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The effect of zinc sulfate and folic acid on endocrine indices, CRP and lipid profile in women with polycystic ovary syndrome

The effect of zinc sulfate and folic acid on endocrine indices, CRP and lipid profile in women with polycystic ovary syndrome in 2017-18.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200610047715N1
Enrollment
50
Registered
2020-12-27
Start date
2017-12-01
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Polycystic ovary syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group: The first group received 220 mg of zinc sulfate (containing 50 mg of zinc) daily for 8 weeks. Intervention 2: Intervention group: the second group received 5 mg of

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Oligoovulation or / and anovulation Clinical symptoms (Ferriman-Gallwey score=6 or Acne or Seborrhoeic) or biochemical hyperandrogenism Evidence of polycystic ovaries on ultrasound

Exclusion criteria

Exclusion criteria: Hyperprolactinoma Thyroid disease Cardiovascular diseases Kidney-liver and neoplastic diseases Type 2 diabetes Pregnancy or breastfeeding Absorption disorders Use of drugs such as anti-diabetic drugs, anti-obesity drugs, diuretics, OCP, steroid and hormonal drugs (at least 3-6 months) and drugs that interfere with folic acid (perimetamine, aspirin, carbamazepine, chloramphenicol, chlorothiazide, conjugated estrogens, forge , Hydrochlorothiazide, Methotrexate, Phenytoin, Phenobarbital, Sulfamethoxazole, Salicylate)

Design outcomes

Primary

MeasureTime frame
FBS. Timepoint: 8 weeks after taking the drug. Method of measurement: BT4500.;Dehydroepiandrosterone sulfate. Timepoint: 8 weeks after taking the drug. Method of measurement: ELISA reader.;Testosterone. Timepoint: 8 weeks after taking the drug. Method of measurement: ELISA reader.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Shafipour

Rafsanjan University of Medical Sciences

mr.shafiepour@gmail.com+98 34 3428 0000

Outcome results

None listed

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