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NCT05451927 Clinical Trial

Trial to Examine the Effect of Natural Anti- Obesity Agent (Phaseolus Vulgaris) Among Women of Lahore

Overweight and Obesity Clinical Trial

— PVE-AO  

Official title:
A Randomized Double Blind Study to Examine the Effect of Natural Anti-obesity Agent Among Women of Lahore

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05451927
Other study ID # RCT012022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 27, 2022
Est. completion date December 30, 2023

Study information
Verified date April 2024
Source University of the Punjab
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 72
Est. completion date December 30, 2023
Est. primary completion date December 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• Phaseolus Vulgaris
Weight loss
• Placebo
Placebo

Locations
Country Name City State
Pakistan Akhuwat Medical Centre Lahore Punjab
Pakistan Niazi Medical Centre Lahore Punjab

Sponsors (2)
Lead Sponsor Collaborator
Hafiza Aisha Sadiqa University of the Punjab

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Body weight change in body weight 3 months
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