- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: N-acetylcysteine (NAC).
Displaying page 2 of 2.
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EudraCT Number: 2007-003643-71 | Sponsor Protocol Number: 2007rc09JOB | Start Date*: 2008-08-25 | ||||||||||||||||
Sponsor Name:Direction Centrale du Service de Santé des Armées (DCSSA) | ||||||||||||||||||
Full Title: Evaluation chez l'homme de l'effet otoprotecteur de la N-Acetyl-Cysteine par voie orale en prévention des effets délétères de l'exposition au bruit impulsionnel | ||||||||||||||||||
Medical condition: chemical prevention of permanent Noise-Induced-Hearing loss (NIHL) in Army personel that use firearms | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004188-35 | Sponsor Protocol Number: CCM1140 | Start Date*: 2020-10-07 | |||||||||||
Sponsor Name:CENTRO CARDIOLOGICO SPA FONDAZIONE MONZINO | |||||||||||||
Full Title: Time-dependent activity of N-acetylcysteine on plasma antioxidant capacity in subjects with redox unbalance-Studio CAPITAL | |||||||||||||
Medical condition: ARTERIAL HYPERTENSION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000564-14 | Sponsor Protocol Number: PIPF-023 | Start Date*: 2013-06-18 | |||||||||||
Sponsor Name:InterMune International AG. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study of the Safety and Tolerability of N–Acetylcysteine in Patients with Idiopathic Pulmonary Fibrosis with Background Treatment of Pirfenid... | |||||||||||||
Medical condition: Patients with Idiopathic Pulmonary Fibrosis (IPF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) DE (Completed) IT (Completed) AT (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004463-44 | Sponsor Protocol Number: CHUB-NAC | Start Date*: 2020-01-22 | |||||||||||
Sponsor Name:CHU Saint Pierre | |||||||||||||
Full Title: Intratympanic injection of N-acetylcysteine for prevention of Cisplatine-induced ototoxicity | |||||||||||||
Medical condition: Ototoxicity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000420-34 | Sponsor Protocol Number: CHUB-NAC-Craving | Start Date*: 2018-11-27 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire Brugmann | |||||||||||||
Full Title: Efficacy of N-acetylcysteine on the craving symptoms of hospitalized patients with cocaine addiction. | |||||||||||||
Medical condition: Cocaine addiction | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001995-12 | Sponsor Protocol Number: CCM1006 | Start Date*: 2019-09-27 | |||||||||||
Sponsor Name:CENTRO CARDIOLOGICO SPA FONDAZIONE MONZINO | |||||||||||||
Full Title: Cardiac Arrhythmia catheter ablation procedures guided by x-Ray imaging: N-Acetylcysteine Protection Against radiation induced Cellular damagE (CARAPACE Study). | |||||||||||||
Medical condition: Patients with Cardiac Arrhythmia who undergo catheter ablation procedures guided by x-Ray imaging | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000955-90 | Sponsor Protocol Number: renac | Start Date*: 2007-04-24 | |||||||||||
Sponsor Name:ISTITUTO C. MONDINO | |||||||||||||
Full Title: Randomized, single-blind, clinical and MRI study for evaluation of safety and efficacy of N-Acetyl Cysteine (NAC) associated with high-dose beta-Interferon in Relapsing-Remitting (RR) multiple scl... | |||||||||||||
Medical condition: multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006815-62 | Sponsor Protocol Number: NAC/CT/2006. | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:University Hospitals of South Manchester NHS Foundation Trust | |||||||||||||
Full Title: Does N-Acetylcysteine (Parvolex) prophylaxis reduce the incidence of renal impairment after on pump Coronary artery bypass surgery? A prospective randomised controlled trial. | |||||||||||||
Medical condition: Renal impairment after coronary artery byapass surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001097-24 | Sponsor Protocol Number: PHT/2013/01 | Start Date*: 2013-05-23 | |||||||||||
Sponsor Name:Portsmouth Hospitals NHS trust | |||||||||||||
Full Title: Use of N-Acetylcysteine (NAC) and Simeticone as a pre-endoscopic drink to improve mucosal visualisation during gastroscopy: A randomised controlled trial | |||||||||||||
Medical condition: Early gastrointestinal lesions in the upper gastrointestinal tract. Our study is not looking at the direct treatment of any particular condition, but the early detecton of lesions. When performin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004613-10 | Sponsor Protocol Number: IRIVITC2008 | Start Date*: 2008-09-12 | ||||||||||||||||
Sponsor Name:University College Hospital Galway | ||||||||||||||||||
Full Title: The role of the antioxidants ascorbic acid and n-acetylcysteine in the attenuation of ischaemia reperfusion injury in a human model | ||||||||||||||||||
Medical condition: Ischaemia reperfusion injury | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004483-22 | Sponsor Protocol Number: 35664 | Start Date*: 2013-11-29 | |||||||||||
Sponsor Name:Mental Health Service, Esbjerg | |||||||||||||
Full Title: NACOS - The effect of N-acetylcystein for depressive symptoms in patients with bipolar depression - A double blind randomized placebo-controlled trial with follow up | |||||||||||||
Medical condition: Bipolar depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006549-42 | Sponsor Protocol Number: EN3285-302 | Start Date*: 2008-06-11 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Multinational, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of EN3285 for the Prevention or Delay to Onset of Severe Oral Mucositis in Subjects wi... | |||||||||||||
Medical condition: Severe Oral Mucositis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005889-40 | Sponsor Protocol Number: ABR-15108 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: N-Acetylcysteine for Treatment of Sickle Cell Disease | |||||||||||||
Medical condition: Patients homozygous for sickle cell disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022994-32 | Sponsor Protocol Number: 34009 | Start Date*: 2011-06-24 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: Effect of N-acetylcysteine on hydrogen sulfide in chronic kidney disease | ||||||||||||||||||
Medical condition: Chronic kidney disease End stage renal disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003360-37 | Sponsor Protocol Number: 1199.247 | Start Date*: 2017-02-28 |
Sponsor Name:Boehringer Ingelheim | ||
Full Title: A double blind, randomized, placebo-controlled trial evaluating the efficacy and safety of nintedanib over 52 weeks in patients with Progressive Fibrosing Interstitial Lung Disease (PF-ILD) | ||
Medical condition: The aim of the current study is to investigate the efficacy and safety of 150 mg bid nintedanib over 52 weeks in patients with Progressive Fibrosing Interstitial Lung Disease (PF-ILD) defined as pa... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) ES (Completed) BE (Completed) DE (Completed) GB (Completed) PL (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002670-39 | Sponsor Protocol Number: PROXI2017 | Start Date*: 2018-02-01 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Bispebjerg Hospital | ||||||||||||||||||||||||||||||||||||||
Full Title: Hyperoxia and antioxidant intervention during major non-cardiac surgery and risk of cerebral and cardiovascular complications, a blinded 2x2 factorial randomized clinical trial | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing major non-cardiac surgery | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003076-22 | Sponsor Protocol Number: PSY-201401_ESPRIT | Start Date*: 2016-07-07 | ||||||||||||||||
Sponsor Name:Central Institute of Mental Health Mannheim (ZI) | ||||||||||||||||||
Full Title: Multimodal Prevention of First Psychotic Episode – a 2x2-Factorial Randomized Trial investigating the efficacy of Acetylcysteine (ACC) and Integrated Preventive Psychological Intervention (IPPI) in... | ||||||||||||||||||
Medical condition: Clinical High Risk state for developing a first psychotic episode | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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