- Trials with a EudraCT protocol (3,388)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
3,388 result(s) found for: Body Weight.
Displaying page 1 of 170.
EudraCT Number: 2008-003395-22 | Sponsor Protocol Number: W3600586 | Start Date*: 2008-09-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: The Effects of Weight Reduction with Orlistat vs. Placebo on Changes in Body Composition | |||||||||||||
Medical condition: Weight Loss | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006986-10 | Sponsor Protocol Number: W3680604 | Start Date*: 2009-02-04 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: A Study to Assess the Pharmacologic Equivalence of Two Orlistat Dosage Forms | |||||||||||||
Medical condition: Weight loss | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004797-79 | Sponsor Protocol Number: W2660371 | Start Date*: 2007-09-28 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: A Study to Assess the Pharmacologic Equivalence of Two Orlistat Dosage Forms | |||||||||||||
Medical condition: Weight loss | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000677-31 | Sponsor Protocol Number: STH15216 | Start Date*: 2011-09-16 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Testosterone Replacement in Young Male cancer Survivors | |||||||||||||
Medical condition: Borderline low levels of testosterone in male cancer survivors who have previously had leukaemia, lymphoma or testicular cancer. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004275-70 | Sponsor Protocol Number: GPD-01-01 | Start Date*: 2016-01-08 |
Sponsor Name:Gene PreDiT SA | ||
Full Title: Influence of single nucleotide polymorphisms of carboxypeptidase D (CPD) gene on body weight and fat mass reduction by perindopril in obese subjects: A phase II, multicenter, double-blind study. | ||
Medical condition: Body weight and fat mass reduction by perindopril in obese subjects | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-002145-15 | Sponsor Protocol Number: NOK0023 | Start Date*: 2023-10-31 |
Sponsor Name:Nederlandse Obesitas Kliniek | ||
Full Title: Applying Mysimba in patients with weight regain after bariatric surgery | ||
Medical condition: Weight regain post bariatric surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004866-15 | Sponsor Protocol Number: EMI111963 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: A Longitudinal MRI Study of Changes in Regional Body Composition During Orlistat (60mg)-Assisted Dieting | |||||||||||||
Medical condition: Weight loss | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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 (Ongoing) NO (Ongoing) SK (Ongoing) HU (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004998-13 | Sponsor Protocol Number: LP0160-1329 | Start Date*: 2020-06-02 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: Adjustable brodalumab dosage regimen compared with standard brodalumab treatment for 52 weeks in subjects with moderate-to-severe plaque psoriasis and ≥120 kg body weight | |||||||||||||
Medical condition: moderate-to-severe plaque psoriasis and a body weight ≥120 kg. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) DE (Ongoing) DK (Prematurely Ended) GB (GB - no longer in EU/EEA) IT (Ongoing) HU (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003569-91 | Sponsor Protocol Number: NL62896 | Start Date*: 2017-12-08 |
Sponsor Name:Hagaziekenhuis | ||
Full Title: The effect of body weight on trough concentrations of DOACs in patients. | ||
Medical condition: No medical condition will be investigated. This study will only investigate the effect of body weight on through concentrations of direct oral anticoagulants (DOACs) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002364-29 | Sponsor Protocol Number: 015 | Start Date*: 2005-09-02 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: A Two Year Study to Assess the Efficacy, Safety, and Tolerability of MK-0364 in Obese Patients | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) NO (Prematurely Ended) DK (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000956-32 | Sponsor Protocol Number: 20022012 | Start Date*: 2012-06-28 |
Sponsor Name:St. Antonius Ziekenhuis | ||
Full Title: Pharmacokinetics of intravenous acetaminophen and its metabolites in morbidly obese patients | ||
Medical condition: Morbid obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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: 2006-004366-14 | Sponsor Protocol Number: MK-0364 012 | Start Date*: 2006-11-13 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: Full title of the trial A Study to Assess the Efficacy and Tolerability of MK-0364 in Maintaining Weight Loss Induced by Diet in Obese Patients Followed by a 1-Year Extension | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002816-19 | Sponsor Protocol Number: Frax001 | Start Date*: 2012-10-25 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous injection of 5700 IU nadroparin in morbidly obese p... | ||
Medical condition: patients; perioperative in bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
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: 2014-003432-39 | Sponsor Protocol Number: D1690L00016 | Start Date*: 2014-11-19 | |||||||||||
Sponsor Name:Dept of Medical Sciences, Clinical Diabetes and Metabolism, Uppsala University | |||||||||||||
Full Title: A 24-week, single centre, randomized, parallel-group, double-blind, placebo controlled Phase II study to evaluate the efficacy on body weight of dapagliflozin 10 mg once daily in combination with e... | |||||||||||||
Medical condition: Obesity defined as body mass index (BMI) 30-45 kg/m2 Obesity related metabolic disorders | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002235-60 | Sponsor Protocol Number: NN9536-7545 | Start Date*: 2023-02-24 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Effect and safety of semaglutide 7.2 mg once-weekly in participants with obesity and type 2 diabetes | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Ongoing) SK (Ongoing) HU (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000220-19 | Sponsor Protocol Number: 2.2 | Start Date*: 2020-09-24 |
Sponsor Name:Verein zur Förderung von Wissenschaft und Forschung an der 1. Med. Abteilung der Krankenanstalt Rudolfstiftung | ||
Full Title: Comparing effects of weight loss by Liraglutide 3.0 mg with conventional liver fasting in non-alcoholic fatty liver disease before bariatric surgery | ||
Medical condition: Obesity and NAFLD can increase the risk and complexity of bariatric surgery up to 20%. Reducing the weight and liver size before bariatric surgery improves the operation area and reduces complicati... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005435-75 | Sponsor Protocol Number: U1111-1261-1912 | Start Date*: 2022-07-21 | ||||||||||||||||
Sponsor Name:NOVO NORDISK. S.P.A. | ||||||||||||||||||
Full Title: Efficacy and safety of cagrilintide s.c. 2.4 mg in combination with semaglutide s.c. 2.4 mg (CagriSema s.c. 2.4 mg/2.4 mg) once-weekly in participants with overweight or obesity | ||||||||||||||||||
Medical condition: Obesity, Overweight | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) NL (Ongoing) DK (Ongoing) FI (Ongoing) ES (Ongoing) PL (Ongoing) BG (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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