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Study on Narie PCOS to evaluate itâ??s efficacy in the management of Poly Cystic Ovarian Syndrome

A Clinical study to evaluate the efficacy of Narie PCOS in the management of Poly Cystic Ovarian Syndrome (Aarthava Akshaya) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091372
Enrollment
50
Registered
2025-07-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: E282- Polycystic ovarian syndrome

Interventions

None listed

Sponsors

Zeroharm Science Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient diagnosed with PCOS 2. Patient with chief complain of Irregular menses / scanty menses 3. Patients suffer infertility due to PCOS. 4.Subjects willing to follow the procedures as per the study protocol and voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: Pregnant or Lactating women Congenital anomalies in female genital tract or Congenital adrenal hyperplasia Malignant diseased patients and cytotoxic patients.

Design outcomes

Primary

MeasureTime frame
Assessment Criteria (Based on Grade & Score) 1. Duration of bleeding 2. Irregular menstruation 3. Amount of bleeding and quantity of menstrual blood 4. Pain during menstrual period Timepoint: 12 weeks—

Secondary

MeasureTime frame
1. Haematological- CBC, ESR, Blood group, Urine (R/M), LH,FSH Follicular study- A serial vaginal or abdominal sono graphy was done from 10th day of menstrual cycle,till after ovulation.Timepoint: 12 weeks—

Countries

India

Contacts

Public ContactDr Dipak Kumar Goswami

Government Ayurvedic College and Hospital

dr.dkgoswami@gmail.com9435400876

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026