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Completed

NCT Number: NCT07399535

Clinical Investigation of Herbal Formulation and Its Efficacy in Polycystic Ovarian Syndrome

Polycystic Ovarian Syndrome (PCO) is a metabolic disorder that afflicts the women of childbearing age. An approximate of 5-10% women are the victim of this disorder. PCOS is a leading cause of infertility in females these days and is characterized by Hyperandrogenism, Chronic Anovulation, Impaired fertility, obesity, Hirsutism, Acne, Obesity, Metabolic disturbances (dyslipidemias, Hyperinsulinemia, insulin resistance, and type- 2 diabetes), and Endometrial Hyperplasia. This study will test a combination of herbal medications (Melats P) in women with PCOS to determine which works best to overcome infertility.

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Key information

About this study

Polycystic Ovarian Syndrome is a point of concern these days in female population around the world.The patients feel psychological and mentally unhealthy. PCO effects around 6- 14% of women worldwide. PCOS is characterized by hormonal dis-regulation and hyperinsulinemia. Improvements in sex hormones and insulin sensitivity in PCOS women, either through lifestyle changes or through pharmaceutical intervention, have consistently resulted in a marked improvement in the reproductive and metabolic abnormalities in PCOS Commonly prescribed treatment for PCOS include oral contraceptives (OCPs), metformin, pioglitazone, estrogen, GnRH agonist, myo-inositol, letrozole and clomiphene citrate. Despite their effectiveness in symptom relief and ovulation induction, these treatments are associated with adverse effects including weight gain, cardiac issues, lactic acidosis, dysmenorrhea, and abdominal discomfort (Hussain et al., 2022). Given the limitations of conventional drugs, Herbal therapies are gaining attention for their multi-targeted ability to restore natural hormonal balance, improve ovulation and offer symptom relief with minimal side effects (Hussain et al., 2022). In this context, the present study is designed to explore the therapeutic benefits of a novel polyherbal formulation that includes Momordica charantia L., Linum usitatissimum, Symplocos racemose bark, Allium cepa L., Tribulus terrestris, and eggshell. These ingredients were selected based on their various pharmacological properties that are relevant to the pathophysiology of PCOS. This study will evaluate the safety and effectiveness of Melats P in achieving a successful menstruation regulation in PCOS women.We will recruit 3 groups , First group with conventional treatment (Metformin ) , Second with Alternative medicine having a herbal Formulation ( Melats P) and Third group patients will receive both Conventional (Metformin) and Herbal Formulationn (Melats P).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female subjects of reproductive age (18-40 years).
  • Subjects with a diagnosis of polycystic ovary syndrome (PCOS) confirmed by clinician diagnostic criteria.
  • Subjects with insulin resistance defined as HOMA-IR > 2.00.

Exclusion criteria

  • Pregnant or lactating women.
  • Subjects with known Cushing's syndrome.
  • Subjects with late-onset congenital adrenal hyperplasia.
  • Subjects with androgen-secreting tumors.
  • Subjects with uncontrolled thyroid disease.
  • Subjects with hyperprolactinemia.
  • Subjects with diabetes mellitus.
  • Subjects with uncontrolled hypertension.
  • Subjects with other cardiovascular diseases.
  • Subjects with acute or chronic infections.
  • Subjects with any known malignancy.
  • Subjects with impaired renal function (serum creatinine > 1.5 × ULN).
  • Subjects with impaired liver function (serum ALT ≥ 2.5 × ULN).

Treatment and study plan

Herbal Formulation

Drug

Herbal Formulation 500mg twice daily for 4 months in PCOS patients

Other names: Melats P

Metformin XR

Drug

Metformin XR 750mg twice daily for 4 months in PCOS patients

Other names: Glucophage

Metformin 750 mg and herbal formulation 500 mg

Drug

Herbal formulation and Metformin twice daily for 4 months in PCOS patients

Primary outcomes

  1. Regulation of Menstrual Cycle

    Time frame: Baseline to 4 months

    Improvement and restoration of regular ovulatory menstrual cycles ( cycle length 21-35 days) after 4 months of treatment, assessed through menstrual history and ultrasonographic confirmation of ovulation. Ovulation confirmed by transvaginal ultrasonography, defined by the presence of a dominant follicle followed by follicular rupture during the treatment period.

Secondary outcomes

  1. Serum Follicle-Stimulating Hormone (FSH) Levels

    Time frame: Baseline and after 4 months

    Change in serum follicle-stimulating hormone (FSH) concentration measured using standard laboratory assays. Unit of Measure: mIU/mL, Normal Range: Women (Follicular Phase): 3.5 - 12.5 , Women (Ovulation Phase): 4.7 - 21.5, Women (Luteal Phase): 1.7 - 7.7

  2. Serum Luteinizing Hormone (LH) Levels

    Time frame: Baseline and after 4 months

    Change in serum luteinizing hormone (LH) concentration measured using standard laboratory assays. Unit of Measure: mIU/mL, Normal Range: Women (Follicular Phase): 1.9 - 9.2, Women (Ovulation Phase): 6.1 - 49.1, Women (Luteal Phase): 1.3 - 10.8

  3. Serum Testosterone Levels

    Time frame: Baseline and after 4 months

    Change in serum testosterone levels measured using standard laboratory assays. Unit of Measure: ng/mL, Normal Range: 18-49 years: 0.084-0.481

  4. Glycated Hemoglobin (HbA1c) Level

    Time frame: Baseline and after 4 months

    Change in glycated hemoglobin (HbA1c) percentage measured using standardized laboratory methods. Unit of Measure: %, Normal Range: Normal <5.6%, Prediabetes: 5.7% - 6.4%, Diabetes: 6.5% or higher

  5. Fasting Serum Insulin Concentration

    Time frame: Baseline and after 4 months

    Change in fasting serum insulin concentration measured using standard laboratory assays. Unit of Measure: µIU/mL, Normal Range: 2 to 25

  6. HOMA-IR

    Time frame: Before and after 4 months

    HOMA-IR will be calculated before and immediately after 90-day treatment. HOMA-IR is calculated using the following equation: HOMA-IR = fasting plasma glucose in mmol/L×fasting insulin in μU/ml/22.5.

  7. Body Weight

    Time frame: Baseline and after 4 months

    Change in body weight measured using a calibrated weighing scale. Unit of Measure:

    kg

Other outcomes

  1. Assessment of quality of life via Polycystic Ovary Syndrome Quality of Life scale (PCOSQOL)

    Time frame: Before and after 4 months

    The Polycystic Ovary Syndrome Quality of Life Scale (PCOSQOL) is a disease-specific questionnaire used to assess the impact of polycystic ovary syndrome on quality of life. It evaluates five domains: Emotions (8 items), Body Hair (5 items), Weight (5 items), Infertility Problems (4 items), and Menstrual Problems (4 items). Cronbach's alpha were above 0.7 when the PCOSQL was validated (Jones et al., 2004). It has 26 items and uses a 7-point Likert-type scale.

    Scale Range:

    Minimum value: 1 Maximum value: 7

    Lower scores indicate decreased quality of life, while higher scores indicate improved quality of life.

Sponsors and collaborators

Lead sponsor

Jinnah Postgraduate Medical Centre

Other Gov

Registry information

Acronym: PCOS

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 10, 2026
Registry last updated
Jun 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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