- Trials with a EudraCT protocol (425)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
425 result(s) found for: Obesity.
Displaying page 3 of 22.
| EudraCT Number: 2009-013100-32 | Sponsor Protocol Number: pms.nov.001 | Start Date*: 2009-12-01 | |||||||||||
| Sponsor Name:University of Exeter [...] | |||||||||||||
| Full Title: Does modulating the gut hormones, incretins, modify vascular function, thereby reducing the risk of vascular complications in insulin resistant individuals? | |||||||||||||
| Medical condition: Obese (BMI equal or greater than 30) individuals at a high risk of diabetes, but without overt cardiovascular disease or taking oral hypoglycaemic, anti-hypetensive or lipid lowering therapies. Pur... | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017134-47 | Sponsor Protocol Number: EMPOWaR | Start Date*: 2010-03-04 | ||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
| Full Title: Efficacy of Metformin in Pregnant Obese Women, a Randomised Controlled Trial. | ||||||||||||||||||
| Medical condition: Obesity in pregnancy | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-003183-75 | Sponsor Protocol Number: 752/11 | Start Date*: 2012-01-23 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: the role of vitamin D supplementation in the prevention of cardiovascular risk factors | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000819-16 | Sponsor Protocol Number: VICSUB | Start Date*: 2006-03-14 | |||||||||||
| Sponsor Name:HYKS, sisätautien toimiala, diabetesklinikka | |||||||||||||
| Full Title: RIMONABANT-LÄÄKEHOIDON JA LAIHDUTUKSEN VAIKUTUKSET MAKSAN RASVAPITOISUUTEEN JA RASVAKUDOKSEN AINEENVAIHDUNTAAN METABOLISTA OIREYHTYMÄÄ SAIRASTAVILLA POTILAILLA | |||||||||||||
| Medical condition: Tutkimukseen osallistuu korkeintaan 20 VICTORIA-tutkimukseen jo osallistuvaa keskivartalolihavaa metabolista oireyhtymää sairastavaa potilasta | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004415-37 | Sponsor Protocol Number: NN8022-4179 | Start Date*: 2015-11-10 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Effect of liraglutide for weight management in paediatric subjects with Prader-Willi Syndrome. A randomised, placebo controlled, parallel group, multi-centre, multinational trial with a 16-week dou... | |||||||||||||
| Medical condition: Obesity (Prader-Willi syndrome) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) FR (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000693-26 | Sponsor Protocol Number: ATOHS | Start Date*: 2022-05-02 | |||||||||||
| Sponsor Name:ISTITUTO AUXOLOGICO ITALIANO | |||||||||||||
| Full Title: Crossover, Double-blind, Phase 2 Study of a Fixed Dose Combination of Atomoxetine and Acetazolamide Versus Placebo in Obesity Hypoventilation Syndrome | |||||||||||||
| Medical condition: Patients with obesity hypoventilation syndrome (OHS) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002479-37 | Sponsor Protocol Number: 1404-0036 | Start Date*: 2021-03-15 | |||||||||||
| Sponsor Name:Boehringer Ingelheim AB | |||||||||||||
| Full Title: A Phase II, randomized, double blind, parallel group,46 weeks dose-finding study of BI 456906 administered once weekly subcutaneously compared with placebo in patients with obesity or overweight | |||||||||||||
| Medical condition: obesity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) IE (Prematurely Ended) NL (Completed) BE (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000546-34 | Sponsor Protocol Number: NN8022-4392 | Start Date*: 2021-02-10 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Effect and safety of liraglutide 3.0 mg on weight management in children with obesity aged 6 to <12 years: 56-week, double-blind, randomised, placebo-controlled trial | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) PT (Trial now transitioned) NO (Not Authorised) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001715-30 | Sponsor Protocol Number: RIMON_R_00962 | Start Date*: 2006-10-23 | |||||||||||
| Sponsor Name:sanofi aventis Groupe | |||||||||||||
| Full Title: A 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 dyslipidemia with... | |||||||||||||
| Medical condition: abdominally obese patients with dyslipidemia with or without other comorbidities | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Prematurely Ended) CZ (Completed) SI (Completed) NL (Completed) SE (Prematurely Ended) FI (Prematurely Ended) DE (Prematurely Ended) SK (Completed) HU (Completed) GR (Completed) IT (Prematurely Ended) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002080-88 | Sponsor Protocol Number: NA | Start Date*: 2005-09-13 | |||||||||||
| Sponsor Name:Aintree Hospitals NHS Trust and University of Liverpool | |||||||||||||
| Full Title: A double−blind, placebo−controlled crossover trial to quantify the effects of sibutramine on energy intake and energy expenditure in obese subjects during a test meal | |||||||||||||
| Medical condition: Obesity defined as BMI > 30 kg /m2 | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005585-32 | Sponsor Protocol Number: 111111733104 | Start Date*: 2016-06-24 | |||||||||||
| Sponsor Name:Department of Biomedical Sciences, Faculty of Health Sciences, University of Copenhagen | |||||||||||||
| Full Title: Synergy effect of the appetite hormone GLP-1 (LiragluTide) and Exercise on maintenance of weight loss and health after a low calorie diet - the S-LiTE randomized trial | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004449-19 | Sponsor Protocol Number: CMBL949A12201 | Start Date*: 2022-04-11 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A randomized, placebo-controlled, participant-and investigator-blinded, sponsor open-label study to evaluate the safety, tolerability, and efficacy with different dosing regimens of subcutaneously ... | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002544-28 | Sponsor Protocol Number: 0364-011 | Start Date*: 2007-01-09 | |||||||||||
| Sponsor Name:Merck & Co. Inc. | |||||||||||||
| Full Title: A Phase IIb/III Randomized, Placebo-Controlled Clinical Trial to Study the Safety and Efficacy of MK-0364 in Overweight and Obese Patients With Type 2 Diabetes Mellitus (T2DM) | |||||||||||||
| Medical condition: Obesity in patients with type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) LT (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001540-38 | Sponsor Protocol Number: NN9536-4153 | Start Date*: 2015-08-24 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Investigation of safety and efficacy of once-daily semaglutide in obese subjects without diabetes mellitus. A 52-week, randomised, double-blind, placebo-controlled, nine-armed, parallel group, mul... | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001049-24 | Sponsor Protocol Number: NN8022-1839 | Start Date*: 2008-12-02 | ||||||||||||||||
| Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
| Full Title: Effect of liraglutide on body weight in non-diabetic obese subjects or overweight subjects with comorbidities A randomised, double-blind, placebo controlled, parallel group, multi-centre, multina... | ||||||||||||||||||
| Medical condition: Obesity and overweight Pre-diabetes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IE (Completed) FI (Completed) ES (Completed) DE (Completed) DK (Completed) AT (Completed) GB (Completed) FR (Completed) IT (Completed) NL (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-024414-61 | Sponsor Protocol Number: HJT-PEDOB-MET1 | Start Date*: 2011-12-21 | ||||||||||||||||
| Sponsor Name:Hospital de Girona Dr Josep Trueta | ||||||||||||||||||
| Full Title: Efectos endocrino-metabólicos, sobre la adiposidad visceral y parámetros de riesgo cardiovascular de la administración de metformina en niños prepuberales con obesidad y marcadores de riesgo para e... | ||||||||||||||||||
| Medical condition: Obesidad Infantil | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-001859-40 | Sponsor Protocol Number: 2019-041 | Start Date*: 2020-11-05 | |||||||||||||||||||||||||||||||
| Sponsor Name:Franciscus Gasthuis & Vlietland | |||||||||||||||||||||||||||||||||
| Full Title: PEROPERATIVE TRANEXAMIC ACID IN BARIATRIC FAST TRACK SURGERY TO REDUCE HEMORRAGE RATES | |||||||||||||||||||||||||||||||||
| Medical condition: Morbid obesity | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-005084-26 | Sponsor Protocol Number: A5351019 | Start Date*: 2007-01-18 | |||||||||||
| Sponsor Name:Pfizer Inc | |||||||||||||
| Full Title: A 2-YEAR, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE 3 STUDY TO EVALUATE THE LONG-TERM EFFICACY AND SAFETY OF CP-945,598 IN THE TREATMENT OF OBESE SUBJECTS | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) GB (Completed) FR (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002939-29 | Sponsor Protocol Number: NN9536-4734 | Start Date*: 2021-07-05 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Efficacy and safety of subcutaneous semaglutide 2.4 mg once-weekly in subjects with obesity and prediabetes | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DK (Completed) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000790-94 | Sponsor Protocol Number: NN9536-4999 | Start Date*: 2022-11-07 | |||||||||||
| Sponsor Name:Novo Nordisk A/S | |||||||||||||
| Full Title: Effect and safety of semaglutide 7.2 mg once-weekly in participants with obesity. | |||||||||||||
| Medical condition: Obesity | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) PT (Completed) NO (Completed) SK (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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