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Asparagus Capsule Consumption and Blood Sugar and Lipids and Oxidative Stress

Effects of Asparagus Capsule Consumption on Blood Sugar and Lipids and Oxidative Stress in Overweight and Obese Participants

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06195813
Enrollment
44
Registered
2024-01-08
Start date
2022-12-20
Completion date
2023-09-14
Last updated
2024-01-12

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

Conditions

Asparagus Capsule Consumption

Brief summary

Participants were 44 overweight and obese persons, male and female, age 18-59 years. Participants were divided into 2 groups consisting of 23 asparagus capsules and 21 placebo capsules groups. They received health screenings including history taking, mental health questionnaire, and vital signs, height and body weight, body composition, fat distribution measurements and oral glucose tolerance test. Then, a venipuncture was conducted to determine blood glucose, insulin, lipids malondialdehyde and protein carbonyl levels.

Detailed description

The study design was cross-sectional. Participants were 44 overweight and obese persons, male and female, age 18-59 years. Participants were divided into 2 groups consisting of 23 asparagus capsules and 21 placebo capsules groups. They received health screenings including history taking, mental health questionnaire, and vital signs, height and body weight, body composition, fat distribution measurements and oral glucose tolerance test. Then, a venipuncture was conducted to determine blood glucose, insulin, lipids malondialdehyde and protein carbonyl levels. Analysis of covariance was used to analyze parameters between groups and paired t-test was used to analyze parameters intra-group.

Interventions

OTHERPlacebo capsule

Placebo capsule is categorized as other.

DIETARY_SUPPLEMENTAsparagus capsule

Asparagus capsule is categorized as dietary supplement.

Sponsors

Burapha University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Participants were randomly divided into 2 groups consisting of 23 asparagus capsules and 21 placebo capsules groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

* Man or woman, aged between 18 to 59 years * Body mass index more than 23 (Asian criteria) * No history of hypertension, diabetes, cardiovascular disease, respiratory disease, endocrine disease, neuromuscular disease, musculoskeletal disease, liver disease, renal disease, immune disease, infectious disease, or cancer * No regular intake of dietary supplements, i.e., vitamins, antioxidants * No regular smokers or alcohol drinkers (\>2 times per week) * Not sportman or regular exerciser (\>2 times per week or \>150 min per week) * No food allergy, especially shoot

Exclusion criteria

\- Current signs or symptoms of infection, i.e., fever, hyperpnea, dyspnea, and palpitations.

Design outcomes

Primary

MeasureTime frameDescription
Concentration of blood protein carbonylDay 0 and end of 12 weeksConcentration of blood protein carbonyl was measured in plasma in nmol/mg protein unit
Level of fat distributionDay 0 and end of 12 weeksLevel of fat distribution was measured by ratio of waist (centimeter) to hip (centimeter)
Level of body fatDay 0 and end of 12 weeksLevel of body fat was measured in percentage unit
Level of fat massDay 0 and end of 12 weeksLevel of fat mass was measured in kilogram unit
Concentration of blood glucoseDay 0 and end of 12 weeksConcentration of blood glucose was measured in serum in mmol/L unit
Concentration of blood insulinDay 0 and end of 12 weeksConcentration of blood insulin was measured in serum in uU/mL (microunit/milliliter) unit
Concentrations of blood lipidsDay 0 and end of 12 weeksConcentrations of total cholesterol, triglyceride, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol were measured in serum in mg/dL unit
Concentration of blood malondialdehydeDay 0 and end of 12 weeksConcentration of blood malondialdehyde was measured in plasma in uM (micromolar) unit

Secondary

MeasureTime frameDescription
Concentrations of blood glucose from oral glucose tolerance testAt 0 minute before glucose consumption and at 30, 60, 90, 120 minutes after glucose consumptionConcentrations of blood glucose were measured before and after glucose consumption at 75 g/100 ml in mg/dL unit

Countries

Thailand

Outcome results

None listed

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