跳至主要内容
临床试验/CTRI/2018/05/014198
CTRI/2018/05/014198已完成3 期

Clinical Evaluation of Rasanjan in the management of Sthaulya (Obesity)

A0 个研究点目标入组 48 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
A
入组人数
48

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • •1)Patients of either sex aged between 18 and 65 years.
  • •2)BMI >= 30kg/m2 and < 40kg/m2
  • •3)Willing and able to participate in the study for 60 days.

排除标准

  • •1.Patients with known history of Pathophysiologic /genetic syndromes associated with obesity (Cushingâ??s syndrome, turnerâ??s syndrome)
  • •2.Patients with known evidence of malignancy.
  • •3.Patients on prolonged medication with corticosteroids, antidepressants, anticholinergics etc or any other drugs that may have an influence on the outcome of the study.
  • •4.Patients with known history of major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, tuberculosis, Psycho- Neuro endocrine disorders etc)
  • •5.Patients who have a past history of atrial fibrillation, Acute coronary syndrome, Myocardial infarction, stroke or severe arrhythmia in the last 6 months.
  • •6.Patients with known history of serious hepatic and pulmonary disorders.
  • •7.Known cases of Alcoholics and drug abusers.
  • •8.Prior surgical therapy for obesity.
  • •9.H/o Hypersensitivity to any of the trial drugs or their ingredients.
  • •10.Pregnant or lactating women.
  • •11.Intake of over the counter weight loss agents, centrally acting appetite suppressants in the previous 6 months.
  • •12.Patients who have completed participation in any other clinical trial during the past six months.
  • •13.Any other condition which the principal investigator thinks may jeopardize the study.

研究者

发起方
A

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