跳至主要内容
临床试验/CTRI/2017/03/008045
CTRI/2017/03/008045招募中2 期

A randomized, double blind, placebo controlled, clinical study to evaluate the efficacy and safety of Curcuma caesia for weight management in obesity.

Sami Labs Limited0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
60

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 Male and/or female patients.
  • 2 Age between 20 to 60 years.
  • 3 BMI between > 35 to 40 Kg/m2.
  • 4 Willing to come for regular follow -up visits.
  • 5 Able to give written informed consent.

排除标准

  • 1 Intake of over the counter weight loss agents, centrally acting appetite suppressants in the previous six months.
  • 2 Pathophysiologic/ genetic syndromes associated with obesity (Cushingâ??s syndrome, Turnerâ??s syndrome, Praderwilli syndrome).
  • 3 Patients with evidence of malignancy.
  • 4 Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants, anticholinergic, etc. or any other drugs that may have an influence on the outcome of the study.
  • 5 Symptomatic patient with clinical evidence of Heart failure.
  • 6 History of HIV and other viral infections.
  • 7 Prior surgical therapy for obesity
  • 8 History of hypersensitivity to any of the herbal extracts or dietary supplement.
  • 9 Pregnant / lactating woman.
  • 10 Patients who have completed participation in any other clinical trial during the past six (06) months.
  • 11 Any other condition which the Principal Investigator thinks may jeopardize the study.

研究者

发起方
Sami Labs Limited

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