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
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