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临床试验/DRKS00003537
DRKS00003537已完成未知

In-vivo-quantification of both serotonin-and norepinephrin-transporter availability in obese persons without co-morbid depression using positron emission tomography (PET) and selective radio-labelled markers - comparison with healthy controls and 6 months after a multimodal treatment program - IFB-PET

niversitätsklinikum Leipzig AöRKlinik und Poliklinik für Nuklearmedizin0 个研究点目标入组 65 人开始时间: 2012年5月30日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
65

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Age between 18 and 65
  • BMI > 35 kg/m2 resp. <30 kg/m2
  • no psychotropic-medication and/or drugs for at least 8 weeks prior PET
  • written informed consent

排除标准

  • History of neurological or psychiatric diseases
  • juvenile-onset diabetes (type 1) resp. insulin dependent diabetes type 2, malignant hypertension
  • medical treatment or surgery for weight reduction less then 6 months ago
  • Structural lesions (stroke, traumatic brain injury etc.)
  • Cognitive deficits, major speech impairment, alcohol- or drug abuse (positive drug test)
  • Major mental disorders, major communicative deficiencies which inhibit an informed consent
  • neurosurgical interventions in the past
  • Epilepsy, cerebral seizures in previous medical history (or in history of the family)
  • Chronic diseases (e.g. asthma) indicating chronic medical treatment with central effect
  • Pregnancy (exclusion via urine test before the experiment)
  • Contraindications for MR imaging (e.g., implanted ferro-magnetic devices), claustrophobia

研究者

发起方
niversitätsklinikum Leipzig AöRKlinik und Poliklinik für Nuklearmedizin

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