Study The Effect Of Ayurvedic Formulation In Artavkshaya (scanty menses)

A Single Arm Clinical Study To Evaluate The Efficacy Of Ayurvedic Formulation In Artavkshaya - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067477

Enrollment

Registered

2024-05-16

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N915- Oligomenorrhea, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Duration of Menstrual bleeding flow of 2 days or less Patient with reduced quantity of menstrual flow Patient with increased intermenstrual period more than 35 days Age group of female between 20 to 40 years will be selected (Inclusive both years)

Exclusion criteria

Exclusion criteria: Women Suffering with gross structural abnormalities of uterus and overy. Systemic illness like Diabetes Mellitus, Thyroid function, Hypertension, any type of malignancy.

Design outcomes

Primary

Measure	Time frame
To assess the efficacy of Ayurvedic Formulation in management of ArtavkshayaTimepoint: 60 days before menstrual cycle upto 1st day of during menstrual cycle for 2 consecutive menstrual cycles (Follow up for 2 consecutive menstrual cycles)	—

Secondary

Measure	Time frame
To Observe The Adverse Effect of Ayurvedic Formulation in Artavkshaya If AnyTimepoint: 60 days before menstrual cycle upto 1st day during menstrual cycle for 2 consecutive menstrual cycles (Follow up for 2 consecutive menstrual cycles)	—

Countries

India

Contacts

Public ContactDr Jayashree Patil

Dr D Y Patil college of Ayurveda and Research Centre

jayupa.patil6@gmail.com9921244690

Outcome results