Clinical Trials Directory

Trials / Unknown

UnknownNCT05770297

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

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Indonesia University · Academic / Other
Sex
Female
Age
20 Years – 49 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPropolisintervention will use propolis extract (liquid-based) with 1 drop/10kgBW/times, 2 times in a day for 12 weeks. propolis will be given to intervention group
OTHERplacebointervention will use placebo with 1 drop/10kgBW/times, 2 times in a day for 12 weeks. propolis will be given control group

Timeline

Start date
2022-07-12
Primary completion
2023-06-22
Completion
2023-07-11
First posted
2023-03-15
Last updated
2023-06-06

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT05770297. Inclusion in this directory is not an endorsement.