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临床试验/EUCTR2007-000775-42-DE
EUCTR2007-000775-42-DE进行中(未招募)不适用

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

niversity Hospital Tübingen0 个研究点开始时间: 2007年9月19日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Age: 18 - 70 years, inclusive
  • Gender: male, female
  • BMI: 27- 45
  • Metabolic syndrome according to the ATP III criteria (any 3 of the following):
  • Abdominal obesity: waist circumference > 102 cm (men), > 88 cm (women)
  • Triglyzeride 150 mg/dl
  • HDL < 40 mg/dl (men), < 50 mg/dl (women)
  • Blood pressure 130/ 85 mmHg
  • Fasting glucose 110 mg/dl
  • Or impaired fasting glucose 5.6 mmol/l and 7.0 mmol/l
  • Or impaired glucose tolerance : 2-h-glucose (75g OGTT) 7.8 mmol/l and 11.1 mmol/l
  • Stable weight (+ 5 kg) in the last 6 months
  • No lifestyle intervention study in the last 6 months
  • Willing and able to complete screening and study procedures, as described in the protocol
  • Signed written informed consent to participate in the study
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • General health problems (e.g. cancer, cardiovascular events in the past 12 months)
  • Significant findings indicating: cardiovascular, endocrine, pulmonary, neurologic, psychiatric, gastrointestinal, hepatic, hematologic, renal, or dermatologic disease
  • Any of the following blood examination results:
  • Positive hepatitis-B-surface-antigen
  • Positive hepatitis-C antibody
  • Positive HIV-antibodies
  • Abnormal thyrotropin level
  • GPT, GOT > 2.5 times the upper limit of the normal range
  • Haemoglobin levels < 11 g/dl
  • Neutrophil levels < 1500 /mm3
  • Platelet levels < 100.000/ mm3
  • Creatinine level > 150 ?mol/l
  • Any positive history of marijuana or hashish use, no matter how long ago or a positive drug test for marijuana or hashish
  • Acutal misuse of other drugs
  • Severe depression (requiring hospitalization or indicated by a suicidal attempt)
  • Mild or severe depression according to the depression questionnaire (MDI) at screening
  • Antidepressive pharmacological treatment
  • Treatment for epilepsy and eating disorder or a malignant disease
  • Diabetes mellitus (type 1 or 2)
  • Pharmacological treatment of dyslipidemia within 6 weeks before screening
  • Systolic blood pressure > 165 mmHg
  • Diastolic blood pressure > 105 mmHg
  • Hypersensivity to the active substance or to any of the exipients (see SPC appendix 17.1)
  • Exclusion criterias for MRT-, 1HMRS- examinations: non-compliance, pace maker, cochlea implant, nerve stimulators, magnetic vascular clips, metallic heart valve or other contraindications for MRT-, 1HMRS- examinations
  • Patients with lactose intolerance, rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose
  • Regular use potent CYP3A4 inhibitiors: ketoconazole, itraconazole, indinavir, saquinavir, ritonavir, nelfinavir, lopinavir (protease inhibitors), delavirdin, erythromycin, telithromycin, clarithromycin, nefazodone, cimetidine, fluoxetine, fluvoxamine, paroxetine, sertaline, naringenine (grape fruit juice), verapamile
  • Potent CYPA3-Inducers: rifampicin, phenytoin, phenobarbital, carbamazepine, St John’s wort
  • Any Medication containing cannabis

研究者

发起方
niversity Hospital Tübingen

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