- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Peroxidase.
Displaying page 1 of 1.
| EudraCT Number: 2021-006220-40 | Sponsor Protocol Number: 2022-0101-01 | Start Date*: 2022-06-30 | ||||||||||||||||||||||||||
| Sponsor Name:Hvidovre Hospital, Department of Gynecology | ||||||||||||||||||||||||||||
| Full Title: Double-blinded randomized placebo-controlled trial on tacrolimus in women with an euploid pregnancy loss and PCOS and/or thyroid autoimmunity | ||||||||||||||||||||||||||||
| Medical condition: Polycystic ovarian syndrome and/or thyroid autoimmunity in combination with an euploid pregnancy loss | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2005-004684-31 | Sponsor Protocol Number: 2809SELENIUM | Start Date*: 2006-04-20 |
| Sponsor Name:Barts and the London NHS Trust | ||
| Full Title: Does Selenium Supplementation reduce Oxidative Stress associated with Subarachnoid Haemorrhage? | ||
| Medical condition: Patients with spontaneous subarachnoid haemorrhage (non-traumatic) admitted to the Intensive Vare Unit of the Royal London Hospital. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003571-12 | Sponsor Protocol Number: GLU0409 | Start Date*: 2006-11-15 |
| Sponsor Name:Barts and the London NHS Trust | ||
| Full Title: Breath Methionine and Other Indices of Oxidant Stress in the Critical Care Setting. The effect of two doses of Dipeptiven given independently of parenteral nutrition. | ||
| Medical condition: 60 consecutive critically ill patients will be recruited with illnesses such as severe infection, trauma and post-surgery. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000719-19 | Sponsor Protocol Number: 09/100/10 | Start Date*: 2011-05-05 |
| Sponsor Name:University of Birmingham | ||
| Full Title: A Randomised Controlled Trial of the Efficacy and Mechanism of Levothyroxine Treatment on Pregnancy and Neonatal Outcomes in Women with Thyroid Antibodies. (TABLET: Thyroid AntiBodies and LEvoThyro... | ||
| Medical condition: Thyroid autoimmunity and history of miscarriage or infertility. | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002436-82 | Sponsor Protocol Number: EC11-441 | Start Date*: 2012-12-13 |
| Sponsor Name:Isabel Pinilla Lozano | ||
| Full Title: Melatonin effects on visual and sleep patterns anomalies in subjects diagnosed with Retinitis Pigmentosa | ||
| Medical condition: To evaluate the sleep quality in patients with Retinitis Pigmentosa | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006782-83 | Sponsor Protocol Number: EC08/00230 | Start Date*: 2013-09-24 |
| Sponsor Name:Hospital Universitario Virgen de las Nieves | ||
| Full Title: Prevention MODS by modulating the inflammatory response through melatonin administration in surgical patients with severe sepsis. | ||
| Medical condition: Septic patients of abdominal surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-001074-26 | Sponsor Protocol Number: S-CPR2011 | Start Date*: 2011-11-17 | |||||||||||
| Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin | |||||||||||||
| Full Title: Effect of High Dose Selenium on Inflammation and Neurological Outcome after Cardiac Arrest: A randomized, double blind placebo controlled phase 2a study | |||||||||||||
| Medical condition: Cardiac Arrest with successful resuscitation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001820-39 | Sponsor Protocol Number: 1984 | Start Date*: 2012-12-14 |
| Sponsor Name:Academic medical centre | ||
| Full Title: Levothyroxine for euthyroid women with recurrent miscarriage and thyroid autoimmunity : a randomized controlled trial | ||
| Medical condition: Thyroid autoimmunity is associated with recurrent miscarriage and preterm birth. Thyroid autoimmunity means there is a normal thyroid function, but presence of thyroid antibodies, thyroid peroxidas... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001088-11 | Sponsor Protocol Number: s56489 | Start Date*: 2014-07-29 |
| Sponsor Name:MEDA | ||
| Full Title: Academic study on the effects of MP 29-02 nasal spray on inflammatory mediators in allergic rhinitis | ||
| Medical condition: Allergic rhinitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004085-17 | Sponsor Protocol Number: 19IC5548 | Start Date*: 2020-03-18 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Treating severe paediatric asthma; a randomised controlled trial of mepolizumab and omalizumab (TREAT trial) | |||||||||||||
| Medical condition: Asthma | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001125-26 | Sponsor Protocol Number: ORG322 | Start Date*: 2006-08-04 |
| Sponsor Name:University of Aberdeen | ||
| Full Title: A randomised controlled trial of oral l-arginine supplementation on platelet and endothelial function and walking distance in patients with peripheral arterial disease | ||
| Medical condition: Peripheral arterial disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001107-38 | Sponsor Protocol Number: SESCHI.26371 | Start Date*: 2008-05-26 | |||||||||||
| Sponsor Name:Cefak KG | |||||||||||||
| Full Title: Dose finding study to investigate efficacy and tolerability of a 6 month oral treatment with selenium in patients with autoimmune thyroiditis: prospective, controlled parallel group study with Cef... | |||||||||||||
| Medical condition: Autoimmune thyroiditis (Hashimoto-thyroiditis) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017825-21 | Sponsor Protocol Number: EC09/081 | Start Date*: 2012-11-19 | |||||||||||
| Sponsor Name:INSTITUTO ARAGONÉS DE CIENCIAS DE LA SALUD | |||||||||||||
| Full Title: Prospective, randomised, double-blind study to evaluate the efficacy of treatment with melatonin in adult patients with severe sepsis or septic shock. | |||||||||||||
| Medical condition: Severe sepsis or septic shock. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002964-15 | Sponsor Protocol Number: STH19102 | Start Date*: 2016-12-06 | |||||||||||
| Sponsor Name:Sheffield Teaching Hospitals | |||||||||||||
| Full Title: The Effect of Selenium Supplementation on Musculoskeletal Health in Older Women Double-blind, randomised, placebo-controlled trial | |||||||||||||
| Medical condition: Osteoporosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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