- Trials with a EudraCT protocol (71)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
71 result(s) found for: Glucose intolerance.
Displaying page 1 of 4.
EudraCT Number: 2006-005772-41 | Sponsor Protocol Number: LIMIT phase 2 version 1.0 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:investigator-driven research: Erasmus MC, Neurovascular Section | |||||||||||||
Full Title: LIMIT: Lowering the Incidence of vascular complications with Metformin in patients with Impaired glucose tolerance and a recent TIA or minor ischemic stroke: a phase 2, randomized, controlled trial | |||||||||||||
Medical condition: Patients with impaired glucose tolerance and a recent TIA or minor ischemic stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003426-28 | Sponsor Protocol Number: CBXIGT | Start Date*: 2007-08-10 | ||||||||||||||||
Sponsor Name:University Hospitals Birmingham NHS Trust | ||||||||||||||||||
Full Title: Cortisol metabolism and impaired glucose tolerance | ||||||||||||||||||
Medical condition: Impared glucose tolerance | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003483-59 | Sponsor Protocol Number: CVAL489A2429 | Start Date*: 2006-12-18 | |||||||||||
Sponsor Name:VU University Medical Centre | |||||||||||||
Full Title: PRESERVE TRIAL: Pancreatic beta-cell dysfunction REStorEd by Rosiglitazone and Valsartan Effects; A 52-week randomized controlled factorial study in subjects with impaired fasting glucose and/or im... | |||||||||||||
Medical condition: subjects with impaired fasting glucose (IFG; blood glucose > or = 5.6 and < 7 mmol/l) and/or impaired glucose tolerance (IGT; 2-h post-load glucose 7.8-11.1 mmol/l). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000899-40 | Sponsor Protocol Number: Guid/05/Met-GDM/001 | Start Date*: 2006-08-28 | |||||||||||
Sponsor Name:GUIDOTTI | |||||||||||||
Full Title: ASSESSMENT OF EFFECTS OF A 12-MONTH TREATMENT WITH METFORMIN ON INSULIN ACTION AND SECRETION IN WOMEN WITH PRIOR GESTATIONAL DIABETES MELLITUS (GDM) | |||||||||||||
Medical condition: previous gestational diabetes (GDM) and altered glucose metabolism in the post-partum period (Impaired Fasting Glucose or Impaired Gluocse Tolerance) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005980-26 | Sponsor Protocol Number: MAAS | Start Date*: 2012-07-04 | ||||||||||||||||||||||||||
Sponsor Name: | ||||||||||||||||||||||||||||
Full Title: Metformin and sitagliptin in patients with impaired glucose tolerance and a recent TIA or minor ischemic stroke - a multicenter, randomized, open-label phase II trial | ||||||||||||||||||||||||||||
Medical condition: Stroke Transient ischemic attack Impaired glucose tolerance | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024487-18 | Sponsor Protocol Number: DvitamininDM2_v1 | Start Date*: 2011-06-20 | ||||||||||||||||||||||||||
Sponsor Name:Dept. of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital | ||||||||||||||||||||||||||||
Full Title: Effects of vitamin D on beta cell function and insulin sensitivity in pre-diabetes and diabetes mellitus type 2 - EVIDENS | ||||||||||||||||||||||||||||
Medical condition: Impaired glucose tolerance, impaired fasting glucose and type 2 diabetes mellitus. Vitamin D deficiency. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2023-000033-33 | Sponsor Protocol Number: 83631 | Start Date*: 2023-05-03 | |||||||||||||||||||||
Sponsor Name:Maastricht University | |||||||||||||||||||||||
Full Title: Short-term safety and efficacy of ketohexokinase inhibition in patients with hereditary fructose intolerance. | |||||||||||||||||||||||
Medical condition: Hereditary fructose intolerance | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018708-99 | Sponsor Protocol Number: 1245.39 | Start Date*: 2010-10-19 | ||||||||||||||||
Sponsor Name:BOEHRINGER ING. | ||||||||||||||||||
Full Title: An open-label, phase IIb study to determine acute (after the first dose administration) and chronic (after 28 days of treatment) effects of the sodium-glucose co-transporter-2 (SGLT-2) inhibitor ... | ||||||||||||||||||
Medical condition: patients with IGT or type 2 diabetes mellitus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) DE (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004065-13 | Sponsor Protocol Number: Metform02 | Start Date*: 2013-11-27 | |||||||||||
Sponsor Name:Central Manchester University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Metformin treatment vs a diabetes model of antenatal care in women with mild fasting hyperglycaemia diagnosed in pregnancy: a pilot study | |||||||||||||
Medical condition: Gestational diabetes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001733-86 | Sponsor Protocol Number: 1710 | Start Date*: 2014-10-15 |
Sponsor Name:Maastricht University | ||
Full Title: The effect of L-arginine on brown adipose tissue metabolism in South Asian and white Caucasian subjects | ||
Medical condition: Obesity, glucose intolerance, endothelial dysfunction | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002425-34 | Sponsor Protocol Number: T160/2018 | Start Date*: 2019-09-06 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: LIRAGLUTIDE IN THE PREVENTION OF T2DM AFTER GESTATIONAL DIABETES | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004386-24 | Sponsor Protocol Number: PEGACRO | Start Date*: 2015-12-04 | |||||||||||
Sponsor Name:DIPARTIMENTO DI MEDICINA CLINICA E CHIRURGIA - UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: Effect of GH receptor antagonist on insulin resistance associated with acromegaly | |||||||||||||
Medical condition: acromegaly | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002579-17 | Sponsor Protocol Number: WR 01102004 | Start Date*: 2006-11-08 |
Sponsor Name:Medizinische Klinik B, Herzzentrum Ludwigshafen | ||
Full Title: A double-blind, randomised placebo controlled study of the effects of Acarbose on endothelial function, hemostatic and fibrinolytic plasmatic factors in patients with stable coronary artery disease... | ||
Medical condition: 1. To study the effect of Acarbose treatment on endothelial function as a potential mechanism for the beneficial effects of better postprandial glycemic control in patients with impaired glucose to... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000872-41 | Sponsor Protocol Number: BGP-15-CLIN-IR01 | Start Date*: 2005-04-19 |
Sponsor Name:N-Gene Research & Development Ltd. | ||
Full Title: RANDOMIZED DOUBLE-BLIND, MULTIPLE DOSE, PLACEBO-CONTROLLED STUDY TO DETERMINE THE INSULIN SENSITIZING EFFECT OF BGP-15 IN PATIENTS WITH INSULIN RESISTANCE | ||
Medical condition: The metabolic syndrome is characterized by central obesity, atherogenic dyslipidemia, insulin resistance or glucose intolerance; prothrombotic state; raised blood pressure, proinflammatory state | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004706-25 | Sponsor Protocol Number: V1290413 | Start Date*: 2014-04-02 |
Sponsor Name:University of Edinburgh (ACCORD) [...] | ||
Full Title: A Feasibility study looking at the use of Glibenclamide and metfoRmin versus stAndard Care in gEstational diabeteS | ||
Medical condition: Gestational Diabetes Mellitus (GDM) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004679-36 | Sponsor Protocol Number: 05 2015-001 | Start Date*: 2006-12-13 | |||||||||||
Sponsor Name:Laboratoire HRA Pharma | |||||||||||||
Full Title: Prospective, open-label, multicenter, international study of mifepristone for symptomatic treatment of Cushing's syndrome caused by ectopic Adrenal Corticotrophin Hormone (ACTH) secretion. | |||||||||||||
Medical condition: Treatment of Cushing's syndrome caused by ectopic Adrenal Corticotrophin Hormone (ACTH) secretion. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004875-61 | Sponsor Protocol Number: 15778303 | Start Date*: 2016-02-05 |
Sponsor Name:CHU TOULOUSE | ||
Full Title: Influence of apelin on insulin sensitivity in type 2 diabetic volunteers | ||
Medical condition: type 2 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001244-38 | Sponsor Protocol Number: 14SM1971 | Start Date*: 2014-07-16 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Preventing Recurrent Gestational Diabetes Mellitus with Early Metformin Intervention | |||||||||||||
Medical condition: Gestational diabetes mellitus. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001390-88 | Sponsor Protocol Number: NT13034 | Start Date*: 2012-06-05 |
Sponsor Name:Institute for Clinical and Experimental Medicine | ||
Full Title: Cardioprotective and metabolic effects of metformin in patients with heart failure and diabetes | ||
Medical condition: type 2 diabetes mellitus, heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002240-24 | Sponsor Protocol Number: SIMASPK01b | Start Date*: 2019-06-27 |
Sponsor Name:Institut klinické a experimentální medicíny | ||
Full Title: The evolution of advanced microangiopathic diabetic complications before and after simultaneous pancreas and kidney transplantation evaluated with progressive non-invasive methods | ||
Medical condition: Surgical complications (hernia) after simultaneous pancreas and kidney transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Trial now transitioned) | ||
Trial results: (No results available) |
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