Efficacy of Vayasthapana Gana and Rasayanakalpa Vati on Menopausal syndrome

Phase 2

Completed

• Conditions: Patients who suffering from Menopausal syndrome

• Registration Number: CTRI/2015/07/006044
• Lead Sponsor: INSTITUTE FOR POST GRADUATE TRAINING AND RESEARCH IN AYURVEDA

Brief Summary

My study is on Menopausal syndrome.Drugs used for study are Vayasthapangana Ghanvati and RasayankalpaVati.vayasthapanagana Ghanavati is trial drug and rasayankalpaVati is proved drug for Menopausal syndrome.Both drugs given to the  female patients age group between 40 to 50 years for 2 month by random sampaling method by toss and coin is done..Before study started each patient is gone for investigation process.Ultrasound done for endometrium thickness.routine heamatological and urine  routine and microscopic examination done.Hormonal essay is also done.serum follical stimulating hormone and serum oestradiol are done.if patient fulfill all the above criteria then medicine is given for two month.Vayasthapanaganaghanavti 2 tablets(500mg) bd are given with milk before empty stomach.Rasayankalpavati 5 tablets(500mg) bd are given with milk before empty stomach.follow up is taken for one month of each patient.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-03-13
• Study Completion: 2015-02-27
• Last Update Posted: 2019-09-22

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 34

Inclusion Criteria

• Amenorrhoea at least for 12 months or more.
• Kupperman Menopausal Index Score ≥ 15 FSH ≥ 20 IU/L Thickness of endometrium ≤ 5 mm by USG finding.

Exclusion Criteria

• Age below 40 years and age more than 55 years.
• Women with uncontrolled medical conditions e.g. Hypertension, Heart disease, Diabetes mellitus, Cancer.
• Who had the H/O Hormone replacement therapy (HRT).
• Women having H/O excessive and/or irregular bleeding per vaginally.Established case of mental illness.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
TO EVALUATE AND COMPARE THE EFFICACY OF BOTH TRIAL DRUGS IN MENOPAUSAL SYNDROME	2 months in both groups

Secondary Outcome Measures

Name	Time	Method
To improve the quality of life of menopausal women	2 months in both groups

Trial Locations

Locations (1)

Institute of postgraduate teaching and research in ayurveda; 🇮🇳 Jamnagar, GUJARAT, India

Institute of postgraduate teaching and research in ayurveda

🇮🇳Jamnagar, GUJARAT, India

Dr Krutika Chaudhari

Principal investigator

9429012309

chaudhari_krutika88@yahoo.com