The Effect of Propolis Administration on Low Density Lipoprotein and High Density Lipoprotein in Diabetic Type 2 Patients in Central Jakarta

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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

Eligibility
Participation Requirements
Sex: All
Minimum Age: 35
Maximum Age: 59
Healthy Volunteers: f
View:

• Controlled Diabetes Mellitus type 2 with HbA1c \<7.5%

• BMI 23-35 kg/m2

• On anti-cholesterol therapy

Locations
Other Locations
Indonesia
University of Indonesia Faculty of Biomedical Science
RECRUITING
Jakarta
Contact Information
Primary
Dwirini R Gunarti, Biomed Science
rinairet@gmail.com
+62 8118382301
Backup
Wiryani Sentosa, MD
wiryani@ymail.com
+62 81210977847
Time Frame
Start Date: 2025-03-18
Estimated Completion Date: 2025-07-31
Participants
Target number of participants: 64
Treatments
Experimental: Intervention group
This group will receive the intervention, which in this study is propolis with dose given 1 drop/kg/time given, 2 times daily, for 8 weeks (2 months)
Placebo_comparator: Control group
This group will receive placebo (a look-alike substance that contains no drug) with dose given 1 drop/kg/time given, 2 times daily, for 8 weeks (2 months)
Related Therapeutic Areas
Sponsors
Leads: Indonesia University

This content was sourced from clinicaltrials.gov

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