- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Reactive oxygen species.
Displaying page 1 of 2.
EudraCT Number: 2009-009036-77 | Sponsor Protocol Number: PARIBU - 024 | Start Date*: Information not available in EudraCT |
Sponsor Name:Section of dental pharmacology and pharmacotherapy, ICO, University of Oslo | ||
Full Title: THE EFFECT OF IBUPROFEN AND PARACETAMOL ON REACTIVE OXYGEN SPECIES (ROS) IN LEUKOCYTES. | ||
Medical condition: Radical oxygen activity in leukocytes. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003962-10 | Sponsor Protocol Number: DOA_HO | Start Date*: 2015-12-10 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of Hyperoxia on Haemostasis, Inflammation and oxidative Stress | ||
Medical condition: Effects of hyperoxia on haemostasis, inflammation and reactive oxygen species | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004406-10 | Sponsor Protocol Number: 000 | Start Date*: 2013-10-09 |
Sponsor Name:University Hospital Hradec Kralove | ||
Full Title: The use of oxygen and hydrogen mixture for inhalation to prevent ischaemia-reperfusion injury | ||
Medical condition: The patients suffering form acute transmural myocardial infarction and treated with percutaneous transluminal coronary angioplasty will be included in the study. After the recanalisation of occlude... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013228-21 | Sponsor Protocol Number: | Start Date*: 2010-07-06 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Prevention of atrial oxidative stress and electrical remodelling in patients undergoing cardiac surgery: randomised placebo-controlled trial of perioperative high-dose atorvastatin | |||||||||||||
Medical condition: POST-OPERATIVE ATRIAL FIBRILLATION | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001584-36 | Sponsor Protocol Number: 2014-03-11 | Start Date*: 2016-06-01 |
Sponsor Name:Universitetssjukhuset Örebro | ||
Full Title: Is high oxygen concentration a riskfactor for postoperative complications? A prospective, randomized, singel blinded study in elderly patients undergoing vascular surgery | ||
Medical condition: Elective vascular surgery (peripheral vascular and aortic surgery) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003680-38 | Sponsor Protocol Number: HDVitC | Start Date*: 2015-06-12 |
Sponsor Name:VU university medical center | ||
Full Title: Pharmacokinetics of two different high dose regimes of intravenous vitamin C in critically ill patients | ||
Medical condition: Critically ill patients with trauma or sepsis exhibit a high degree of vitamin C deficiency at ICU admission and vitamin C plasma concentrations decrease even more during the first three days of ad... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016738-28 | Sponsor Protocol Number: ALISEI | Start Date*: 2009-12-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Phase IV prospective, randomized, open with blind endpoints, parallel group study to evaluate the effect of Aliskiren on endothelial dysfunction in patients with essential hypertension | |||||||||||||
Medical condition: essential hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001971-61 | Sponsor Protocol Number: SALYCENDO | Start Date*: 2016-08-29 |
Sponsor Name:Radboudumc | ||
Full Title: The effects of acetylsalicylic acid on immunoparalysis following human endotoxemia. | ||
Medical condition: We will investigate the effects of acetylsalicylic acid on immunoparalysis following human endotoxemia in healthy male volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003296-60 | Sponsor Protocol Number: Oxidise | Start Date*: 2018-04-09 |
Sponsor Name:University Hospital Tuebingen | ||
Full Title: Empagliflozin effect on glucose toxicity in type 2 diabetes patients - a randomized, open-label, controlled, parallel group, exploratory study | ||
Medical condition: Patients with T2DM aged 40 to 70 years (including) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002222-12 | Sponsor Protocol Number: G1XCGD.02 | Start Date*: 2015-10-08 |
Sponsor Name:Genethon | ||
Full Title: A phase I/II, non-randomized, monocentric, open-label study of autologous CD34+ cells transduced with the G1XCGD lentiviral vector in patients with X-Linked Chronic Granulomatous Disease. | ||
Medical condition: Chronic Granulomatous Disease (CGD) is a rare inherited disorder (1/250,000) of the phagocytes characterized by the inability of phagocytes (monocytes and neutrophils) to produce reactive oxygen sp... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000887-27 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-05-23 | |||||||||||||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||||||||||||
Full Title: Pilot Trial: The effects of intravenous heme arginate on HO-1 expression and oxidative stress in the human heart | |||||||||||||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000942-39 | Sponsor Protocol Number: NL34476.068.11 | Start Date*: 2011-06-20 | ||||||||||||||||
Sponsor Name:CTMM, the Center for Translational Molecular Medicine | ||||||||||||||||||
Full Title: Effects of thyroid hormone treatment on mitochondrial function, ectopic fat accumulation, insulin sensitivity and brown adipose tissue in type 2 diabetes mellitus. | ||||||||||||||||||
Medical condition: This trial includes overweight patients with both hypothyroidism and type 2 diabetes. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001342-19 | Sponsor Protocol Number: YHGT-CEV-R1 | Start Date*: 2020-11-13 | |||||||||||
Sponsor Name:Asieris MediTech Co., Ltd. | |||||||||||||
Full Title: A double blind, prospective, randomized, placebo controlled, multi-center phase 3 study to evaluate efficacy and safety of Cevira® in patients with cervical histologic high-grade squamous intraepit... | |||||||||||||
Medical condition: Patients with cervical histologic HSIL. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) SK (Completed) PL (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015600-26 | Sponsor Protocol Number: CSPP100ADE05T | Start Date*: 2009-12-07 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Würzburg | ||||||||||||||||||
Full Title: An open label prospective pilot-study to determine the improvement of impaired endothelial function and endothelial progenitor cell numbers following treatment with Aliskiren 300 mg in patients wit... | ||||||||||||||||||
Medical condition: Determination of the improvement of impaired endothelial function and endothelial progenitor cell numbers following treatment with Aliskiren 300 mg in patients with coronary artery disease and hype... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000764-30 | Sponsor Protocol Number: HOT-LOCO | Start Date*: 2021-07-06 | |||||||||||||||||||||
Sponsor Name:Karolinska University Hospital | |||||||||||||||||||||||
Full Title: Hyperbaric Oxygen for Treatment of Long COVID syndrome; A Randomized, Placebo-Controlled, Double-Blind, Phase II Clinical Trial | |||||||||||||||||||||||
Medical condition: Long COVID, post-acute COVID-19 Syndrome, post COVID-19 Syndrome (ICD-10 U09.0) | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001725-26 | Sponsor Protocol Number: X-CGD-Version2 | Start Date*: 2013-03-12 | |||||||||||
Sponsor Name:Johann Wolfgang Goethe-University | |||||||||||||
Full Title: A Phase I/II Gene Therapy trial for X-CGD with a SIN gamma retroviral vector | |||||||||||||
Medical condition: Chronic granulomatous disease (CGD) is a congenital immunodeficiency, in which neutrophil granulocytes and monocytes are not capable of producing reactive oxygen species and therefore are unable to... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003299-15 | Sponsor Protocol Number: METFORAGING | Start Date*: 2021-10-19 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital La Paz | ||
Full Title: A double blinded, phase II, placebo controlled, single center randomized clinical trial to evaluate metformin compared with placebo for reversal of accelerated biological aging in persons living wi... | ||
Medical condition: Patients with HIV and accelerated biological aging | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004708-20 | Sponsor Protocol Number: RIFSYS | Start Date*: 2014-03-27 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: A placebo controlled single centre double blind randomised trial to investigate the efficacy of rifaximin versus placebo in improving systemic inflammation and neutrophil malfunction in patients wi... | ||||||||||||||||||
Medical condition: Cirrhosis and chronic hepatic encephalopathy | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001640-56 | Sponsor Protocol Number: PI12/01866 | Start Date*: 2014-01-31 | |||||||||||
Sponsor Name:Fundación Para la Investigación Biomédica de Córdoba | |||||||||||||
Full Title: Crossover clinical trial, randomized, double blind, placebo controlled trial. Modulation of cellular mediators and repair endothelial damage in patients with chronic renal disease through inhibitio... | |||||||||||||
Medical condition: Patients with chronic kidney disease and asymptomatic hyperuricemia on the balance of mechanisms of vascular injury and repair. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003270-14 | Sponsor Protocol Number: POSA-FLU | Start Date*: 2017-11-06 |
Sponsor Name:UZ Leuven | ||
Full Title: A phase IV, interventional, non-blinded, randomized, controlled, multicenter study of Posaconazole prophylaxis for the prevention of influenza-associated aspergillosis (IAA) in critically ill patients | ||
Medical condition: invasive aspergillosis in critically ill patients with influenza pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) NL (Completed) FR (Completed) | ||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
