Effectiveness of Soothagathadaiudaippu kudineer chooranam for irregular periods

Clinical Evaluation of Soothagathadai udaippu Kudineer Chooranam in the management of Soothagavayu(Polycystic Ovarian Syndrome)-A Pilot Study

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/02/049690

Enrollment

Registered

2023-02-14

Start date

Unknown

Completion date

Unknown

Last updated

2023-03-06

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: Soothagathadaiudaippu kudineer chooranam: Dosage:5gram of powder into 60ml decoction twice a day Duration:90 days Control Intervention1: nil: nil

Eligibility

Inclusion criteria

Inclusion criteria: Married / unmarried women aged between 15-35 years Amenorrhoea / oligomenorrhoea Irregular menstruation Hirsutism Polycystic ovary in ultrasound (Unilateral / Bilateral). Patients who are willing to co-operate for specific and routine blood investigations. Patients who are willing to sign informed consent.

Exclusion criteria

Exclusion criteria: Hyperthyroidism /Hypothyroidism Congenital uterine defects Pituitary /adrenal disorders Haemorrhagic / chocolate cyst Breast feeding mothers Tuberculosis of ovary or uterus Any other systemic illness

Design outcomes

Primary

Measure	Time frame
The outcome is to find the effectiveness of Soothagathadaiudaippu kudineer chooranam for Soothagavayu(Polycystic overian syndrome) which will be assessed by rotterdam criteria after 12 weeksTimepoint: 12 weeks	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactDr D Manikandan

National Institute of Siddha

mmssiddha@rediffmail.com09444214582

Outcome results

None listed

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