Clinical Study To Evaluate The Efficacy Of Ksheerbala Tail Matrabasti In Artavkshya

A Single Arm Open Label Clinical Study To Evaluate The Efficacy Of Ksheerbala Tail Matrabasti In Artavkshya - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087192

Enrollment

Registered

2025-05-20

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: E889- Metabolic disorder, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Duration of menses less than 2 days Painful menses Amenorrhea Hypothyroidism with scanty menses

Exclusion criteria

Exclusion criteria: Volunteer having disease STD HIV HEP B Volunteer having anorectal disease like piles or fistula Volunteer having irregular or scanty menses due to anatomical defect of uterus

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Ksheerbala tail matrabasti in the management of artavkshyaTimepoint: To evaluate the efficacy of Ksheerbala tail matrabasti in the management of artavkshya for 7 days for 3 cycles .Within 3 month 3 assesment will be done.	—

Secondary

Measure	Time frame
To evaluate any other additional effect of Ksheerbala tail matrabasti in the scanty mensesTimepoint: To evaluate any other additional effects of Ksheerbala tail matrabasti in the scanty menses for 4 weeks	—

Countries

India

Contacts

Public ContactDrTeena Kadu

Ashtang Ayurved Mahavidyalaya

hrj9371@gmail.com919881466344

Outcome results