- Trials with a EudraCT protocol (3,042)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
3,042 result(s) found for: BMI.
Displaying page 1 of 153.
EudraCT Number: 2021-004919-11 | Sponsor Protocol Number: FLAIR-i | Start Date*: 2022-05-03 | ||||||||||||||||
Sponsor Name:Donders Institute for Brain, Cognition and Behaviour, Radboud University | ||||||||||||||||||
Full Title: The effect of colchicine on Food-reLAted effort-based decision making in brain and behavIouR in overweight and obesity: the FLAIR-i study. | ||||||||||||||||||
Medical condition: Low-grade inflammation in obesity | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006352-36 | Sponsor Protocol Number: VPN-10-18 | Start Date*: 2013-04-11 | ||||||||||||||||
Sponsor Name:Lithuanian University of Health Sciences, Endocrinology Department | ||||||||||||||||||
Full Title: Obesity in children and adolescents: complications, associated risks and early intervention (lifestyle changes and insulin sensitivity improving medicine (metformin) effectiveness and safety evalua... | ||||||||||||||||||
Medical condition: The aim of our study is to establish the effectivenes and safety of metformin use in pediatric obese population; to assess the prevalence of insulin resistance, metabolic syndrome, polycystic ovary... | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000775-42 | Sponsor Protocol Number: RIMON_L_00075 | Start Date*: 2007-12-27 | |||||||||||
Sponsor Name:University Hospital Tübingen | |||||||||||||
Full Title: Effects of Rimonabant on Liver Fat, Visceral Adipose Tissue Mass and early Markers of CardioDiabetes in obese Subjects with the Metabolic Syndrome – a randomized, double-blind clinical trial | |||||||||||||
Medical condition: overweight, obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 2019-002274-31 | Sponsor Protocol Number: U1111-1215-8606 | Start Date*: 2020-12-16 | |||||||||||
Sponsor Name:Department of Biomedical Sciences, University of Copenhagen | |||||||||||||
Full Title: Young adults with early-onset obesity treated with semaglutide | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000907-13 | Sponsor Protocol Number: 2007-24-001 | Start Date*: 2007-11-13 | ||||||||||||||||||||||||||
Sponsor Name:MUW, Innere Med III, Abt.für Endokrinologie & Stoffwechsel | ||||||||||||||||||||||||||||
Full Title: The impact of Rimonabant in overweight women with prior gestational diabetes | ||||||||||||||||||||||||||||
Medical condition: Rimonabant has been shown to reduce body weight and improve cardiovascular risk factors and metabolic control. Therefore we investigate in women with previous gestational diabetes and impaired glu... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005628-16 | Sponsor Protocol Number: Uni-Koeln-1473 | Start Date*: 2012-08-06 |
Sponsor Name:University of Cologne | ||
Full Title: FTO-genotype dependent weight reduction under treatment with bromocriptin in obese patients | ||
Medical condition: Obesity with BMI ≥ 30kg/m² | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002199-88 | Sponsor Protocol Number: NN8022-1922 | Start Date*: 2008-12-15 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Effect of liraglutide on body weight in overweight or obese subjects with type 2 diabetes A 56 week randomised, double-blind, placebocontrolled, three armed parallel group, multi-centre, multina... | ||||||||||||||||||
Medical condition: Obesity and overweight | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) ES (Completed) FR (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003380-35 | Sponsor Protocol Number: EX9536-4388 | Start Date*: 2018-10-05 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: SELECT - Semaglutide effects on cardiovascular outcomes in people with overweight or obesity | ||||||||||||||||||
Medical condition: Overweight Obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) DK (Completed) FI (Completed) IE (Completed) PT (Completed) GB (GB - no longer in EU/EEA) LV (Completed) NL (Completed) CZ (Completed) HU (Completed) BE (Completed) AT (Completed) SE (Completed) HR (Completed) NO (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002470-86 | Sponsor Protocol Number: 20190218 | Start Date*: 2023-05-08 | ||||||||||||||||
Sponsor Name:Amgen Inc. | ||||||||||||||||||
Full Title: A Phase 2 Randomized, Placebo-controlled, Double-blind, Dose-ranging Study to Evaluate the Efficacy, Safety and Tolerability of AMG 133 in Adult Subjects With Overweight or Obesity, With or Without... | ||||||||||||||||||
Medical condition: Overweight and Obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) HU (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010116-15 | Sponsor Protocol Number: CTU 052 D | Start Date*: 2010-05-31 |
Sponsor Name:RIEMSER Arzneimittel AG | ||
Full Title: A multicentre double blind placebo controlled clinical dose- finding study for three doses of Antiadipositum X 112 T® (Cathine-hydrochloride) vs. placebo in 240 patients with a body mass index (BMI... | ||
Medical condition: diet-related obesity diagnosed by BMI of 30 to 40 kg/m² or diet-related obesity diagnosed by BMI of 27 to 40 kg/m² in patient with coexisting risk factors like hyperlipidaemia, type 2 diabetes mell... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003426-24 | Sponsor Protocol Number: CTU079G | Start Date*: 2013-02-13 |
Sponsor Name:Riemser Pharma GmbH | ||
Full Title: A multicentre double blind placebo controlled clinical trial to assess efficacy and safety of Alvalin® (cathine hydrochloride) vs. placebo in 265 obese patients/group with a body mass index (BMI) b... | ||
Medical condition: diet-related obesity diagnosed by BMI of 30 to 45 kg/m² | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-004107-32 | Sponsor Protocol Number: RM-493-030 | Start Date*: 2023-01-23 |
Sponsor Name:Rhythm Pharmaceuticals, Inc. | ||
Full Title: A Phase 2, Open-Label 20-Week Study to Evaluate the Safety and Efficacy of Setmelanotide in Subjects with Hypothalamic Obesity | ||
Medical condition: Hypothalamic Obesity | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-002868-14 | Sponsor Protocol Number: CLIK066B2201 | Start Date*: 2017-04-18 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A randomized, double-blind, dose-finding study to evaluate the change in weight after 24 weeks treatment with 8 doses of LIK066 compared to placebo in obese or overweight adults, followed by 24 wee... | ||||||||||||||||||
Medical condition: change in weight in obese or overweight adults | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) CZ (Completed) AT (Completed) HU (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000882-41 | Sponsor Protocol Number: NN9535-4984 | Start Date*: 2022-07-27 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Investigation of once-weekly semaglutide s.c. dose-response in patients with type 2 diabetes and overweight – a participant- and investigator-blinded and sponsor open-label study | ||||||||||||||||||
Medical condition: Diabetes Mellitus, Type 2 Overweight | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) GR (Trial now transitioned) PL (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2019-003940-61 | Sponsor Protocol Number: MINT | Start Date*: 2020-12-07 |
Sponsor Name:Uppsala county council | ||
Full Title: Metformin Intervention in children and adolescents with obesity. A parallel, three arms, randomized, 6 months, multi-center study with metformin extended release (XR) plus lifestyle or metformin i... | ||
Medical condition: Children and Adolscents with obesity | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003726-32 | Sponsor Protocol Number: NN9536-4378 | Start Date*: 2018-08-22 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Two-year effect and safety of semaglutide 2.4 mg once-weekly in subjects with overweight or obesity | ||||||||||||||||||
Medical condition: Obesity Overweight | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002953-11 | Sponsor Protocol Number: NN9932-4737 | Start Date*: 2021-06-23 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Efficacy and safety of oral semaglutide 50 mg once daily in subjects with overweight or obesity | ||||||||||||||||||
Medical condition: Obesity Overweight | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) FR (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001731-40 | Sponsor Protocol Number: UMCN-ONCO-201301 | Start Date*: 2013-08-26 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Influence of exceptional patient characteristics on everolimus exposure | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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