- Trials with a EudraCT protocol (58)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
58 result(s) found for: Raynaud's Disease.
Displaying page 1 of 3.
EudraCT Number: 2007-000397-23 | Sponsor Protocol Number: SLx-2101-07-04 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:Surface Logix, Inc. | |||||||||||||
Full Title: A randomised, double blind, placebo-controlled, cross-over pilot study to examine the safety, tolerability and pharmacodynamic profile of repeat oral doses of SLx-2101 once daily for up to 14 days ... | |||||||||||||
Medical condition: Raynaud's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001899-38 | Sponsor Protocol Number: BAY63-2521/16787 | Start Date*: 2013-07-29 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Single dose, double-blind, placebo-controlled, single center, randomized cross-over study to investigate safety, tolerability, pharmacodynamics and pharmacokinetic properties of BAY 63-2521 after o... | |||||||||||||
Medical condition: Patients with 1° and 2° Raynaud’s phenomenon (RP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000309-10 | Sponsor Protocol Number: CHUBX2017/45 | Start Date*: 2021-10-04 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Phase II/III double-blind randomized placebo-controlled trial assessing the preventive effect of Clopidogrel on the systemic sclerosis development risk in subjects with specific dysimmunity and Ray... | |||||||||||||
Medical condition: Raynaud phenomenon | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013468-37 | Sponsor Protocol Number: Protocol code BA7 | Start Date*: 2010-09-29 | ||||||||||||||||
Sponsor Name:Royal National Hospital for Rheumatic Disease | ||||||||||||||||||
Full Title: A short-term open-label single site pilot study evaluating the use of asasantin retard therapy in the management of Raynaud’s phenomenon. | ||||||||||||||||||
Medical condition: Primary Raynaud's Phenomenon and Systemic Sclerosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019009-40 | Sponsor Protocol Number: A7331010 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: Estudio clínico de Fase 2A, multicéntrico aleatorizado, doble ciego, controlado con placebo y con un fármaco activo, de diseño cruzado con dos cohortes y dos dosis, para la evaluación de la eficaci... | |||||||||||||
Medical condition: Tratamiento del vasospasmo en el fenómeno de Raynaud primario y secundario. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) CZ (Completed) DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024005-13 | Sponsor Protocol Number: 3098009 | Start Date*: 2011-03-11 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
Full Title: Efficacy of ORM-12741 for prevention of cold-induced vasospasm; a randomised, double-blind, placebo-controlled, single centre crossover study in patient with Raynaud's phenomenon secondary to syste... | |||||||||||||
Medical condition: Raynaud's phenomenon secondary to systemic sclerosis (Raynaud's syndrome) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003203-35 | Sponsor Protocol Number: VP-C21-004 | Start Date*: 2019-12-13 | ||||||||||||||||
Sponsor Name:Vicore Pharma AB | ||||||||||||||||||
Full Title: A Phase 2, single-center, randomised, double-blind, placebo-controlled, cross-over, cold challenge study investigating the effect of C21 on cold-induced vasoconstriction in subjects with Raynaud’s ... | ||||||||||||||||||
Medical condition: Systemic sclerosis (SSc) Raynaud’s phenomenon (RP) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002081-13 | Sponsor Protocol Number: GS-2001 | Start Date*: 2020-09-08 | ||||||||||||||||
Sponsor Name:Gesynta Pharma AB | ||||||||||||||||||
Full Title: A Phase II, randomised, multi-centre placebo-controlled, double-blind study to investigate the safety of GS-248, and efficacy on Raynaud’s phenomenon (RP) and peripheral vascular blood flow in pati... | ||||||||||||||||||
Medical condition: Raynaud's phenomenon (RP) in patients with Systemic sclerosis (SSc) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018194-31 | Sponsor Protocol Number: PIL001 | Start Date*: 2010-11-03 |
Sponsor Name:Pharmarama International Limited | ||
Full Title: Topical Amlodipine in Raynaud's Phenomenon | ||
Medical condition: The medical conditions under investigation in this trial are as follows: 1] Primary Raynaud's Phenomenon 2] Systemic Sclerosis (SSc) - otherwise known an Seconday Raynaud's Phenomenon. Raynaud's ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000295-41 | Sponsor Protocol Number: Ro-002/05 | Start Date*: 2006-05-29 |
Sponsor Name:Universität zu Köln | ||
Full Title: Double-blind,placebo-controlled cross-over study for evaluation of the efficacy of the PDE-5-inhibitor vardenafil on the peripheral perfusion and the clinical symptomatology of patients with Raynau... | ||
Medical condition: Raynaud´s disease (RD) is defined as episodic, painful, cold- or emotional stress-triggered vasospasms of the digital arteries and precapillary arterioles for up to 30 minutes with or without under... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004596-12 | Sponsor Protocol Number: 110905 | Start Date*: 2014-01-22 |
Sponsor Name:Azienda ospedaliera universitaria Ospedali Riuniti | ||
Full Title: HOME INFUSION THERAPY WITH ILOPROST USING A PORTABLE SYRINGE PUMP FOR THE TREATMENT OF PERIPHERAL ULCERS AND RAYNAUD'S PHENOMENON IN SYSTEMIC SCLEROSIS. | ||
Medical condition: Raynaud's phenomenon and acral ulcers in systemic sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019977-14 | Sponsor Protocol Number: CILOS-RAY2010 | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA SAN MARTINO GENOVA | |||||||||||||
Full Title: Efficacy of Cilostazol for the treatment of Raynaud’s Phenomenon in patients affected by Systemic Sclerosis | |||||||||||||
Medical condition: Patients affected by Systemic Sclerosis with Raynaud’s Phenomenon | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002984-32 | Sponsor Protocol Number: FER-COM-16-004 | Start Date*: 2017-02-16 | |||||||||||
Sponsor Name:UNIVERSITÀ CATTOLICA DEL SACRO CUORE- POLICLINICO A. GEMELLI | |||||||||||||
Full Title: Treatment of the Reynaud's Disease associated with ischemic ulcers in patients affected by sistemic sclerosis | |||||||||||||
Medical condition: SISTEMIC SCLEROSIS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005723-20 | Sponsor Protocol Number: RC31/20/0445 | Start Date*: 2022-02-10 |
Sponsor Name:CHU de Toulouse | ||
Full Title: Evaluation of Botulinum TOXin type A in the treatment of Buerger’s disease | ||
Medical condition: This study assesses the feasibility and safety of treatment with botulinum toxin injection in patients with Buerger's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001719-65 | Sponsor Protocol Number: CALC-SSc | Start Date*: 2018-12-10 |
Sponsor Name:University Medial Center Groningen | ||
Full Title: CALCification as an early marker of vasculopathy and organ involvement in Systemic Sclerosis CALC-SSc study | ||
Medical condition: Systemic sclerosis (SSc) is a rare progressive autoimmune disease hallmarked by severe vasculopathy. Patients are prone to enhanced calcification of skin and the vasculature. Active calcifications ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001617-27 | Sponsor Protocol Number: IVA_01_337_HSSC_15_001 | Start Date*: 2015-09-18 | ||||||||||||||||
Sponsor Name:Inventiva SAS | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicentre proof-of-concept trial of IVA337 in the treatment of diffuse cutaneous systemic sclerosis | ||||||||||||||||||
Medical condition: Systemic sclerosis (scleroderma) (SSc) is a chronic connective tissue disorder of unknown aetiology characterized by widespread microvascular damage and excessive deposition of collagen in the skin... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) ES (Completed) GB (Completed) DE (Completed) NL (Completed) SI (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001101-40 | Sponsor Protocol Number: 13/0417 | Start Date*: 2015-02-24 | ||||||||||||||||
Sponsor Name:University College London (UCL) | ||||||||||||||||||
Full Title: Sclero XIII: A phase II ,double-blind, randomized, placebo-controlled study to investigate pharmacokinetics (PK), safety and efficacy of intravenous factor XIII treatment in patients with systemic... | ||||||||||||||||||
Medical condition: Systemic Sclerosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001817-33 | Sponsor Protocol Number: GLPG1690-CL-204 | Start Date*: 2019-01-14 | |||||||||||
Sponsor Name:Galapagos NV | |||||||||||||
Full Title: A Phase 2a randomized, double-blind, placebo-controlled, multi-center study to evaluate the efficacy, safety, and tolerability of orally administered GLPG1690 for 24 weeks in subjects with systemic... | |||||||||||||
Medical condition: Systemic sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005230-20 | Sponsor Protocol Number: NOT AVAILABLE | Start Date*: 2006-07-14 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: EX VIVO EFFECT OF AMINAFTONE (CAPILLAREMA) ON THE ENDOTELIAL FUNCTION IN SYSTEMIC SCLEROSIS. Effetto ex vivo dell’aminaftone (Capillarema) sulla funzione endoteliale nella Sclerosi Sistemica | |||||||||||||
Medical condition: Variazione della gravita' del fenomeno di Raynaud misurata mediante diario dei sintomi e scala analogica visiva VAS ヨ Visual Analogic Scale (6). Variazione dello stato globale di malattia valutat... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004937-19 | Sponsor Protocol Number: CMHV370A12201 | Start Date*: 2021-09-08 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A multi-center, randomized, participant- and investigator- blinded, placebo-controlled, parallel group basket study to evaluate the safety, tolerability and efficacy of MHV370 in participants with ... | ||||||||||||||||||
Medical condition: Sjögren’s syndrome Mixed connective tissue disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) HU (Completed) | ||||||||||||||||||
Trial results: View results |
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