- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
69 result(s) found for: Abdominal obesity.
Displaying page 1 of 4.
EudraCT Number: 2006-001716-71 | Sponsor Protocol Number: RIMON_C_01346 | Start Date*: 2006-09-12 | |||||||||||
Sponsor Name:sanofi aventis Groupe | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE BLIND, TWO ARM, PARALLEL, PLACEBO CONTROLLED STUDY OF RIMONABANT 20MG EFFECT ON HIGH DENSITY LIPOPROTEIN KINETICS IN PATIENTS WITH ABDOMINAL OBESITY AND ADDITIONAL CARDIOMETABO... | |||||||||||||
Medical condition: PATIENTS WITH ABDOMINAL OBESITY AND ADDITIONAL CARDIOMETABOLIC RISK FACTORS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001711-30 | Sponsor Protocol Number: RIMON_R_00961 | Start Date*: 2006-10-11 | |||||||||||
Sponsor Name:sanofi aventis Groupe | |||||||||||||
Full Title: A Pan-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 impaired fast... | |||||||||||||
Medical condition: abdominally obese patients with impaired fasting blood glucose with or without other comorbidities | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) BE (Completed) PT (Prematurely Ended) CZ (Completed) SI (Completed) FR (Completed) NL (Prematurely Ended) NO (Completed) FI (Prematurely Ended) SE (Prematurely Ended) DK (Prematurely Ended) LT (Prematurely Ended) HU (Completed) SK (Completed) GR (Completed) AT (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001361-16 | Sponsor Protocol Number: PI-11-PR-REGIMBEAU-2 | Start Date*: 2013-11-21 | ||||||||||||||||
Sponsor Name:CHU AMIENS | ||||||||||||||||||
Full Title: Randomized prospective clinical study evaluating the usefulness of fibrin glue (TISSEEL) to prevent gastric fistula, intra abdominal haemorrhage and intra abdominal loco regional collections after ... | ||||||||||||||||||
Medical condition: morbid obesity sleeve gastrectomy | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015982-29 | Sponsor Protocol Number: UMCU-Vasc-14A | Start Date*: 2010-07-27 | ||||||||||||||||||||||||||
Sponsor Name:University Medical Center Utrecht | ||||||||||||||||||||||||||||
Full Title: A randomized, placebo-controlled, double blind, 4-period, cross-over trial, to study the effects of aliskiren, hydrochlorothiazide and moxonidine on endothelial dysfunction in obesity related hyper... | ||||||||||||||||||||||||||||
Medical condition: Hypertension in subjects with abdominal obesity and the metabolic syndrome | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002077-31 | Sponsor Protocol Number: RIMON_L_01814 | Start Date*: 2008-09-09 | |||||||||||
Sponsor Name:SANOFI-AVENTIS S.P.A | |||||||||||||
Full Title: Effects of Rimonabant on urinary albumin excretion rate on the components of the metabolic syndrome in patients with type 2 diabetes mellitus and microalbuminuria on background ramipril treatment. ... | |||||||||||||
Medical condition: Abdominal obese patients with type 2 diabetes mellitus and microalbuminuria. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009278-29 | Sponsor Protocol Number: S51477 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:UZ Leuven | ||||||||||||||||||||||||||||
Full Title: Follow-up studie: Metformin therapie bij kinderen en adolescenten met neurogene of neuromusculaire aandoeningen | ||||||||||||||||||||||||||||
Medical condition: Neuromuscular and neurological diseases, associated with obesity and insulin resistance | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002951-33 | Sponsor Protocol Number: RIMON_L_01031 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:sanofi-aventis, S.A. | |||||||||||||
Full Title: A 12-month multicentre, randomised, double-blind, placebo-controlled study with two parallel groups to assess the effects of rimonabant 20 mg in patients with abdominal obesity and microalbuminuria... | |||||||||||||
Medical condition: Patients with abdominal obesity, with type 2 diabetes mellitus or dyslipidaemia, with or without other cardiometabolic risk factors. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005779-86 | Sponsor Protocol Number: GFT505-208-3 | Start Date*: 2008-12-26 | ||||||||||||||||
Sponsor Name:GENFIT | ||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy and Safety of GFT505 (80 mg) orally administered once daily for 28 days in atherogenic dyslipidaemic patients with abdominal obesity. A double blind, placebo-... | ||||||||||||||||||
Medical condition: Atherogenic dyslipidaemic patients with abdominal obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004337-41 | Sponsor Protocol Number: GFT505-207-2 | Start Date*: 2008-01-11 | ||||||||||||||||
Sponsor Name:GENFIT | ||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy and Safety of GFT505 orally administered once daily (30 mg) for 28 days in atherogenic dyslipidaemic patients with abdominal obesity. A double blind, placebo-... | ||||||||||||||||||
Medical condition: Atherogenic dyslipidaemic patients with abdominal obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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: 2007-004124-20 | Sponsor Protocol Number: 200701234 | Start Date*: 2007-10-10 | |||||||||||
Sponsor Name:LUMC | |||||||||||||
Full Title: Doxycycline for Stabilization of Abdominal Aortic Aneurysms | |||||||||||||
Medical condition: Abdominal aortic aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002568-27 | Sponsor Protocol Number: PM-C-0172 | Start Date*: 2006-05-08 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Groupe | |||||||||||||
Full Title: A randomized, double blind, two-arm placebo controlled, 12-Month study of the effects of rimonabant 20mg once daily on the amount and the activity of visceral fat in abdominally obese patients with... | |||||||||||||
Medical condition: Abdominally obese patients with metabolic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DK (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011003-23 | Sponsor Protocol Number: GFT505-209-4 | Start Date*: 2009-05-28 | ||||||||||||||||
Sponsor Name:GENFIT | ||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy and Safety of GFT505 (80mg) orally administered once daily for 35 days in patients presenting with impaired glucose tolerance and abdominal obesity. A double ... | ||||||||||||||||||
Medical condition: patients presenting with impaired glucose tolerance and abdominal obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023219-32 | Sponsor Protocol Number: GFT505-210-6 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:GENFIT | |||||||||||||||||||||||
Full Title: A Pilot study to evaluate the Efficacy of GFT505 (80mg) orally administered once daily for 8 weeks on insulin sensitivity and hepatic glucose production using a glucose clamp technique and Safety i... | |||||||||||||||||||||||
Medical condition: Patients with insulin resistance and abdominal obesity | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003244-30 | Sponsor Protocol Number: no sponsor | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Rijnstate Hospital | |||||||||||||
Full Title: Diazoxide-Mediated Insulin Suppression in Hyperinsulinemic Obese Men, part III. | |||||||||||||
Medical condition: Hyperinsulinemic men with BMI 30-35 kg/m2 | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2005-004566-16 | Sponsor Protocol Number: CSPP100A2238 | Start Date*: 2007-03-12 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: Part 1: An open Label Pilot Study to Determine Interstitial and Tissue Concentrations of Aliskiren and Effects on the Renin-Angiotensin System (RAS) in Fat and Skeletal Muscle of Hypertensive Patie... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-000803-32 | Sponsor Protocol Number: AN05/6880 | Start Date*: 2005-08-09 |
Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
Full Title: Does the infiltration of Levobupivacaine into the rectus abdominus muscle ( Rectus Sheath Block) improve post-operative analgesia following open gastric bypass for morbid obesity? | ||
Medical condition: Morbid Obesity. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000567-28 | Sponsor Protocol Number: TROTA-1 | Start Date*: 2007-09-01 | |||||||||||
Sponsor Name:Fundació Clínic Recerca Biomédica | |||||||||||||
Full Title: Eficacia de tungstato sódico por vía oral a una dosis fija de 200 mg por día sobre la pérdida de peso en pacientes con obesidad grado I y grado II. | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012124-85 | Sponsor Protocol Number: 0816302 | Start Date*: 2009-07-27 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: Etude exploratoire de l’effet d’un traitement par acide nicotinique sur l’inflammation du tissu adipeux sous cutané | |||||||||||||
Medical condition: processus de l'inflammation du tissu adipeux et des mécanismes de l'insulinorésistance | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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