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

Phase 1/2

Not yet recruiting

• Conditions: Follicular cyst of ovary. Ayurveda Condition: ARTAVAKSHAYAH, (2) ICD-10 Condition: E888||Other specified metabolic disorders. Ayurveda Condition: ARTAVAKSHAYAH,

• Registration Number: CTRI/2023/02/050057
• Lead Sponsor: Dr Sonu Mariam Rajan

Brief Summary

The study is 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 ARTAVAKSHAYA in 30 patients, will be held in SRI SRI COLLEGE OF AYURVEDIC SCIENCE AND RESEARCH HOSPITAL BENGALURU, KARNATAKA IN PRASUTI TANTRA AND STREE ROGA DEPARTMENT. The primary outcome measures will be reduction of number of follicular cyst and regularise menstrual cycle, secondary outcome measures will be normalise the LH and FSH ratio.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-02-23
• Study Start: 2023-02-25

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in no of ovarian cysts and regularize the menstrual cycles.	12 weeks

Secondary Outcome Measures

Name	Time	Method
normalize the LH:FSH ratio	12 weeks

Trial Locations

Locations (1)

PTSR department. Room no -10. Sri sri college of ayurvedic science and research hospital, Bangalore.; 🇮🇳 Bangalore, KARNATAKA, India

PTSR department. Room no -10. Sri sri college of ayurvedic science and research hospital, Bangalore.

🇮🇳Bangalore, KARNATAKA, India

Dr Sonu Mariam Rajan

Principal investigator

9986783079

sonumariamrajan@gmail.com