Comparative clinical trial to evaluate the efficacy of shatapushpa churna and shatapushpa taila nasya in artava dushti w.s.r. to poly cystic ovarian syndrome.

Randomized comparative clinical trial to evaluate the efficacy of shatapushpa churna along with shatapushpa taila nasya in artava dushti w.s.r. to poly cystic ovarian syndrome (PCOS) - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/100757

Enrollment

Registered

2026-01-09

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Eligibility

Inclusion criteria

Inclusion criteria: 1. If Patient willing to give informed consent to be included. 2. Female patient of age group between 18 - 40 years (both married and unmarried). 3. ASRM or ESHRM (Rotterdam) criteria Affected patient must follow two out of three criteria (1) Anovulation, (2) Hyperandrogenism (clinical/biochemical), (3) Polycystic Ovaries (confirmed by USG).

Exclusion criteria

Exclusion criteria: Patient who is not willing to give voluntary informed consent. Women of age less than 18 years and more than 40 years. Patient with chronic systemic illness (cardiac failure, hypertension, diabetes mellitus, tuberculosis, chronic renal disease). Patient with carcinoma of reproductive organs.

Design outcomes

Primary

Measure	Time frame
To explore the effectiveness of Shatapushpa churna along with Shatpushpa taila nasya in the management of Artava Dushti w.s.r to Polycystic ovarian syndrome (PCOS) and compare with modern medicine.Timepoint: 90 days	—

Secondary

Measure	Time frame
1. To determine the efficacy of the interventions on LH, FSH levels in the management of polycystic ovarian syndrome (PCOS). 2. To determine the efficacy of interventions on changes in size & volume of ovary in Polycystic ovarian syndrome (PCOS)Timepoint: 90 days	—

Countries

India

Contacts

Public ContactProf Rajesh Kumar Gupta

Post Graduate Institute of Ayurveda PGIA Jodhpur Rajathan India 342037

guptadrrajeshkumargupta@gmail.com9636520573

Outcome results