Propolis effects on cholesterol levels in type 2 diabetes patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates whether propolis administration can alter Low Density Lipoprotein (LDL) and High Density Lipoprotein (HDL) cholesterol levels in patients with type 2 diabetes. Participants will receive either propolis or a placebo twice daily for eight weeks, with regular check-ups and blood tests to monitor changes in cholesterol levels. The study employs a randomized, double-blind design to ensure unbiased results. Data collected will include participants' medical history, dietary intake, and physical activity levels.

Why it matters

Who can join: the full rules

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)

Where it's running

• University of Indonesia Faculty of Biomedical Science
  Jakarta, Indonesia Recruiting

Study contacts

• Principal investigator: Dwirini R Gunarti, Biomed Science — Universitas Indonesia
• Study coordinator: Dwirini R Gunarti, Biomed Science
• Email: rinairet@gmail.com
• Phone: +62 8118382301

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.