Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-O... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2009-017904-95 | Sponsor Protocol Number: P09-005 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: Open-Label Extension Study to Evaluate the Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-Onset Seizures who had Participated in P09-004, a Randomized, Multicenter, Doub... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005440-25 | Sponsor Protocol Number: SP904 | Start Date*: 2009-02-16 | ||||||||||||||||
Sponsor Name:UCB BIOSCIENCES, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Open-label Extension Trial to Assess the Long-term Use of Lacosamide Monotherapy and Safety of Lacosamide Monotherapy and Adjunctive Therapy in Subjects with Partial-onset Seizures | ||||||||||||||||||
Medical condition: Partial-onset seizures (with and without secondary generalization) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IE (Completed) ES (Completed) AT (Completed) DK (Completed) PT (Not Authorised) IT (Completed) FR (Completed) DE (Completed) Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004590-24 | Sponsor Protocol Number: 1949 | Start Date*: 2005-10-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: PHASE II PILOT PROTOCOL OF BONEMARROW STAM CELLS MOBILIZATION BY CYTOCHINE STIMULATION IN PATIENTS WITH COMPLEX ANAL FISTULAS AND/OR RECURRENCES AND/OR ANAL-PERIANAL LOCALIZATIONS OF IBD | |||||||||||||
Medical condition: PATIENTS WITH COMPLEX ANAL FISTULAS AND/OR RECURRENCES AND/OR ANAL-PERIANAL LOCALIZATIONS OF IBD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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 |
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