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MANAGEMENT OF ARTAVA DUSHTI W.S.R TO POLYCYSTIC OVARIAN SYNDROME WITH AROGYAVARDHINI RASA AND PATHADI CHOORNA.

Management of Artava dushti w.s.r to Polycystic ovarian syndrome with Arogyavardhini rasa and Pathadi choorna: A single arm open labelled clinical trial.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/030954
Enrollment
60
Registered
2021-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: Arogyavardhini rasa and pathadi choorna: Arogyavardhini rasa 250 mg along with Pathadi choorna 5gm given orally on empty stomach both morning and evening with lukewarm water for a peri

Sponsors

IPGT AND RA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Both married /unmarried patients in the age group of 18-40yrs. Patients with any 3 or more clinical features of PCOS like- Amenorrhea or Oligomenorrhoea Anovulation Infertility (Due to anovulation) Acne Hirsutism (Ferriman-Gallwey scale) Obesity (BMI above 25) Acanthosis nigricans Along with confirmation of any one Polycystic Ovary in USG finding.

Exclusion criteria

Exclusion criteria: 1. Patients suffering from Pelvic/Systemic diseases like (Endometriosis, Hydrosalpinx, Fibroid uterus,). 2. Organic lesions of reproductive tract like T.B, Carcinoma and Congenital deformities. 3. Patients with history of Cardiac diseases, Chronic liver disease. 4. Age group 40yrs will be excluded. 5. Uncontrolled Hypertension (Systolic BP above 150 & Diastolic above100mmhg), Uncontrol led Diabetes mellitus (above the range of 160-200 mg/dl, FBS)

Design outcomes

Primary

MeasureTime frame
It is expected that trial drug help to improve anovulation ,oligoovulation ,hirsutism ,amenorrhea ,acne ,infertility, obesityTimepoint: 4 weeks after completion of clinical trial.

Secondary

MeasureTime frame
Drug may have effect on ovulation induction and conception.Timepoint: After the followup period.

Countries

India

Contacts

Public ContactProf Laxmipriya dei

IPGT AND RA

deilaxmipriya@yahoo.com9228198366

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026