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Assessment of vitamin D oral supplementationon on insulin resistance, visceral fat and adiponectin in women with polycystic ovary syndrome and hypovitaminosis D

Assessment of vitamin D oral supplementation on insulin resistance, visceral fat and adiponectin in women with polycystic ovary syndrome and hypovitaminosis D

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016101030248N1
Enrollment
44
Registered
2016-11-17
Start date
2016-05-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Polycystic Ovary Syndrome. Sclerocystic ovary syndrome Stein-Leventhal syndrome

Interventions

Intervention 1: Intervention: 8 vitamin D3 capsule 50000 IU during 2 month (1 capsule in the week after lunch). Intervention 2: Control: 8 placebo capsule(Paraffinedible) during 2 month (1 capsule in
Treatment - Drugs
Placebo
Intervention: 8 vitamin D3 capsule 50000 IU during 2 month (1 capsule in the week after lunch)
Control: 8 placebo capsule(Paraffinedible) during 2 month (1 capsule in the week after lunch)

Sponsors

Vice chancellor for research, Urmia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 38 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women with pcos according rotterdom criteria; Vitamin D deficiency ( x=<20 ng); OCPs consumer; Age between 20 to 38 Exclude criteria: Under 20 and over 38 years old; Neoplastic disorders; hepatic; renal; cardiovascular; malabsorptive and pregnancy; Those who consume vitamin D and taking antidiabetic drugs; People who follow a special diet pattern had specific physical activity

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Insulin resistance. Timepoint: before intervention-after intervention (2 month later). Method of measurement: insulin resistance: HOMA-IR, HOMA-B ,QUICKI.;Visceral fat. Timepoint: before intervention-after intervention(2 month later). Method of measurement: visceral fat :BIA(Inbody 770).;Adiponectin. Timepoint: before intervention-after intervention(2 month later). Method of measurement: Adiponectin.: serum adiponectin.

Secondary

MeasureTime frame
Sun exposure and physical activity. Timepoint: during intervention. Method of measurement: The questionnaire sunlight.;Diet. Timepoint: week 4-6-8. Method of measurement: 24-hour recalls.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Sakineh Nouri Saeidlou

Urmia University of Medical Sciences

saeedlou2003@yahoo.com; nourisaeidlou_s@umsu.ac.ir+98 44 3276 6825

Outcome results

None listed

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