MedPath

Effect of Quercetin Supplementation on Endometriosis Outcomes

Not Applicable
Recruiting
Conditions
Endometriosis
Interventions
Other: Placebo
Dietary Supplement: Quercetin
Registration Number
NCT05983224
Lead Sponsor
National Nutrition and Food Technology Institute
Brief Summary

Quercetin is a polyphenol compound that possesses anti-inflammatory properties and can be found in various food sources like apples, berries, cabbage, and onions. In Park et al.'s study, it was discovered that quercetin led to a significant decrease in the proliferation of endometriosis cells. Furthermore, quercetin also triggered apoptosis in endometriosis cells in vitro and reduced the size of endometriosis lesions in vivo. Nevertheless, as of now, there have been no studies conducted in Iran or worldwide that explore the effects of quercetin supplementation on individuals with endometriosis. Hence, the aim of this study is to investigate the impact of quercetin supplementation on factors such as glycemic status, lipid profile, oxidative stress, inflammation, growth factors, adiponectin, sex hormones, and anthropometric indicators in women suffering from endometriosis.

Detailed Description

The participants in the study were randomly assigned to two groups: the intervention group and the control group. The intervention group will receive two 500 mg quercetin tablets daily, after breakfast and lunch, for twelve weeks. On the other hand, the control group will be given a placebo. Blood samples will be collected before and after the intervention to measure changes in blood lipid profile, fasting blood sugar, sex hormones (testosterone, estrogen, progesterone), TNFα, IL-6, adiponectin, IGF1, HbA1C, SHBG, FSH, LH, and plasma total antioxidant capacity.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
50
Inclusion Criteria
  • Willing to cooperate and complete the informed consent form.
  • Diagnosed endometriosis using laparoscopy and histopathological tests.
  • In the age group of 18 to 40 years.
  • Having a regular menstrual cycle.
  • Having a body mass index between 18.5 and 30.
Exclusion Criteria
  • Using hormonal medications or intrauterine treatments for a minimum of three months prior to collecting a sample.
  • Having immune system disorders, persistent infections, diabetes, or any conditions like polyps and fibroids within the uterine cavity.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboThe Placebogroup will receive Placebo tablets daily, after breakfast and lunch, for twelve weeks.
QuercetinQuercetinThe intervention group will receive two 500 mg quercetin tablets daily, after breakfast and lunch, for twelve weeks.
Primary Outcome Measures
NameTimeMethod
Mean serum TNF-alpha concentration12 weeks

Human Tumor Necrosis Factor Αlpha, TNF-A ELISA Kit

Mean serum IL-6 concentration12 weeks

Human Interleukin 6, IL-6 ELISA Kit

Secondary Outcome Measures
NameTimeMethod
Mean Serum Testosterone concentration12 weeks

The Testosterone ELISA Kits

Mean Serum Estrogen concentration12 weeks

The Total Estrogens ELISA Assay Kit

Mean Serum FSH concentration12 weeks

FSH (Human) ELISA Kit

Mean HbA1C Serum12 weeks

Human Hemoglobin A1c (HbA1c) Assay Kit

Mean Serum Adiponectin concentration12 weeks

Adiponectin Human ELISA Kit

Mean Serum Progesterone concentration12 weeks

The Progesterone Enzyme Immunoassay Kit

Mean Serum FBS concentration12 weeks

Glucose Test Kit

Mean Serum SHBG concentration12 weeks

liquid chromatography-tandem mass spectrometry

Mean plasma total antioxidant capacity concentration12 weeks

Total Antioxidant Capacity ELISA Kit

Mean Serum IGF1 concentration12 weeks

IGF-1 ELISA Assay Kit

Mean Serum LH concentration12 weeks

LH (Human) ELISA Kit

Trial Locations

Locations (1)

National Nutrition and Food Technology Research Institute

🇮🇷

Tehran, Iran, Islamic Republic of

© Copyright 2025. All Rights Reserved by MedPath