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

N/ACompletedNCT05451927

Hafiza Aisha Sadiqa72 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

QUADRUPLE

Enrollment

Conditions

Overweight and Obesity

Interventions

Phaseolus VulgarisDIETARY_SUPPLEMENT

Weight loss

PlaceboDIETARY_SUPPLEMENT

Placebo

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (2)

Akhuwat Medical Centre

Lahore, Punjab Province, Pakistan

Niazi Medical Centre

Lahore, Punjab Province, Pakistan

Outcomes

Primary Outcomes

Body weight

change in body weight

Time frame: 3 months

Data from ClinicalTrials.gov

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