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Effectiveness of IRK-19® on Body Weight Control

Effectiveness of IRK-19® on Body Weight Control

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05542160
Enrollment
50
Registered
2022-09-15
Start date
2022-10-01
Completion date
2024-06-30
Last updated
2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome, Overweight

Brief summary

This randomized, double-blind, placebo-controlled, and parallel clinical study aims to investigate the effectivness of a pumpkin seed extract (IRK-19®) on weight management.

Interventions

DIETARY_SUPPLEMENTPumpkin seed extract (IRK-19)

Placebo: Dietary fiber powder, two capsules/day (600 mg/day), continued use for 3 months Treatment: Pumpkin seed extract powder, two capsules/day (600 mg/day), continued use for 3 months

Sponsors

Taipei Medical University WanFang Hospital
CollaboratorOTHER
Greenyn Biotechnology Co., Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

1. BMI: 25-30 kg/m2 2. Waistline circumference: ˃ 80 cm

Exclusion criteria

1. Pregnant women or preparing for pregnancy. 2. Lactating women. 3. Women gave birth 6 months before the study. 4. Subject uses diuretic, corticosteroids, anti-depressant medications, or antipsychotic medications. 5. Subject has undertaken obesity-related surgeries within one year prior to the study or other surgeries within six months prior to the study. 6. Change of body weight of subject is over 5% within 3 months before the study. 7. Subject has serious diseases (e.g., cardiovascular diseases). 8. Cancer patient. 9. Subject has engaged in another study within 3 months before the study. 10. Subject uses another dietary supplement related to weight management during the study.

Design outcomes

Primary

MeasureTime frameDescription
BiochemistryWeek 0Total cholesterol
Anthropometric measurementWeek 0Body weight
Body composition analysisWeek 0Body fat

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026