- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Cold Stress.
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EudraCT Number: 2017-000298-35 | Sponsor Protocol Number: NL60593.028.17 | Start Date*: 2017-05-01 |
Sponsor Name:Tilburg University | ||
Full Title: Oxytocin, friendship and dealing with emotions | ||
Medical condition: There are no medical conditions or disease under investigation. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
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: 2009-009096-35 | Sponsor Protocol Number: QGUY/2008/TA-270/-01 | Start Date*: 2009-03-12 | |||||||||||
Sponsor Name:Activus Pharma Co., Ltd | |||||||||||||
Full Title: An open-label, 28-day multiple dose pilot study to evaluate the effects on lung oxidative stress, safety and pharmacokinetics of TA-270 in patients with chronic obstructive pulmonary disease (COPD). | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease. ( COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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: 2005-002976-14 | Sponsor Protocol Number: CRI103143 | Start Date*: 2006-09-27 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: A phase IIa, single-centre, randomised, placebo-controlled, double-blind, three-period crossover exploratory study investigating the effects on gut autonomic responses of single administrations of ... | ||
Medical condition: Irritable Bowel Syndrome (IBS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005534-20 | Sponsor Protocol Number: 05102006 | Start Date*: 2008-01-24 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Effect of Erdosteine on inflammatory and oxidative biomarkers in sputum and exhaled breath in patients with COPD | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) of different severity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003747-75 | Sponsor Protocol Number: EC07/90250 | Start Date*: 2008-04-21 | |||||||||||
Sponsor Name:Servei Pneumologia. Hospital Universitari Son Dureta | |||||||||||||
Full Title: EFECTOS ANTIINFLAMATORIOS DE LA OXIGENOTERAPIA DOMICILIARIA EN PACIENTES CON ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA ANTIINFLAMMATORY EFFECTS OF DOMICILIARY OXYGENTHERAPY IN PATIENTS WITH CHRONIC O... | |||||||||||||
Medical condition: Pacientes con enfermedad pulmonar obstructiva crónica e hipoxemia (Stable chronic obstructive pulmonary disease with hypoxemia) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001805-18 | Sponsor Protocol Number: Emera003 | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:NBMI Science AB | |||||||||||||
Full Title: A randomised, placebo-controlled, blinded, cross-over, pilot study to explore safety and efficacy of NBMI treatment of patients with mild, moderate and severe Chronic Obstructive Pulmonary Disease ... | |||||||||||||
Medical condition: Patients with Chronic Obstructive Pulmonary Disease (COPD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006276-38 | Sponsor Protocol Number: A4471008 | Start Date*: 2007-06-27 | |||||||||||
Sponsor Name:Boehring Ingelheim Pharma Ges mbH, Regional Division Medicine, Regional Centre Vienna | |||||||||||||
Full Title: A 24 week, randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy and safety of 18 MCG of Tiotropium inhalation capsules administered by Handihaler® once-daily plu... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) GB (Completed) BE (Completed) GR (Completed) PT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005484-32 | Sponsor Protocol Number: VN-FT-01 | Start Date*: 2015-05-28 | ||||||||||||||||||||||||||
Sponsor Name:Lund University | ||||||||||||||||||||||||||||
Full Title: Double-blind, randomized placebo controlled study on the effect from cortisone treatment of vestibular neuritis - function, subjective well-being and stress | ||||||||||||||||||||||||||||
Medical condition: Acute vestibular syndrome better known as Vestibular neuritis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000298-20 | Sponsor Protocol Number: CHL.3/01-2016 | Start Date*: 2016-10-18 | |||||||||||
Sponsor Name:Sintetica S.A. | |||||||||||||
Full Title: Comparison of epidural Chloroprocaine 3% and Ropivacaine 0.75% for unplanned Caesarean section in labouring women who have an epidural catheter in situ | |||||||||||||
Medical condition: Local epidural anaesthesia in labouring women who have an epidural catheter in situ and established analgesia and need unplanned Caesarean | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008339-27 | Sponsor Protocol Number: A0081107 | Start Date*: 2009-05-07 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY10017 | |||||||||||||
Full Title: A 17-WEEK, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTI-CENTER TRIAL OF PREGABALIN FOR THE TREATMENT OF CHRONIC CENTRAL NEUROPATHIC PAIN AFTER SPINAL CORD INJURY | |||||||||||||
Medical condition: Chronic Central Neuropathic Pain after Spinal Cord Injury. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
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