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To know the efficacy of patoladi kwatha along with navaka guggulu in polycystic ovarian syndrome

A randomized open labelled controlled clinical study to evaluate the efficacy of patoladi kwatha along with navaka guggulu in polycystic ovarian syndrome with special reference to â??artavakshayaâ??

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/050057
Enrollment
30
Registered
2023-02-24
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: N830- Follicular cyst of ovary Health Condition 2: E888- Other specified metabolic disorders

Interventions

None listed

Sponsors

Dr Sonu Mariam Rajan
Lead Sponsor
Dr Rachana H V
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects between the age group of 18 years to 40 years, irrespective of marital status. 2. Subjects with Rotterdam criteria. 3. Subjects presenting with the classical symptoms of Artavakshaya. 4. Subjects presenting with the symptoms of oligomenorrhea, secondary amenorrhea or hypomenorrhea. 5. Polycystic ovary (5 or more follicles in at least one ovary measuring 2-9mm) confirmed with USG

Exclusion criteria

Exclusion criteria: 1. Subjects with primary amenorrhea. 2. Subjects using of oral contraceptives (current or within the last 3 months). 3. Subjects with menorrhagia, metrorrhagia, menometrorrhagia will be excluded. 4. Subjects suffering from malignancies and chronic systemic diseases.

Design outcomes

Primary

MeasureTime frame
Reduction in no of ovarian cysts and regularize the menstrual cycles.Timepoint: 12 weeks

Secondary

MeasureTime frame
normalize the LH:FSH ratioTimepoint: 12 weeks

Countries

India

Contacts

Public ContactDr Sonu Mariam Rajan

Sri sri college of ayurvedic science and research hospital, kanakapura road, udayapura, bengaluru

dr.rachanabhat@gmail.com9535744077

Outcome results

None listed

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