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Astaxanthin in polycystic ovary syndrome

The effect of Astaxanthin on expression of ER stress pathway genes and apoptotic factors in granulosa cells of Polycystic ovary syndrome patient candidate for Assisted reproductive technology: RCT(Triple-blind)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201029049183N1
Enrollment
60
Registered
2020-11-27
Start date
2021-01-15
Completion date
Unknown
Last updated
2021-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovarian Syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group: Astaxanthin consumption. In this group, patients take 12 mg of astaxanthin daily ( in 2 capsules of 6mg twice in the morning and at night) for 60 days. Their routin

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Hyperandrogenism Oligo/anovulation (ovulationabnormality) Polycystic ovaries on ultrasound

Exclusion criteria

Exclusion criteria: Pregnancy Adrenal hyperplasia Androgen-secretingtumors Hyperprolactinemia Thyroid dysfunction Diabetes mellitus or glucose tolerance Male infertility factors

Design outcomes

Primary

MeasureTime frame
ER stress and apoptotic factor. Timepoint: 60 days after the beginning of the intervention. Method of measurement: real time pcr, western blot.;High density lipoprotein cholesterol (HDL). Timepoint: Before and 60 days after the intervention. Method of measurement: Enzyme kit.;Glutathione peroxidase 3 (GPX3) gene. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Real time pcr.;Pentraxin 3 (PTX3) gene. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Real time pcr.;Runt-related transcription factor 2 (RUNX2) gene. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Real time pcr.;Phosphoglycerate kinase 1 (PGK1) gene. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Real time pcr.;Regulator of G-protein signaling2(RGS2)gene. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Real time pcr.

Secondary

MeasureTime frame
Number and quality of oocytes. Timepoint: 60 days after the beginning of the intervention. Method of measurement: Counting,light microscope.;Number and quality of embryos. Timepoint: 60-63 days after the beginning of the intervention. Method of measurement: Counting,light microscope.;Chemical pregnancy. Timepoint: 14 days after embryo transfer. Method of measurement: beta-hCG blood test.;Fasting insulin. Timepoint: Before and 60 days after the intervention. Method of measurement: Elisa kit.;Total cholesterol. Timepoint: Before and 60 days after the intervention. Method of measurement: Enzyme kit.;Triglycerides. Timepoint: Before and 60 days after the intervention. Method of measurement: Enzyme kit.;Low density lipoprotein (LDL). Timepoint: Before and 60 days after the intervention. Method of measurement: Enzyme kit.;Fasting blood sugar. Timepoint: Before and 60 days after the intervention. Method of measurement: Enzyme kit.;Malondialdehyde (MDA). Timepoint: Before and 60 days after the intervention. Method of measurement: Spectrophotometry.;Total antioxidant capacity (TAC). Timepoint: Before and 60 days after the intervention. Method of measurement: Spectrophotometry.;Superoxide dismutase (SOD). Timepoint: Before and 60 days after the intervention. Method of measurement: Spectrophotometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTehran University of Medical Sciences

Tehran University of Medical Sciences

amidifardin@yahoo.com+98 21 6405 3411

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026