- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1,035)
34 result(s) found for: EME.
Displaying page 1 of 2.
| EudraCT Number: 2009-017134-47 | Sponsor Protocol Number: EMPOWaR | Start Date*: 2010-03-04 | ||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
| Full Title: Efficacy of Metformin in Pregnant Obese Women, a Randomised Controlled Trial. | ||||||||||||||||||
| Medical condition: Obesity in pregnancy | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000563-81 | Sponsor Protocol Number: EME | Start Date*: 2014-07-29 | |||||||||||
| Sponsor Name:FUNDACION PUBLICA ANDALUZA PARA LA GESTION DE LA INVESTIGACION EN SALUD DE SEVILLA | |||||||||||||
| Full Title: Metformin treatment of minimal hepatic encephalopathy in patients with liver cirrhosis | |||||||||||||
| Medical condition: minimal hepatic encephalopathy in patients with liver cirrhosis | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005721-43 | Sponsor Protocol Number: D4280C00002 | Start Date*: 2012-05-14 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Phase III, Randomized, Multicenter, Double-Blind, Double Dummy, Parallel Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime-Avibactam (CAZ-AVI, formerly C... | ||
| Medical condition: Complicated Urinary Tract Infections (cUTIs) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GR (Completed) BE (Completed) BG (Completed) DE (Completed) CZ (Completed) SK (Completed) PT (Completed) HU (Completed) | ||
| Trial results: View results | ||
| 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 | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005722-21 | Sponsor Protocol Number: D4280C00004 | Start Date*: 2012-06-05 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Phase III, Randomized, Multicenter, Double-Blind, Double Dummy, Parallel Group, Comparative Study to Determine the Efficacy, Safety, and Tolerability of Ceftazidime-Avibactam (CAZ-AVI, formerly C... | ||
| Medical condition: Complicated Urinary Tract Infections (cUTIs) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GR (Completed) DE (Completed) CZ (Completed) ES (Completed) IT (Completed) BG (Completed) PL (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-005342-63 | Sponsor Protocol Number: UoL001206 | Start Date*: 2016-06-23 |
| Sponsor Name:University of Liverpool | ||
| Full Title: Mindex: The efficacy and safety of very low dose dexamethasone used to facilitate the extubation of ventilator dependent preterm babies who are at high risk of bronchopulmonary dysplasia | ||
| Medical condition: Bronchopulmonary dysplasia | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000935-18 | Sponsor Protocol Number: UoL000841 | Start Date*: 2012-06-28 | |||||||||||
| Sponsor Name:University of Liverpool [...] | |||||||||||||
| Full Title: TAILoR – (TelmisArtan and InsuLin Resistance in HIV): A Dose-Ranging Phase II Randomised Open-Labelled Trial of Telmisartan as a strategy for the Reduction of Insulin Resistance in HIV-Positive Ind... | |||||||||||||
| Medical condition: Insulin resistance in HIV-positive patients treated with antiretroviral therapy | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004478-41 | Sponsor Protocol Number: LCC001 | Start Date*: 2015-03-10 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Phase III trial in IntrahepaTic CHolestasis of pregnancy (ICP) to Evaluate urSodeoxycholic acid (UDCA) in improving perinatal outcomes | |||||||||||||
| Medical condition: Intrahepatic Cholestasis of pregnancy | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004557-14 | Sponsor Protocol Number: NA | Start Date*: 2015-02-09 | |||||||||||
| Sponsor Name:King's College London [...] | |||||||||||||
| Full Title: Prospective randomised marker-based trial to assess the clinical utility and safety of biomarker-guided immunosuppression withdrawal in liver transplantation | |||||||||||||
| Medical condition: Immunosuppression withdrawal in liver transplantation | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-004271-78 | Sponsor Protocol Number: CIAOII | Start Date*: 2016-05-31 | |||||||||||
| Sponsor Name:King's College London | |||||||||||||
| Full Title: Randomised controlled trial of the short term effects of OROS-methylphenidate on ADHD symptoms and behavioural outcomes in young male prisoners with attention deficit hyperactivity disorder | |||||||||||||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001010-17 | Sponsor Protocol Number: 16SM3217 | Start Date*: 2016-08-26 | ||||||||||||||||
| Sponsor Name:Imperial College, London | ||||||||||||||||||
| Full Title: Nucleos(t)ide withdrawal in HBeAg negative hepatitis B virus infection to promote HBsAg clearance. (NUC-B) | ||||||||||||||||||
| Medical condition: Hepatitis B viral infection | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-000585-38 | Sponsor Protocol Number: SQ411218 | Start Date*: 2019-08-20 |
| Sponsor Name:University Hospitals Coventry and Warwickshire NHS Trust | ||
| Full Title: Chronic Endometritis and Recurrent Miscarriage - The CERM trial | ||
| Medical condition: Chronic Endometritis and Recurrent Miscarriage | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015852-11 | Sponsor Protocol Number: TC-FMISO-PET-06-1413 | Start Date*: 2012-02-03 |
| Sponsor Name:Hospital Universitario Dr. Negrin | ||
| Full Title: 18F-FMISO-PET in High Grade Gliomas: Assessment of Tumor Hypoxia and Effect of Spinal Cord Stimulation | ||
| Medical condition: Hypoxia in malignant brain tumors: high grade gliomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000058-73 | Sponsor Protocol Number: LIPS | Start Date*: 2012-09-14 | |||||||||||
| Sponsor Name:University of Liverpool [...] | |||||||||||||
| Full Title: A multi-centre (UK) double-blind randomised parallel group placebo controlled trial to evaluate the efficacy, safety, and tolerability of Intravenous Immunoglobulin (IVIg) 0.5g/kg plus standard tre... | |||||||||||||
| Medical condition: Complex Regional Pain Syndrome | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003272-12 | Sponsor Protocol Number: SIVS1012 | Start Date*: 2014-04-08 |
| Sponsor Name:Moorfields Eye Hospital | ||
| Full Title: Clinical Efficacy and Mechanistic Evaluation of Aflibercept for Proliferative Diabetic Retinopathy | ||
| Medical condition: Proliferative Diabetic Retinopathy (PDR) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-005390-36 | Sponsor Protocol Number: UoL001109 | Start Date*: 2016-02-17 | |||||||||||
| Sponsor Name:The University of Liverpool | |||||||||||||
| Full Title: Optimal utilisation of biologic drugs in Behçet’s Disease: a randomised controlled trial of infliximab (IFX) verses alpha interferon (aIFN), with genotyping and metabolomic profiling, towards a str... | |||||||||||||
| Medical condition: Behcets Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001382-10 | Sponsor Protocol Number: CS/2015/4775 | Start Date*: 2019-01-21 | |||||||||||
| Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
| Full Title: Treatment of Barth Syndrome by CARDIOlipin MANipulation (CARDIOMAN): A randomised placebo controlled pilot trial conducted by the nationally commissioned Barth Syndrome Service | |||||||||||||
| Medical condition: Barth Syndrome is a rare, life threatening, genetic disease which affects young males. It is caused by abnormal fats (lipids) in the powerhouses of cells (mitochondria) and those who suffer with it... | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001389-10 | Sponsor Protocol Number: IASO | Start Date*: 2017-09-28 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust & University of Cambridge | |||||||||||||
| Full Title: A phase II randomised placebo controlled double blinded trial of Interleukin 1 blockade in Acute Severe Colitis | |||||||||||||
| Medical condition: Acute Severe Ulcerative Colitis | |||||||||||||
|
|||||||||||||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003600-23 | Sponsor Protocol Number: APRICOT | Start Date*: 2016-04-01 | |||||||||||
| Sponsor Name:Guy's and St Thomas NHS Foundation Trust | |||||||||||||
| Full Title: Treatment of Pustular Psoriasis with the IL-1 receptor antagonist anakinra: a randomised, placebo controlled trial and associated mechanistic studies | |||||||||||||
| Medical condition: Acral Pustular Psoriasis, specifically but not limited to Palmo-Plantar Pustulosis will be the target population for therapeutic intervention with Anakinra in this study. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000896-99 | Sponsor Protocol Number: AC16148 | Start Date*: 2017-06-20 | ||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
| Full Title: A multicentre prospective randomised open-label blinded end-point controlled trial of high-sensitivity cardiac troponin I-guided combination angiotensin receptor blockade and beta blocker therapy t... | ||||||||||||||||||
| Medical condition: Myocardial toxicity and the development of left ventricular systolic dysfunction | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| 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
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| 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. | |
Query did not match any studies.