- Trials with a EudraCT protocol (106)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
106 result(s) found for: Impaired Fasting Glucose.
Displaying page 1 of 6.
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: 2008-004497-40 | Sponsor Protocol Number: METIGT2008 | Start Date*: 2008-11-11 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: The effect of metformin on weight and cardiovascular risk markers in abdomenally obese subjects with impaired fasting glucose previously treated for 12 months with either rimonabant or placebo | |||||||||||||
Medical condition: Impaired fasting glucose | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2018-000823-15 | Sponsor Protocol Number: DIASA3 | Start Date*: 2019-10-18 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Glucose metabolism in South Asian women with impaired glucose tolerance or impaired fasting glucose. DIAbetes in South Asians – DIASA 3 A 12-week intervention trial with oral antidiabetic medicati... | |||||||||||||
Medical condition: Pre-diabetes in women of South Asian ethnicity. Women of South Asian ethnicity with previous gestational diabetes, where pre-diabetes in the form of impaired glucose tolerance or impaired fasting ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000940-28 | Sponsor Protocol Number: Final Protocol version 6 | Start Date*: 2007-11-28 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: The Rimonabant in treatment of Prediabetes Study: a randomised clinical trial of Rimonabant in the treatment of patients with Prediabetes | ||||||||||||||||||
Medical condition: Impaired Glucose tolerance and Impaired fasting Glycaemia (Together known as Prediabetes) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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: 2014-002766-73 | Sponsor Protocol Number: PHT/2014/44 | Start Date*: 2015-10-26 | ||||||||||||||||
Sponsor Name:Portsmouth Hospitals NHS Trust | ||||||||||||||||||
Full Title: The effect of oral Vitamin D supplementation on endothelial function, vascular inflammation, oxidative stress and insulin sensitivity in patients with impaired fasting glucose: A randomised, double... | ||||||||||||||||||
Medical condition: Impaired fasting glycaemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003532-39 | Sponsor Protocol Number: SitaBAT01 | Start Date*: 2014-11-24 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of sitagliptin on brown adipose tissue and whole-body metabolism in overweight pre-diabetic men | ||
Medical condition: Obesity, dyslipidemia and impaired glucose tolerance | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003803-30 | Sponsor Protocol Number: 2560/2008 | Start Date*: 2011-04-28 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | ||||||||||||||||||
Full Title: Effects of the treatment with metformin and/or sitagliptin on β- cell function and insulin resistance in women with prior gestational diabetes. | ||||||||||||||||||
Medical condition: previous gestational diabetes | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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: 2018-003283-31 | Sponsor Protocol Number: NL67170.068.18 | Start Date*: 2019-03-13 |
Sponsor Name:School of Nutrition and Translational research in Metabolism (NUTRIM), Maastricht University | ||
Full Title: MaasFlex: A Double-Blind, Randomized, Phase IV, Mechanistic, Placebo-Controlled, Cross-Over, Single-Center Study to Evaluate the Effects of 2 Weeks Dapagliflozin Treatment on Nocturnal Substrate Ox... | ||
Medical condition: Study to investigate the effect of dapagliflozin treatment on nocturnal substrate oxidation in overweight and obese subjects with a disrupted glucose homeostasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001711-30 | Sponsor Protocol Number: RIMON_R_00961 | Start Date*: 2006-10-11 | |||||||||||
Sponsor Name:sanofi aventis Groupe | |||||||||||||
Full Title: A Pan-European randomized, parallel group, two-arm placebo-controlled, double-blind multicenter study of Rimonabant 20mg once daily in the treatment of abdominally obese patients with impaired fast... | |||||||||||||
Medical condition: abdominally obese patients with impaired fasting blood glucose with or without other comorbidities | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) BE (Completed) PT (Prematurely Ended) CZ (Completed) SI (Completed) FR (Completed) NL (Prematurely Ended) NO (Completed) FI (Prematurely Ended) SE (Prematurely Ended) DK (Prematurely Ended) LT (Prematurely Ended) HU (Completed) SK (Completed) GR (Completed) AT (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002230-37 | Sponsor Protocol Number: CLAF237ANL05T | Start Date*: 2013-12-19 |
Sponsor Name:Erasmus Medical Center | ||
Full Title: “Novel Approach to Detect the Detailed Effects of Vildagliptin on Beta-cell Dynamics in Patients with Early-onset Type 2 Diabetes” | ||
Medical condition: impaired fasting glucose/impaired glucose tolerance, prediabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002997-31 | Sponsor Protocol Number: SCH/05/015 | Start Date*: 2006-08-10 |
Sponsor Name:Sheffield Children's NHS Trust | ||
Full Title: A multi-centre randomised trial of insulin detemir in pre-diabetes associated with cystic fibrosis. | ||
Medical condition: Individuals with cystic fibrosis develop diabetes. They exhibit abnormal glucose handling (impaired glucose tolerance), poor growth and a decline in lung function before overt diabetes develops. E... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003101-53 | Sponsor Protocol Number: ARTinMMS | Start Date*: 2007-01-10 | |||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||
Full Title: A randomised placebo controlled study of transdermal testosterone therapy (testosterone 1% hydroalcohol gel) to investigate the efficacy and safety in men with abdominal obesity, low testosterone l... | |||||||||||||
Medical condition: The metabolic syndrome constitutes a cluster of risk factors for cardiovascular disease with increased morbidity and mortality. The metabolic syndrome is referred to as a concomitant occurrence of ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001888-29 | Sponsor Protocol Number: 0816-2007 | Start Date*: 2007-11-19 |
Sponsor Name:University of Leipzig | ||
Full Title: Chronic inflammatory activation in fat tissue: an atherogenic factor in severe coronary artery disease. | ||
Medical condition: severe cardiovascular artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Prematurely Ended) | ||
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: 2009-016022-14 | Sponsor Protocol Number: PREVORAL 2 | Start Date*: 2009-09-29 | |||||||||||
Sponsor Name:UNIVERSITA` CAMPUS BIOMEDICO | |||||||||||||
Full Title: Studio aperto per la valutazione dell efficacia dell insulina spray buccale sul controllo glicometabolico in soggetti con ridotta tolleranza ai carboidrati (studio PREVORAL 2). | |||||||||||||
Medical condition: impaired glucose tolerance (IGT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000121-31 | Sponsor Protocol Number: PSYK-TREAT-HEALTHY | Start Date*: 2013-03-20 | |||||||||||
Sponsor Name:Prof., dr. med. Anders Fink-Jensen | |||||||||||||
Full Title: Does a GLP-1 receptor agonist change glucose tolerance in antipsychotic-treated patients? | |||||||||||||
Medical condition: Dysglycaemia, schizophrenia, paranoid psycosis, schizotypal disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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