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Clinical Trials/CTRI/2024/06/069634
CTRI/2024/06/069634
Not yet recruiting
Phase 1

A Clinical Study To Evaluate The Combined Efficacy Of Sahacharadi Taila Matra Basti with Oral Administration OF Shatpushpa Churna In The Management Of Artavkshaya Due To Polycystic Ovarian Syndrome

Dr Ashvini Zore1 site in 1 country30 target enrollmentStarted: July 20, 2024Last updated:

Overview

Phase
Phase 1
Status
Not yet recruiting
Sponsor
Dr Ashvini Zore
Enrollment
30
Locations
1
Primary Endpoint
To see the efficacy of Sahacharadi Taila Matrabasti with oral administration of Shatapushpa Churna in the management of Artavkshaya due to PCOS

Overview

Brief Summary

Article not yet published

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 35.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • Subject of age group 18 to 35 years irrespective of marital status Subject fulfilling diagnosis criteria Amenorrhoea for more than 35 days to 60 days.

Exclusion Criteria

  • Subject with primary Amenorrhoea Subject having any acute infection or any systemic major disease Pregnancy Subject who are Basti Anarha according to Ayurveda.

Outcomes

Primary Outcomes

To see the efficacy of Sahacharadi Taila Matrabasti with oral administration of Shatapushpa Churna in the management of Artavkshaya due to PCOS

Time Frame: 4 weeks

Secondary Outcomes

  • To determine the change in ovarian volume.

Investigators

Sponsor
Dr Ashvini Zore
Sponsor Class
Other [Other ( Gov Grant In Aid Ayurveda College]
Responsible Party
Principal Investigator
Principal Investigator

Ashvini Diliprao Zore

Seth Govindji Raoji Ayurved Mahavidyalaya

Study Sites (1)

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