Ovarian Cysts Clinical Trials

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The Effectiveness of Astaxanthin Supplementation on the Clinical Symptoms and Cardio-metabolic Profile in Women with Polycystic Ovary Syndrome: a Protocol for a Randomized Double-blinded, Placebo-controlled Parallel-group Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

Background: This trial aims to investigate the effect of 12 weeks of 10 mg/day astaxanthin (ASX) administration compared with the control group on insulin sensitivity, lipid profile, circulating MDA levels, severity of hirsutism, and depression in women with Polycystic Ovary Syndrome (PCOS).

Methods: This manuscript will outline the design, methodology, and potential clinical implications of ASX supplementation in eligible women with PCOS and a body mass index of 25-35 kg/m2, who are referred to the gynecologist clinic in Isfahan, Iran, during 2024-2025. Discussion: This study is one of the first attempts to assess the clinical efficacy of astaxanthin as an auxiliary treatment in PCOS patients, and will provide more evidence in this area. Trial registration number: Iran Clinical Trials (IRCT) website. (IRCT20231001059573N1)

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: f
View:

• Age 18 - 45 years

• Clinical diagnosis of polycystic ovary syndrome

• Have a body mass index of 25-35 kg/m 2

• Absence of pregnancy and breastfeeding

• No intake of medicine

• Not willing to get pregnant during the study

• No presence of chronic inflammatory diseases or other endocrine disorders

• No current treatments except metformin

• No intake of dietary supplements within at last 2 previous months

Locations
Other Locations
Islamic Republic of Iran
Isfahan university of medical sciences
RECRUITING
Isfahan
Contact Information
Primary
Nafiseh Shokri-Mashhadi, Dr.
miladnacri@gmail.com
+989134312432
Backup
Milad Nasiri Jounaghani
miladnasiri.j@gmail.com
+989338033133
Time Frame
Start Date: 2024-07-22
Estimated Completion Date: 2025-07-22
Participants
Target number of participants: 44
Treatments
Experimental: Drug
receiving ASX supplements
Placebo_comparator: control
receiving placebo
Sponsors
Leads: Isfahan University of Medical Sciences

This content was sourced from clinicaltrials.gov