- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Short acting insulin.
Displaying page 1 of 2.
EudraCT Number: 2019-001281-14 | Sponsor Protocol Number: Protocol_NN-ExFiasp_V_5.3 | Start Date*: 2019-06-18 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: A trial investigating the effect on blood glucose after the injection of fast-acting insulin aspart (Fiasp®) in comparison to insulin aspart (NovoRapid®) around exercise in participants with type 1... | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020684-20 | Sponsor Protocol Number: CLAF237A23135 | Start Date*: 2010-09-29 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 24-week, multi-center, double-blind, randomized, placebo-controlled, parallel-group study to assess the efficacy and safety of vildagliptin 50mg bid as an add-on therapy to insulin, with or witho... | |||||||||||||
Medical condition: Type II Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) DE (Completed) GB (Completed) BE (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019237-10 | Sponsor Protocol Number: FARM8MR2J7 | Start Date*: 2010-10-28 | |||||||||||
Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
Full Title: Multicenter prospective randomized open with a blinded end point (PROBE) parallel-group study on treatment with biphasic insulin BIAsp70/30 and short-acting insulin or rapid-acting analogue plus gl... | |||||||||||||
Medical condition: DM1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000780-27 | Sponsor Protocol Number: SPRINK-01 | Start Date*: 2011-04-19 | |||||||||||
Sponsor Name:Medizinische Universität Graz | |||||||||||||
Full Title: A single-center, randomized, controlled, 2-period cross-over, open-labelled trial to evaluate the impact of different application volumes on pharmacokinetic and pharmacodynamic properties of insul... | |||||||||||||
Medical condition: Diabetes mellitus type I | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000955-25 | Sponsor Protocol Number: ClinDiab-08 | Start Date*: 2017-05-12 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: A single-centre, open-label, randomized controlled trial of efficacy, safety and usability of a basal insulin algorithm incorporated in the GlucoTab system compared to standard care for glycaemic m... | |||||||||||||
Medical condition: Diabetes mellitus type 2 | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002070-36 | Sponsor Protocol Number: GLU-005 | Start Date*: 2004-12-22 | |||||||||||
Sponsor Name:Metcon Medicin AB | |||||||||||||
Full Title: Efficacy of MM005-Granulae as prophylaxis for nocturnal hypoglycemia in insulin treated Type 1 diabetic subjects. A double-blind, randomized, placebo-controlled phase II multi-center study in three... | |||||||||||||
Medical condition: Diabetes type I | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001089-10 | Sponsor Protocol Number: CV181-057 | Start Date*: 2008-12-02 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Phase 3b Trial to Evaluate the Efficacy and Safety of Saxagliptin Added to Insulin Monotherapy or to Insulin in Combination with Metformin in Subjects with ... | |||||||||||||
Medical condition: DIABETES, NOS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) HU (Completed) PL (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003733-34 | Sponsor Protocol Number: APIDR_L_05719 | Start Date*: 2011-09-13 | |||||||||||
Sponsor Name:ikfe – Institute for Clinical Research and Development | |||||||||||||
Full Title: Human Insulin Analogs: Evaluation of inflammatory mRNA expression of Macrophages and Endothelial function of Short-acting insulin – HERMES Pilot Study | |||||||||||||
Medical condition: Patients with Diabetes mellitus Type 2 and a stable basal supported oral therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006118-15 | Sponsor Protocol Number: CLAF237ADE07 | Start Date*: 2012-06-13 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Multicentric cross-over trial to assess the glycemic profiles on 8 weeks of vildagliptin and sitagliptin treatment, each, in type-2 diabetic patients with a pre-existing cardiovascular disease pre-... | |||||||||||||
Medical condition: type-2 diabetes mellitus with pre-existing cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003579-38 | Sponsor Protocol Number: APIDR_C_02083 | Start Date*: 2007-11-13 | |||||||||||
Sponsor Name:sanofi-aventis groupe | |||||||||||||
Full Title: Effect of insulin glulisine compared to insulin aspart and insulin lispro when administered by Continuous Subcutaneous Insulin Infusion (CSII) on specific pump parameters in patient with Type 1 Dia... | |||||||||||||
Medical condition: Type I Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) NL (Completed) AT (Completed) HU (Completed) IT (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013264-39 | Sponsor Protocol Number: VIAject-31J | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BIODEL inc. | |||||||||||||
Full Title: A Single-Center, Double Blind, Randomized Crossover Study Evaluating Injection Site Toleration of VIAject® 7, VIAject® 25 and Insulin Lispro in Subjects with Type 1 or Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Type 1 or Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000863-98 | Sponsor Protocol Number: GlucoTab@MobileCare | Start Date*: 2018-06-25 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: A single-centre, open-label, non-controlled trial of acceptance, usability, safety and efficacy of a tablet based workflow and decision support system with incorporated basal-insulin algorithm for ... | |||||||||||||
Medical condition: Diabetes mellitus type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001365-92 | Sponsor Protocol Number: 1 | Start Date*: 2016-10-10 | |||||||||||
Sponsor Name:Center for Diabetes Research, Gentofte Hospital | |||||||||||||
Full Title: Meal-time Administration of exenatide for Glycaemic control in type 1 diabetic Cases: A randomised, placebo-controlled trial | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005886-36 | Sponsor Protocol Number: EFC6016 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:Sanofi -Aventis Recherche & De'veloppement | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, 2-arm parallel-group, multicenter study with a 24-week main treatment period and an extension assessing the efficacy and safety of AVE0010 in patient... | |||||||||||||
Medical condition: Type II Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007769-21 | Sponsor Protocol Number: H9D-SB-ITAE | Start Date*: 2009-09-11 | |||||||||||
Sponsor Name:Lilly Deutschland GmbH | |||||||||||||
Full Title: A Randomized, Open-label Study on the Effects of Insulin Pen Devices on Glycemic Control in Children, Adolescents and Adults with Type 1 Diabetes: Novel Pen with Memory Function (HumaPen® Memoir) v... | |||||||||||||
Medical condition: Pts with type 1 diabetes mellitus based on the WHO criteria, at least 8 years old, used an insulin pen device to inject at least 4 insulin doses/day for at least 2 months prior to the study and cur... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000514-38 | Sponsor Protocol Number: NN304-1613 | Start Date*: 2004-11-22 | |||||||||||
Sponsor Name:Novo Nordisk Pharmaceuticals Ltd | |||||||||||||
Full Title: 4T study Treating to Target in Type 2 Diabetes A 36-month, Multi-centre, Open-label, Randomised, Parallel-group Trial Comparing the Safety, Efficacy and Durability of Adding a Basal Insulin versus ... | |||||||||||||
Medical condition: Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001461-18 | Sponsor Protocol Number: NN304-1632 | Start Date*: 2004-12-06 | |||||||||||
Sponsor Name:NOVO NORDISK | |||||||||||||
Full Title: A 20 week multi-national, open-labelled, randomised, three-group parallel trial comparing administration of insulin detemir morning, insulin detemir evening and NPH insulin evening as add-on to ora... | |||||||||||||
Medical condition: Combined therapy in diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003085-17 | Sponsor Protocol Number: EC/2007/49/PGMS | Start Date*: 2007-12-13 | |||||||||||
Sponsor Name:University of Surrey | |||||||||||||
Full Title: The effect of insulin detemir on energy balance, postprandial nutrient handling, body fat distribution,and adipose tissue metabolism and gene expression in patients with type 2 diabetes. | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004222-22 | Sponsor Protocol Number: U1111-1235-6899 | Start Date*: 2020-02-13 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: Adjustment of insulin Degludec to Reduce post-Exercise (nocturnal) hypoglycaeMia in people with diabetes – the ADREM study | ||
Medical condition: type 1 diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004622-81 | Sponsor Protocol Number: NN1998-1616 | Start Date*: 2007-11-02 | |||||||||||||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||||||||||||
Full Title: Inhaled preprandial human insulin with the AERx® iDMS versus subcutaneous injected insulin aspart in subjects with diabetes and asthma: a 52-week, open-label, multinational, randomised, parallel tr... | |||||||||||||||||||||||
Medical condition: Type 1 diabetes Type 2 diabetes Asthma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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