Hypoglycemic Potential of Garcinia Cambogia (Garcinia Gummi-gutta (L.) N.Robson) Rind Powder Among Pre-diebetic Obese Patients
1 other identifier
interventional
90
1 country
1
Brief Summary
Garcinia cambogia, rich in hydroxycitric acid (HCA), has been suggested to promote weight loss and improve metabolic parameters. Evidence regarding its efficacy in pre-diabetic obese adults remains limited. Objective: To evaluate the effects of Garcinia cambogia rind powder supplementation on anthropometric, glycemic, lipid, hepatic, and renal parameters in pre-diabetic obese adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 11, 2026
CompletedFirst Posted
Study publicly available on registry
February 18, 2026
CompletedFebruary 18, 2026
October 1, 2025
3 months
February 11, 2026
February 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Weight
12 weeks
Secondary Outcomes (2)
Lipid profile
12 weeks
fasting glucose
12 weeks
Study Arms (3)
Placebo group
PLACEBO COMPARATORStarch capsule once a day
T1
EXPERIMENTAL100mg/day of Garcinia cambogia rind powder
T2
EXPERIMENTAL200mg/day of Garcinia cambogia rind powder
Interventions
Eligibility Criteria
You may qualify if:
- Participants of both genders were included if they were aged 30-60 years,
- body mass index (BMI) ≥30 kg/m²,
- Individuals with HbA1c levels ranging from 5.7% to 10% were selected, .indicating pre-diabetic to diabetic status. Participants were required to have a .body mass index (BMI) of 25 kg/m² or higher
You may not qualify if:
- Participants who were diagnosed with type 1, pregnant or lactating,
- chronic liver, kidney, or cardiovascular disease,
- history of hepatotoxicity or gastrointestinal disorders,
- using weight-loss supplements, steroids, or lipid-lowering drugs, or had a known allergy to Garcinia cambogia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sana Noreen
Lahore, 54000, Pakistan
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 11, 2026
First Posted
February 18, 2026
Study Start
September 1, 2025
Primary Completion
November 24, 2025
Study Completion
January 1, 2026
Last Updated
February 18, 2026
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share