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Clinical Trials/NCT05451927
NCT05451927CompletedNot Applicable

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

Hafiza Aisha Sadiqa2 sites in 1 country72 target enrollmentStarted: October 27, 2022Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
72
Locations
2
Primary Endpoint
Body weight
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Outcomes

Primary Outcomes

Body weight

Time Frame: 3 months

change in body weight

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hafiza Aisha Sadiqa
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Hafiza Aisha Sadiqa

Student

University of the Punjab

Study Sites (2)

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Trial to Examine the Effect of Natural... | Clinical Trial