Management in Nonobese PCOS through Ayurveda

Efficacy of Nitya Virechana with Naracha Choorna,Shatapushpa Taila Matrabasti and Shatavari-Yashtimadhu Choorna orally in the management of Artavadushti w.s.r to Non-obese Polycystic Ovarian Syndrome:A Single Arm Open Labelled Clinical Trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/04/051682

Enrollment

Registered

2023-04-17

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-01

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

Conditions

Health Condition 1: N915- Oligomenorrhea, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Both married /unmarried patients in the age group of 18-40 yrs. 2. Patients with any 3 or more clinical features of PCOS like- • Amenorrhea or Oligomenorrhoea • Anovulation • Acne • Hirsutism 3. Along with confirmation of polycystic ovary in USG finding. 4. BMI <=25 kg/m2

Exclusion criteria

Exclusion criteria: 1. Age group 40yrs 2. BMI >25 Kg/m2 3. Patients suffering from chronic Pelvic diseases like (Endometriosis, PID, Uterine Fibroid, Menorrhagia, etc.) 4. Organic lesions of reproductive tract like Tuberculosis, Carcinoma and congenital deformities.

Design outcomes

Primary

Measure	Time frame
It is Expected that trial drugs will help in the reduction of ovarian volume. Timepoint: 60 days	—

Secondary

Measure	Time frame
Secondary outcome: It is expected that trial drugs will help in the regulation of menstrual pattern and ovulation.Timepoint: 2 months	—

Countries

India

Contacts

Public ContactProf Neha Pandya

Institute of Teaching and Research in Ayurveda

drshilpadonga@yahoo.com9825646796

Outcome results