Trial to Examine the Effect of Natural Anti- Obesity Agent (Phaseolus Vulgaris) Among Women of Lahore
Not Applicable
Completed
- Conditions
- Overweight and Obesity
- Interventions
- Dietary Supplement: Phaseolus VulgarisDietary Supplement: Placebo
- Registration Number
- NCT05451927
- Lead Sponsor
- Hafiza Aisha Sadiqa
- Brief Summary
This double-blind randomized placebo-controlled trial will test the hypothesis that administration of Phaseolus Vulgaris supplementation to women in Lahore, Pakistan, who are overweight will induce the weight loss (Primary outcome) and changes in body composition (Waist circumference) secondary outcome.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 72
Inclusion Criteria
- BMI ranges from 25-40
- Consistently stable body weight for at least 6 months
- Good general health
- No ongoing drug treatment for weight reduction
- Commitment to avoid any changes in lifestyle throughout the test period
- Age between 18-45 years
- Women resident of Lahore
Exclusion Criteria
- Pregnant or breast-feeding females
- People with Type 2 diabetes
- People with any other chronic diseases
- Weight reduction treatment during the 6 months prior to the study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Phaseolus Vulgaris Phaseolus Vulgaris Three oral doses of 1000 mg Phaseolus Vulgaris daily for 3 months Placebo Placebo Three oral doses of Placebo daily for 3 months
- Primary Outcome Measures
Name Time Method Body weight 3 months change in body weight
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Akhuwat Medical Centre
🇵🇰Lahore, Punjab, Pakistan
Niazi Medical Centre
🇵🇰Lahore, Punjab, Pakistan