跳至主要内容
临床试验/CTRI/2019/03/017953
CTRI/2019/03/017953已完成Unknown

Multicentric, randomized, four arm, double blind, parallel group study in adult hyperlipidemic, Preâ€diabetic and Normotensive subjects.

Spectrum Clinical Research Pvt Ltd2 个研究点 分布在 1 个国家目标入组 236 人开始时间: 2019年8月3日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
236
试验地点
2
主要终点
To evaluate the effect of treatment on LDL-C levels in comparison with all four groups.

研究概览

简要总结

A multicentric, randomized, four arm, double blind, parallel group study to evaluate the efficacy of Blended edible vegetable oils (Test Blend 1 and Test Blend 2) in comparison with commonly consumed oils (Control) in Hyperlipidemic, Preâ€diabetic, Normotensive adult subjects.

Subjects will be randomized to one of the four groups:

Group I – Consuming food prepared in Test Blend 1

Group II – Consuming food prepared in Palmolein oil (Control 1)

Group III – Consuming food prepared in commonly used oil (groundnut oil, sunflower oil, soyabean oil) (Control 2)

Group IV – Consuming food prepared in Test Blend 2

 Subjects would be asked to accommodate their cooking oil consumption by 500 ml./person/month.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
30.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • LDL Cholesterol levels 130-189mg/dl (ATP III Guidelines)
  • Patient with body mass index of ≥23 kg/m2 and ≤30 kg/m2
  • Untreated Dyslipidemia
  • Willingness to maintain current activity levels and follow the prescribed diet.

排除标准

  • Use of oral or injected corticosteroids or anabolic steroids 3 months prior/during the study
  • Uncontrolled thyroidism
  • Poorly controlled hypertension (resting blood pressure ≥140 mm Hg systolic and/or ≥90 mm Hg diastolic)
  • Participants on Medication/ alternative medicine/special diets for weight loss
  • Current smoker
  • Women who are pregnant, lactating, or planning to become pregnant
  • Liver disorders.

结局指标

主要结局

To evaluate the effect of treatment on LDL-C levels in comparison with all four groups.

时间窗: 90 days from Baseline Visit.

次要结局

  • To evaluate the effect of treatment on following parameters such as TC, TG, HDL, VLDL, oxLDL, hsCRP, HbA1C, Fasting & PP sugar Systolic & Diastolic BP, Mean Arterial Pressure, BMI,Waist Circumference & quality of life.(90 days from Baseline Visit.)

研究者

发起方
Spectrum Clinical Research Pvt Ltd
申办方类型
Contract research organization

研究点 (2)

Loading locations...

相似试验