- Trials with a EudraCT protocol (139)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
139 result(s) found for: CGM.
Displaying page 1 of 7.
EudraCT Number: 2022-000800-37 | Sponsor Protocol Number: 421496 | Start Date*: 2022-09-06 |
Sponsor Name:St. Olav's University Hospital | ||
Full Title: An open, controlled investigation of the effect of micro-doses of glucagon on the performance of continuous glucose monitoring in patients with diabetes mellitus type 1. | ||
Medical condition: Diabetes mellitus type 1 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001631-31 | Sponsor Protocol Number: DHCL2019 | Start Date*: 2019-07-10 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Dual-Hormone Closed-Loop Glucose Control in Type 1 Diabetes | |||||||||||||
Medical condition: Patients with type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003261-20 | Sponsor Protocol Number: DHCL2014 | Start Date*: 2014-11-20 | |||||||||||
Sponsor Name:Hvidovre University Hospital | |||||||||||||
Full Title: Dual-Hormone Closed-Loop Glucose Control in Type 1 Diabetes | |||||||||||||
Medical condition: Patients with type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004041-32 | Sponsor Protocol Number: 0701 | Start Date*: 2020-06-01 |
Sponsor Name:University of Leicester | ||
Full Title: The effect of Canagliflozin 300mg, in subjects without diabetes after bariatric surgery, on glucose homeostasis (The CONTROL Study): A proof-of-concept, randomised, open-label, two period crossover... | ||
Medical condition: Postprandial hypoglycaemia after bariatric surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2019-002068-29 | Sponsor Protocol Number: ANCA_CGM | Start Date*: 2019-10-24 |
Sponsor Name:Medizinische Universität Graz, Universitätsklinik für Innere Medizin, Klinische Abteilung für Nephrologie | ||
Full Title: Influence of once vs twice daily corticosteroid administration on glycemia assessed by continuous glucose monitoring in patients with ANCA vasculitis | ||
Medical condition: ANCA vasculitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005836-31 | Sponsor Protocol Number: DHCL2021 | Start Date*: 2021-04-07 | |||||||||||
Sponsor Name:Steno Diabetes Center Copenhagen | |||||||||||||
Full Title: Dual-Hormone Closed-Loop Glucose Control in Adolescents with Type 1 Diabetes | |||||||||||||
Medical condition: Patients with type 1 diabetes | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
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: 2019-004080-43 | Sponsor Protocol Number: LPS16664 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:sanofi-aventis Private Co. Ltd. | |||||||||||||
Full Title: Suliqua® (iGlarLixi) in Participants uncontrolled on basal insulin to Evaluate the change of time in target Range By using Continuous Glucose Monitoring | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003715-94 | Sponsor Protocol Number: IDEAL | Start Date*: 2020-12-17 |
Sponsor Name:Institute for Clinical and Experimental Medicine | ||
Full Title: INSULIN THERAPY DE-INTENSIFICATION WITH iGlarLixi | ||
Medical condition: Type 2 diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001188-58 | Sponsor Protocol Number: IDIT001 | Start Date*: 2022-02-16 |
Sponsor Name:Göteborgs Universitet | ||
Full Title: The effect of anti-IL17 in new-onset type 1 diabetes: a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Type 1 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004674-97 | Sponsor Protocol Number: MB102-229 | Start Date*: 2015-01-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-controlled, Parallel Group, Phase 3 Study to Evaluate the Efficacy and Safety of Dapagliflozin as an Add-on to Insulin Therapy in Subjects with Type... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) FI (Completed) IT (Completed) DE (Completed) AT (Completed) ES (Completed) HU (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001485-35 | Sponsor Protocol Number: LPS17007 | Start Date*: 2022-10-03 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Open-Label, Parallel-Group Trial Comparing the Efficacy and Safety of Insulin Glargine 300 U/mL (Gla-300) and Insulin Degludec 100 U/mL (IDeg-100) in Insulin-Naï... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus and Renal Impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002817-78 | Sponsor Protocol Number: D5670C00007-Amendment1 | Start Date*: 2017-12-06 | |||||||||||
Sponsor Name:MedImmune Limited, a wholly owned subsidiary of AstraZeneca | |||||||||||||
Full Title: An Exploratory Phase 2a Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of MEDI0382 versus Placebo in Overweight/Obese Subjects with Type 2 Diabetes Mellitus ... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003761-28 | Sponsor Protocol Number: VP-00525 | Start Date*: 2015-12-22 |
Sponsor Name:Calibra Medical, Inc. | ||
Full Title: GLYCEMIC CONTROL AND TREATMENT SATISFACTION USING FINESSE VERSUS PEN FOR INITIATING BOLUS INSULIN DOSING IN TYPE 2 DIABETES MELLITUS PATIENTS NOT ACHIEVING GLYCEMIC TARGETS ON BASAL INSULIN WITH/WI... | ||
Medical condition: Type 2 Diabetes Mellitus (T2DM) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004186-83 | Sponsor Protocol Number: RZ358-606 | Start Date*: 2017-04-11 | ||||||||||||||||||||||||||
Sponsor Name:Rezolute, Inc. | ||||||||||||||||||||||||||||
Full Title: An Open-Label Multiple-Dose Study of RZ358 in Patients with Congenital Hyperinsulinism | ||||||||||||||||||||||||||||
Medical condition: Hypoglycemia associated with congenital hyperinsulinism | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) BG (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001702-33 | Sponsor Protocol Number: CV181-369 | Start Date*: 2016-01-07 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: A 24-week International, Multicenter, Randomized, Open-Label, Active-Controlled, Parallel Group, Phase 3b Trial with a 28-week Extension to Evaluate the Efficacy and Safety of Saxagliptin Co-admini... | |||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus and inadequate glycemic control on a stable dose of metformin | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) SE (Completed) DK (Completed) DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000157-87 | Sponsor Protocol Number: 2022-03 | Start Date*: 2022-08-23 |
Sponsor Name:Hvidovre Hospital | ||
Full Title: HypoBar I: Delaying intestinal glucose absorption to ameliorate post-bariatric hypoglycaemia. A randomized cross-over clinical trial. | ||
Medical condition: Post-bariatric hypoglycaemia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003318-35 | Sponsor Protocol Number: VX22-264-101 | Start Date*: 2023-09-25 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 1/2 Study to Evaluate the Safety, Tolerability, and Efficacy of VX-264 in Subjects With Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001915-22 | Sponsor Protocol Number: CKN-DASI-RYGB | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Center for Clinical Metabolic Research at Herlev-Gentofte Hospital | |||||||||||||
Full Title: Dasiglucagon in the treatment of postprandial hypoglycaemia after Roux-en-Y gastric bypass | |||||||||||||
Medical condition: Postprandial hyperinsulinemic hypoglycaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001941-42 | Sponsor Protocol Number: MDILiraglutid01/2012 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Västra Götalandsregionen (VGR) | |||||||||||||
Full Title: Addition of liraglutide to overweight patients with type 2 diabetes treated with multiple daily insulin injections (MDI) with inadequate glycaemic control | |||||||||||||
Medical condition: Diabetes Mellitus Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
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