Overview
The goal of this clinical trial is to learn if propolis administration works to change the level of Low Density Lipoprotein (LDL) and High Density Lipoprotein cholesterol (HDL) in diabetic type 2 patients.
The main questions it aims to answer are:
- Is giving 1 drops/ 10kg/ times, twice daily for 8 weeks will change the level of LDL and HDL level in diabetic type 2 patients compared to placebo? Researchers will compare propolis to a placebo (a look-alike substance that contains no drug) to see if propolis works to change LDL and HDL cholesterol level.
Participants will:
- Take propolis or a placebo, 2 times daily with given dose (1 drops/10 kg/times) every day for 2 months
- Visit the sub-district health centre once every 2 weeks for checkups
- Get their blood checked before and after intervention
Description
Subject allocation into groups will be made by third party to ensure masking/ blinding protocol.
Data that will be taken from participants :
- Private information
- Medication history (for type 2 Diabetes Mellitus)
- Food intake (calories, fats, carbohydrate, protein, and flavonoid intake)
- Physical activity status
Eligibility
Inclusion Criteria:
- Controlled Diabetes Mellitus type 2 with HbA1c <7.5%
- BMI 23-35 kg/m2
- On anti-cholesterol therapy
Exclusion Criteria:
- Using injection therapy (insulin or GLP-1 RA)
- History of bees product allergy
- Active smoker
- Consuming alcohol
- Altered liver (ALT>35 IU/L) and kidney (eGFR<90 mL/min) function
- Pregnant and breastfeeding women
- History of cardiovascular disease (heart attack, stroke)