- Trials with a EudraCT protocol (64)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
64 result(s) found for: Self-monitoring.
Displaying page 1 of 4.
EudraCT Number: 2004-002731-62 | Sponsor Protocol Number: HMR1964A/3514 | Start Date*: 2005-06-28 | |||||||||||
Sponsor Name:AVENTIS PHARMA S.P.A. | |||||||||||||
Full Title: OPTIMISATION OF INSULIN TREATMENT OF TYPE 2 DIABETES MELLITUS BY TELECARE ASSISTANCE FOR SELF MONITORING OF BLOOD GLUCOSE ELEONOR STUDY | |||||||||||||
Medical condition: TYPE 2 DIABETES MELLITUS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004640-35 | Sponsor Protocol Number: EFC11681 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: A 24-week, Randomized, Open-label, Parallel Group, Multicenter Comparison of Lantus® (Insulin Glargine) Given Once Daily Versus Neutral Protamine Hagedorn (NPH) Insulin in Children With Type 1 Diab... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002607-12 | Sponsor Protocol Number: JVSRS08 | Start Date*: 2008-08-08 |
Sponsor Name:Central Manchester& Manchester Children's University Hospitals NHS Trust | ||
Full Title: Sitagliptin vs sulphonylurea based treatments in Muslim patients with Type 2 diabetes during Ramadan | ||
Medical condition: Muslim patients with type 2 diabets fasting during Ramadan | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-003630-15 | Sponsor Protocol Number: HypoAna | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:Steno Diabetes Center | |||||||||||||
Full Title: The effect of insulin analogues and human insulin on the incidence of severe hypoglycae-mia in hypoglycaemia prone type 1 diabetic patients | |||||||||||||
Medical condition: Type 1 diabetes - E10.8 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005196-16 | Sponsor Protocol Number: H8O-MC-GWBQ | Start Date*: 2012-07-24 | |||||||||||
Sponsor Name:Amylin Pharmaceuticals, Inc. | |||||||||||||
Full Title: Safety and Efficacy of Exenatide as Monotherapy and Adjunctive Therapy to Oral Antidiabetic Agents in Adolescents with Type 2 Diabetes | |||||||||||||
Medical condition: Treatment of Type 2 diabetes mellitus | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010913-59 | Sponsor Protocol Number: LANTU_L_04079 | Start Date*: 2009-05-19 |
Sponsor Name:Sanofi-Aventis Deutschland GmbH | ||
Full Title: Health Assessment, Patient treatment satisfaction and Quality-of-Life in insulin-naive type 2 diabetes Patients uncontrolled on OHA treatment initiating basal insulin therapy with either insulin gl... | ||
Medical condition: Diabetes mellitus type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-006164-59 | Sponsor Protocol Number: H80-BP-GWBG | Start Date*: 2006-05-18 |
Sponsor Name:Eli Lilly and Company Limited | ||
Full Title: An Open Label Study Comparing Exenatide with Basal Insulin in Achieving an HbA1c of <_7.4% with Minimum Weight Gain, in Type 2 Diabetes Patients who are not Achieving Adequate HbA1c Control on Oral... | ||
Medical condition: Type 2 Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004078-40 | Sponsor Protocol Number: CQR14002 | Start Date*: 2015-01-28 | |||||||||||
Sponsor Name:CeQur Corp. | |||||||||||||
Full Title: A Prospective, Single Center, Observational Study to Assess the Performance, Safety, and Patient Reported Outcomes of Insulin Delivery with PaQ® in Patients with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004680-31 | Sponsor Protocol Number: 2018-004680-31 | Start Date*: 2019-08-16 | ||||||||||||||||
Sponsor Name:Lene Ringholm | ||||||||||||||||||
Full Title: A randomised controlled trial comparing the effect of the faster-acting insulin analog - insulin Fiasp® – versus insulin Novorapid® in the treatment of women with type 1 or type 2 diabetes during p... | ||||||||||||||||||
Medical condition: Type 1 and type 2 diabetes during pregnancy and lactation | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003986-25 | Sponsor Protocol Number: ADAMPA | Start Date*: 2017-05-05 | |||||||||||
Sponsor Name:Instituto de Investigación Sanitaria INCLIVA | |||||||||||||
Full Title: Impact of self-measurement of blood pressure and self-adjustment of antihypertensive medication in the control of hypertension and adherence to treatment. A pragmatic, randomized, controlled clinic... | |||||||||||||
Medical condition: Arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006273-25 | Sponsor Protocol Number: BC20728 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A multi-center, double-blind, randomized, placebo-controlled, titration study to investigate the safety, the tolerability and the pharmacodynamic profiles of different doses of RO5073031 in patient... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004864-29 | Sponsor Protocol Number: F3Z-EW-IOPJ | Start Date*: 2008-02-13 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Prospective Randomized Trial to Compare Basal Bolus therapies that use either Insulin Lispro Protamine Suspension or Insulin Glargine together with Lispro Insulin in Patients with Type 2 Diabetes | |||||||||||||
Medical condition: Type II diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GR (Completed) GB (Completed) BE (Completed) SK (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018437-21 | Sponsor Protocol Number: LANTU_C_03680 | Start Date*: 2010-06-07 | |||||||||||
Sponsor Name:SANOFI AVENTIS GROUPE | |||||||||||||
Full Title: A 24-week, multicenter, international, randomized (1:1), parallel-group, open-label, comparative study of insulin glargine versus liraglutide in insulin-naïve patients with Type 2 diabetes treated ... | |||||||||||||
Medical condition: Type 2 diabetes not adequately controlled | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) IE (Completed) ES (Completed) SE (Completed) AT (Completed) FI (Completed) FR (Completed) NL (Completed) GR (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003941-13 | Sponsor Protocol Number: I2R-MC-BIAK | Start Date*: 2013-03-28 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Comparison of LY2605541 versus Human Insulin NPH as Basal Insulin Treatment in Insulin-Naïve Patients with Type 2 Diabetes Mellitus not Adequately Controlled with 2 or more Oral Antihyperglycemic... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005378-58 | Sponsor Protocol Number: NN1998-2161 | Start Date*: 2006-07-12 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Insulina humana preprandial inhalada con el sistema AERx® iDMS frente a insulina aspart s.c. en diabetes tipo 2: ensayo de 52 semanas de duración, abierto, multicéntrico, aleatorizado seguido de ... | |||||||||||||
Medical condition: Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DK (Prematurely Ended) GB (Completed) DE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005101-36 | Sponsor Protocol Number: LPS14584 | Start Date*: 2016-05-06 | |||||||||||
Sponsor Name:sanofi-aventis Groupe | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Open-label, Parallel-group Study Comparing the Efficacy and Safety of Toujeo® and Tresiba® in Insulin-Naive Patients with Type 2 Diabetes Mellitus Not Adequately... | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) GR (Completed) HU (Completed) CZ (Completed) SK (Completed) FR (Completed) GB (Completed) SI (Completed) BG (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005385-39 | Sponsor Protocol Number: EFC10007 | Start Date*: 2007-06-14 | |||||||||||
Sponsor Name:sanofi-aventis recherche et developpement | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel-Group, Multicenter, Multinational Study to Assess Glycemic Control with Rimonabant in Comparison with Glimepiride over 1 Year in Overweight/Obese Type 2 Diabeti... | |||||||||||||
Medical condition: Overweight/Obese Type 2 Diabetic Patients Not Adequately Controlled with Metformin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SE (Prohibited by CA) FI (Completed) ES (Completed) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004733-15 | Sponsor Protocol Number: EX1729-1778 | Start Date*: 2007-02-26 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 12-months multi-national, multi-centre, double-blind, randomised, parallel safety and efficacy comparison of insulin detemir produced by the current process and insulin detemir produced by the NN... | |||||||||||||
Medical condition: Type I diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008974-30 | Sponsor Protocol Number: PHX1149-PROT302 | Start Date*: 2009-09-08 | |||||||||||
Sponsor Name:Phenomix Corporation | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate Safety and Efficacy of Dutogliptin/PHX1149T in Subjects With Type 2 Diabetes Mellitus on a Background Medicat... | |||||||||||||
Medical condition: Type II Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003060-59 | Sponsor Protocol Number: NN304-1761 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Novo Nordisk Limited | |||||||||||||
Full Title: A 32 week, national, single-centre, open-labelled, randomised, cross-over trial comparing energy expenditure with insulin detemir versus NPH insulin using a basal-bolus regimen with insulin aspart ... | |||||||||||||
Medical condition: Type 1 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
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