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Effect of Propolis Administration for Dysmenorrhea in Endometriosis Patient With Levonorgestrel Implant Therapy

Endometriosis Clinical Trial

Official title:
Effect of Propolis Administration as Levonorgestrel (LNG) Implant Adjuvant for Dysmenorrhea in Endometriosis: Focus on Clinical Improvement, Oxidative Stress Biomarkers and Inflammation

Clinical Trial Summary

The goal of this clinical trial is to investigate the effect of propolis administration on dysmenorrhea in endometriosis patient. the main questions it aims to answer are: - Does the propolis administration reduce symptoms of dysmenorrhea in endometriosis? - Does the propolis administration reduce the amount of oxidative stress biomarkers in endometriosis? - Does the propolis administration reduce the amount of Inflammatory biomarkers in endometriosis? Participants will be given an intervention in the form of propolis at a dose of 1 drop per 10 kilogram of body weight per administration, twice a day. there will be a control group that will be given an intervention in the form of a placebo containing 70% caramel alcohol dye solution.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05770297
Study type Interventional
Source Indonesia University
Contact
Status Recruiting
Phase N/A
Start date July 12, 2022
Completion date July 11, 2023
View Details
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