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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Study Design

Type
Randomized Controlled Trial (RCT)
Population
70 Iranian married women aged 15-40 years with newly diagnosed PCOS
Methods
randomized placebo-controlled trial, 330 mg of S. officinalis extract or placebo daily for eight weeks
Blinding
Double-blind
Duration
eight weeks
Funding
Unclear

Background

Salvia.officinalis (S. officinalis), is recognized for its antihyperlipidemic, metabolism-regulating, and antioxidant properties in diabetic and hyperlipidemic disorders. This study examining its effects on lipid and oxidative stress (OS) markers in patients with Polycystic Ovary Syndrome (PCOS), thereby substantiating its role in managing metabolic disorders.

Methods

In this randomized placebo-controlled trial was performed in gynecology clinics affiliated to Iran University of Medical Sciences. Accordingly, 70 Iranian married women aged 15-40 years with newly diagnosed PCOS were included. They were randomized to receive either 330 mg of S. officinalis extract or placebo daily for eight weeks. The study outcomes included lipid profile and OS markers.

Results

The study found a significantly lower triglyceride levels and malondialdehyde after eight weeks of S. officinalis extract intake compared to placebo. Also, the mean change of triglyceride, high-density lipoprotein cholesterol, malondialdehyde, and total antioxidant capacity were statistically significant in intervention group.

Conclusion

The study demonstrates that S. officinalis extract can significantly reduce triglyceride levels and OS in patients with PCOS, suggesting its potential as an adjunctive natural therapy for managing metabolic and oxidative imbalances associated with this condition. While the extract did not significantly alter other lipid profile markers, the observed improvements highlight the therapeutic promise of S. officinalis. These findings support further investigation into the clinical applications S. officinalis for PCOS and its potential benefits for metabolic health.

Trial registration

IRCT201504146917N2 on 2015-10-03 (registered while recruiting).

Research Insights

  • the mean change of triglyceride, high-density lipoprotein cholesterol, malondialdehyde, and total antioxidant capacity were statistically significant in intervention group.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    330 mg daily
  • the mean change of triglyceride, high-density lipoprotein cholesterol, malondialdehyde, and total antioxidant capacity were statistically significant in intervention group.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    330 mg daily
  • While the extract did not significantly alter other lipid profile markers

    Effect
    Neutral
    Effect size
    Small
    Dose
    330 mg daily
  • The study found a significantly lower triglyceride levels and malondialdehyde after eight weeks of S. officinalis extract intake compared to placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    330 mg daily
  • While the extract did not significantly alter other lipid profile markers

    Effect
    Neutral
    Effect size
    Small
    Dose
    330 mg daily
  • The study found a significantly lower triglyceride levels and malondialdehyde after eight weeks of S. officinalis extract intake compared to placebo.

    Effect
    Beneficial
    Effect size
    Small
    Dose
    330 mg daily
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