About this trial
A Randomized, Double-Blind, Placebo-Controlled, Two-Arm, Single-Centre, Clinical Study to Evaluate the Safety and Efficacy of Intake of ACV Moringa on the Degree of Weight Change in Overweight and Class I Obese Study Participants
Eligibility criteria
Qualifiers
Age: 18- 65 years (both inclusive) at the time of consent.
Sex: Males and non-pregnant/non-lactating females (preferably equal number of males and females).
Females of childbearing potential must have a self-reported negative urine pregnancy.
Female of childbearing potential must have a reported negative pregnancy during screening and the end of the study
Disqualifiers
Subjects BMI is between less than 25 and greater than 35 kg/m2.
Subjects having past or present history or clinically significant findings indicating cardiovascular disease, type 2 diabetes mellitus, hypertension, endocrine, pulmonary, neurological or psychological disorders, hypo or hyperthyroidism and renal disorders.
Subjects with a history of gastrointestinal disorders, including chronic gastritis, gastric discomfort, or any diagnosed gastrointestinal conditions.
Subjects having drug and alcohol abuse.
Trial design
Treatments tested in this trial
- ACV Moringa Effervescent Tablets 4.3 g
- Placebo Effervescent Tablets 4.3 g
Treatment groups
Locations
Sponsors and collaborators
NovoBliss Research Pvt Ltd
Lead sponsor
Zywie Ventures Pvt Ltd
Collaborator