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CompletedNCT04013490Updated Feb 21, 2020

Safety Evaluation and Effect of Food Supplement Containing Dietary Fiber From Cassava on the Alterations of Physiological Parameters in Overweight Female Volunteers

A Phase 1 interventional study of Cassava dietary fiber capsule in Overweight, sponsored by Khon Kaen University. Completed at 1 site in Thailand. Open to female participants aged 35 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-02-21.

Sponsored by Khon Kaen University · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Feb 2019, registered Jun 2019).
Phase
Phase 1
Study type
Interventional
Enrollment
75
Allocation
Randomized
Ages
35 Years to 60 Years
Sex
Female
01

Study summary

This study is set up to determine the consumption safety and the effect of a food supplement containing dietary fiber from cassava on the alterations of physiological parameters including fasting blood sugar, HbA1c, insulin resistance, lipid profiles, atherogenic index, blood pressure and gut microbes in overweight female volunteers.

Read the detailed description

Cassava is one of the important industrial crops in Thailand. The leftover fiber of cassava is still valuable and can be used as a dietary fiber. The previous study demonstrated that dietary fiber containing cassava fiber was safe for consumption without any contamination of the cyanide and heavy metals. Moreover, the microbial contaminations were within the safety range. The toxicity study revealed that the LD50 of the cassava dietary fiber was more than 5 g/kg body weight (BW) and NOAEL was 3 g/kg BW. The NOAEL was used to calculate the human equivalent dose for determining the effect of cassava dietary fiber in a clinical study.

Cassava dietary fiber consists of water-insoluble fiber such as cellulose more than 50%. The previous study showed that insoluble fiber decreased the risk of type 2 diabetes and increased insulin release. Moreover, a high fiber diet also decreased the fasting glucose and HbA1C in type 2 diabetes volunteer. In addition, the effect of dietary fiber on the reduction of cholesterol was also reported. The previous study reported that the cassava dietary fiber could decrease the total cholesterol, triglyceride but increase high-density lipoprotein in a dyslipidemia rat model. Therefore, the cassava fiber might be the potential food supplement for the control of blood sugar and lipid profiles in human. However, less scientific data support the effect of cassava dietary fiber in human.

02

Conditions studied

  • Overweight

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Keywords

  • physiological parameters
  • consumption safety
  • cassava
  • food supplement
  • overweight female
03

In context

Overweight

3,670 studies on the registry are indexed under Overweight; 849 are open to participants now.

This study's enrollment of 75 is close to the median of 73 across 3,175 interventional studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

Khon Kaen University is the lead sponsor of 160 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy women age between 35-60 years old
  • BMI 23-29.99
  • Blood pressure \<140/90 mmHg
  • Fasting plasma glucose \< 100 mg/dL

Exclusion criteria

Exclusion Criteria:

  • Presence of any chronic diseases
  • Alcohol addict or consume more than 2 units/day
  • Smoking more than 10 cigarettes per day
  • Medication or herbal medicine usage within 1 month prior to the study
  • Use any medication or food supplement which affect to outcomes
  • Pregnant or breastfeeding women
  • Athlete
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
75 participants (actual)

Study arms

  • Placebo comparator
    Placebo capsule

    Subject receive the Placebo product for 4 weeks.

    Dietary Supplement: Cassava dietary fiber capsule

  • Active comparator
    Cassava dietary fiber capsule 1.5 g/day

    Subjects receive Cassava dietary fiber capsule at the dose of 1.5 g/day for 4 weeks.

    Dietary Supplement: Cassava dietary fiber capsule

  • Active comparator
    Cassava dietary fiber capsule 3 g/day

    Subjects receive Cassava dietary fiber capsule at the dose of 3 g/day for 4 weeks.

    Dietary Supplement: Cassava dietary fiber capsule

Interventions

  • Dietary supplementCassava dietary fiber capsule

    Cassava dietary fiber capsule or placebo will be consumed once daily at the recommended doses of each group.

06

What researchers measure

Primary outcomes

  1. The fasting blood sugar level

    The previous study reported that high dietary fiber could decrease the fasting blood sugar in type 2 diabetes patient. The overweight female volunteer receive food supplement containing dietary fiber from Cassava should show the lower level of fasting blood sugar than the placebo-treated group after 4 weeks of intervention.

    Time frame: Baseline and 4 weeks of intervention

  2. The atherogenic index

    The atherogenic index is an index composed of triglycerides and high-density lipoprotein cholesterol. It has been used to quantify blood lipid levels and commonly used as an optimal indicator of dyslipidemia and associated diseases. The food supplement containing dietary fiber from Cassava might be able to decrease the atherogenic index in overweight female volunteer. The overweight female volunteer receive food supplement containing dietary fiber from Cassava should show the lower number of the atherogenic index than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

Secondary outcomes

  1. hemoglobin A1c concentration

    A hemoglobin A1c (HbA1c) test measures the amount of blood sugar (glucose) attached to hemoglobin. This result shows the average amount of glucose attached to hemoglobin has been over the past three months. The previous study reported that high dietary fiber could decrease the HbA1C in type 2 diabetes patient. The food supplement containing dietary fiber from Cassava might be able to decrease the HbA1C in overweight female volunteer. The overweight female volunteer receive food supplement containing dietary fiber from Cassava should show the lower HbA1C level than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  2. Homeostasis model assessment-insulin resistance (HOMA-IR)

    HOMA-IR was computed with the formula: fasting plasma glucose (mmol/l) multiplied fasting serum insulin (mU/l) divided by 22.5. Low HOMA-IR values indicate high insulin sensitivity, whereas high HOMA-IR values indicate low insulin sensitivity (insulin resistance). The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show the lower HOMA-IR than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  3. Low-density lipoprotein (LDL) concentration

    LDL is considered bad cholesterol and a leading cause of atherosclerosis formation. The food supplement containing dietary fiber from Cassava might be able to decrease the LDL level in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show the lower LDL concentration than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  4. High-density lipoprotein (HDL) concentration

    HDL is considered as good cholesterol and believed that it acts as a scavenger and carrying of LDL from the arteries back to the liver. The food supplement containing dietary fiber from Cassava might be able to increase the LDL level in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show a higher HDL concentration than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  5. Triglyceride (TG) concentration

    TG is one type of fat in the blood which converted from the excess energy from the diet. A high triglyceride level combined with high LDL (bad) cholesterol or low HDL (good) cholesterol is linked with fatty buildups within the artery walls, which increases the risk of heart attack and stroke in an overweight person. The food supplement containing dietary fiber from Cassava might be able to decrease the LDL level in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show the lower TG concentration than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  6. Cholesterol concentration

    The high level of cholesterol is a cause of atherosclerosis in the blood vessel. The food supplement containing dietary fiber from Cassava might be able to decrease the cholesterol level in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show the lower cholesterol concentration than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  7. Body mass index (BMI)

    The food supplement containing dietary fiber from Cassava might be able to decrease the BMI in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show the lower BMI than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  8. Gut microbes

    It has been reported that the dysbiosis can cause the alteration of glucose metabolism, lipid metabolism, and dyslipidemia. Moreover, the high fiber diet causes the elevation of good bacteria in the gut and exert many effects. The food supplement containing dietary fiber from Cassava might be able to increase the good gut microbes in overweight female volunteer. The overweight female volunteers receive food supplement containing dietary fiber from Cassava should show higher gut microbes than the placebo-treated group after 4 weeks of intervention.

    Time frame: 4 weeks of intervention

  9. The consumption safety of food supplement containing dietary fiber from Cassava using Systolic and Diastolic Blood pressure

    If the supplement containing dietary fiber from Cassava is safe, the blood pressure should be within the normal range.

    Time frame: 4 weeks of intervention

  10. The consumption safety of food supplement containing dietary fiber from Cassava using the electrocardiogram pattern and QT interval data

    If the supplement containing dietary fiber from Cassava is safe, the EKG pattern and the QT interval should be within the normal range.

    Time frame: 4 weeks of intervention

  11. Consumption safety of food supplement containing dietary fiber from Cassava using blood chemistry

    The blood chemistry values including renal function test, liver function test, and electrolytes will be determined and the data will be expressed as the number of subjects presented with abnormal blood chemistry value.

    Time frame: 4 weeks of intervention

  12. Consumption safety of food supplement containing dietary fiber from Cassava using hematolgical values.

    The hematological values including red blood cell, white blood cell, hematocrit, and platelet will be determined and the data will be expressed as a number of subjects presented with abnormal hematological value.

    Time frame: 4 weeks of intervention

07

Study locations

1 site
  • Jitanaporn Wattanathorn
    Khon Kaen, 40002, Thailand
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04013490
Lead sponsor
Khon Kaen University
Responsible party
Jintanaporn Wattanathorn (Associated Professor, Khon Kaen University) — Principal investigator
First posted
Jul 9, 2019
Start date
Feb 27, 2019
Primary completion
Jul 31, 2019
Completion
Aug 31, 2019
Last update
Feb 21, 2020

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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