NCT07419074

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 24, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

February 11, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 18, 2026

Completed
Last Updated

February 18, 2026

Status Verified

October 1, 2025

Enrollment Period

3 months

First QC Date

February 11, 2026

Last Update Submit

February 11, 2026

Conditions

Keywords

Garcinia cambogia, Garcinia gummi-gutta, hypoglycemic effect, pre-diabetic, obesity, hydroxycitric acid (HCA), glucose metabolism

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 COMPARATOR

Starch capsule once a day

Dietary Supplement: Garcinia cambogia rind powder

T1

EXPERIMENTAL

100mg/day of Garcinia cambogia rind powder

Dietary Supplement: Garcinia cambogia rind powder

T2

EXPERIMENTAL

200mg/day of Garcinia cambogia rind powder

Dietary Supplement: Garcinia cambogia rind powder

Interventions

Once a day

Placebo group

Eligibility Criteria

Age30 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

Related Links

MeSH Terms

Conditions

Glucose IntoleranceObesityAdenoma, Liver Cell

Condition Hierarchy (Ancestors)

HyperglycemiaGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesOverweightOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsAdenomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

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

Locations