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临床试验/CTRI/2021/12/038704
CTRI/2021/12/038704招募中未知

Efficacy and safety of 3% Arjunoglucoside on individuals who are at higher risk of cardiovascular disease - A randomized, double-blind, placebo controlled clinical study.

SamiSabinsa Group Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方

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 female of 35 to 65 years old, both inclusive.
  • 2.Atherogenic index of plasma > 0.1
  • 3.BMI >= 30 kg/m2
  • 4.Total cholesterol > 200mg/dL; LDL > 150mg/dL; Serum Triglyceride > 150mg/dL; HDL Cholesterol < 40;
  • 5.Blood Pressure - Systolic 140-159 mm Hg and/or diastolic 90-99 mm Hg ( Grade 1 hypertension)
  • 6.Females with child-bearing potential who agree to use barrier method of contraception throughout the study period.
  • 7.Patients must be willing to come for regular follow-up visits.
  • 8.Willing to sign informed consent.

排除标准

  • 1.Pregnant or lactating or female having the intention to be pregnant within next three months.
  • 2.Do not agree to stop Smoking & Alcohol intake during the study duration
  • 3.BMI > 40 kg/m2
  • 4.Subjects having history of diabetes (Type I or Type II)
  • 5.Fasting Blood Glucose >= 126 mg/dl and HbA1c >= 7%.
  • 6.Patients undergoing any other regimen apart from the prescribed standard management
  • 7.Having untreated BP of systolic < 140 mmHg & >= 160 mmHg and diastolic < 90 mmHg & > 100 mmHg.
  • 8.Patients having Lactose intolerance.
  • 9.Liver dysfunction (serum bilirubin > 1.5 times upper limit of normal or serum transaminase > 2 times upper limit of normal
  • 10.Patients having neurodegenerative & major psychiatric disorders
  • 11.Subjects with concurrent serious hepatic disorder (defined as Aspartate Amino Transferase (AST) and/or Alanine Amino Transferase (ALT), Total Bilirubin, Alkaline Phosphatase (ALP) >2 times upper normal limit) or Renal Disorders (defined as S. Creatinine >1.2mg/dL for females or >1.4 mg/dL for males and EGFR of 60 or less)
  • 12.A history of significant multiple and/or severe allergies or anaphylactic reactions
  • 13.Patient with known history of hypersensitivity to the investigational product
  • 14.Patient has participated in any clinical trial within last 3 months
  • 15.Any other condition which the Principal Investigator thinks may jeopardize the study

研究者

发起方
SamiSabinsa Group Limited

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