To Assess the Efficacy of CitruSlim® on Body Composition as Well as Metabolic and Hormonal Factors in Overweight and Obese Individuals
Completed · Not applicable · Has a placebo group
Conditions studied: Overweight and Obesity
In brief
CitruSlim® can promote healthy weight loss by promoting anabolic state during weight loss programs, prevent the body from storing fat, reduce appetites and maintain healthy cholesterol and blood glucose level during weight loss program. This study focuses to prove the efficacy and safety of the product in a population of overweight and obese individual.
Key facts
- Study ID
- NCT03973086
- Run by
- Vedic Lifesciences Pvt. Ltd.
- People needed
- 97
- Starts
- 2019-06-04
- Expected to finish
- 2020-09-18
- Last updated by the study team
- 2021-04-12
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male and female participants with the age of ≥18 and ≤ 60 years of age.
- BMI of ≥25 - ≤ 35 kg/m2
- Waist circumference:India: Men: > 94 cm (37 inches), Women: >80 cm (31.5 inches) USA: Men: > 102 cm (40 inches), Women: >89 cm (35 inches)
- Triglycerides >150 mg/dL
- Blood pressure: Systolic: ≥130 mm Hg and/or Diastolic: ≥85 mm Hg
- Fasting blood glucose ≥ 100 mg/ dl
- Low HDL level: Men: < 40 mg/dL, Women: < 50 mg/dL
- Ready to give voluntary, written, informed consent to participate in the study.
You may not qualify if…
- Participants meeting any of the following criteria will be excluded from the trial:
- Current smoker.
- Inability to walk independently.
- Presence of unstable, acutely symptomatic, or life-limiting illness.
- Neurological conditions causing functional or cognitive impairments
- Unwillingness or inability to be randomized to one of three intervention groups.
- Bilateral hip replacements.
- Exposure to any non-registered drug product within 3 months prior to the screening visit.
- Unable/unwillingness to complete study specific diaries (digital/paper-based).
Where it is running
- Reveal — Bradenton, Florida, United States
Full record on ClinicalTrials.gov
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