CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 116 enrolled / 116 target
Drug / intervention
Herbal Formulation +2 moredrug
Likely dose
Metformin 750 mg and herbal formulation 500 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07603505
NCT07603505Phase 1CompletedOn Track (7.9/mo)Completion was 1mo ago

Effect of Nepeta Adenophyta Hedge Extract and Its Fractions on Polycystic Ovarian Syndrome (PCOS)

Jinnah Sindh Medical University·interventional·Posted May 22, 2026·Updated Jun 22, 2026

In Brief

A Phase 1 clinical trial evaluating Herbal Formulation, Metformin XR, and 1 other intervention for Polycystic Ovarian Syndrome (PCOS) and 2 related conditions. Completed, enrolled 116 participants across 1 site.

Detailed Summary

Polycystic Ovarian Syndrome (PCOS) is a multifaceted endocrine metabolic condition impacting about 5-10% of women throughout their reproductive lifespan. It is influenced by neuroendocrine dysfunction, insulin resistance, chronic low-grade inflammation, and ovarian oxidative stress. Existing medications, including metformin, clomiphene citrate, and anti-androgens, provide only limited advantages and are frequently restricted by side effects such as gastrointestinal intolerance, teratogenic risks, and weight gain. NAE (family Lamiaceae) is a fragrant perennial herb indigenous to the Himalayan and sub-Himalayan areas of Pakistan and Afghanistan. Phytochemical profiling of this plant has revealed high concentrations of flavonoids (luteolin, apigenin, quercetin), phenolic acids (rosmarinic and caffeic acid), terpenoids (nepetalactones), and glycosides. In a preclinical study lasting 30 days that involved Letrozole induced PCOS in Albino Wistar rats, the oral delivery of crude extract (350 and 500 mg/kg) and its methanol/butanol fractions (64 mg/kg; 12.5mg/kg) significantly restored estrous cyclicity, decreased serum LH and testosterone levels, normalized the LH/FSH ratio, enhanced insulin sensitivity (reduced HOMA IR), corrected dyslipidaemia, and reversed ovarian histopathological alterations. Molecular analysis by qRT PCR showed upregulation of IL 4 and downregulation of AR, CYP-17, TLR4, TNF α, and NF κB. Based on this multi targeted preclinical efficacy and a favourable safety profile, this clinical trial will assess the safety and effectiveness of a standardised NAE in women with PCOS, compared to metformin and combination therapy over 4 months.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesPakistan
Collaborators--

Timeline

Phase 1CompletedFinished
2026
First PostedMay 22, 2026
Enrollment StartApr 10, 2025
Primary CompletionMay 30, 2026
Study CompletionJun 15, 2026
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 1 month ago

Arms & Interventions

NAE treated groupexperimental

NAE 500 mg twice daily for 4 months in PCOS patients

Drug: Herbal Formulation
Metformin XR treated groupactive_comparator

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

Drug: Metformin XR
Adjunct Groupexperimental

NAE 500 mg and Metformin XR 750 mg twice daily for 4 months in PCOS patients

Drug: Metformin 750 mg and herbal formulation 500 mg

Interventions

Herbal Formulationdrug

NAE 500 mg twice daily for 4 months in PCOS patients

Metformin XRdrug

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

Metformin 750 mg and herbal formulation 500 mgdrug

NAE 500 mg and Metformin XR 750 mg twice daily for 4 months in PCOS patients