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The Effect of Symbiotic Beverage Consumption on Lipid Profile (SYMBIONIC)

P

Politeknik Kesehatan Kemenkes Padang

Status

Active, not recruiting

Conditions

Lipid Profile
Body Mass Index
Fasting Blood Sugar Above Normal

Treatments

Dietary Supplement: SYMBIONIC
Behavioral: Dietary advice

Study type

Interventional

Funder types

Other

Identifiers

NCT06893991
PoliteknikKKP

Details and patient eligibility

About

The goal of this clinical trial is to evaluate whether the synbiotic beverage "Daygurt" can improve lipid profiles, blood sugar levels, blood pressure, and body weight in individuals diagnosed with dyslipidemia. The main questions it aims to answer are:

Does "Daygurt" significantly reduce total cholesterol and LDL levels compared to nutrition counseling alone? Does "Daygurt" increase HDL levels and reduce triglycerides more effectively than nutrition counseling? Does "Daygurt" lead to greater improvements in fasting blood sugar, blood pressure, and body weight compared to nutrition counseling?

The intervention group (receiving "Daygurt" plus nutrition counseling) will be compared to the comparison group (receiving nutrition counseling without "Daygurt") to see if "Daygurt" provides additional benefits beyond standard dietary advice.

Participants will be divided into 2 groups:

Intervention group: Consume "Daygurt" daily for 8 weeks. Comparison group: Receive nutrition counseling sessions focused on managing dyslipidemia but will not consume "Daygurt."

Both groups will undergo health parameter measurements before and after the intervention, including:

Total cholesterol, LDL, HDL, and triglyceride levels. Fasting blood sugar. Blood pressure. Body mass index (BMI).

Enrollment

60 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cholesterol total above 200 mg/dl, or LDL Cholesterol above 100, or BMI above 25 kg/m2
  • Agree to study protocols

Exclusion criteria

  • Has Allergic to dairy product
  • Having any drug lowering cholesterol

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Intervention Group
Experimental group
Description:
Consuming 100 ml Symbiotic beverages every day for 6 weeks plus dietary advice to overcome dyslipidemia
Treatment:
Behavioral: Dietary advice
Dietary Supplement: SYMBIONIC
Comparison group
Active Comparator group
Description:
Receiving standard dietary advice to overcome dyslipidemia, but without drinking symbiotic beverage
Treatment:
Behavioral: Dietary advice

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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