To study the effect of Tila decoction in Artavkshay with special reference to oligomenorrhea and hypomenorrhea

A Clinical Study to assess the effect of TilaKashay in the management of Artavkshay with special reference to Oligomenorrhoea and Hypomenorrhoea. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/066565

Enrollment

Registered

2024-04-30

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: 1.Patients fulfilling cardinal symptoms of Artavkshay, i.e. a) Interval between 2 menses more than 35 days b) Duration of menstrual bleeding less than 2 days c) Menstrual Pain 2. Both married and unmarried women.

Exclusion criteria

Exclusion criteria: 1.Patient with Menorrhagia. 2.Pregnant and Lactating Amenorrhoea. 3. Hb Count less than 8gm/dl 4.Congenital Anomalies of uterus or ovaries. 5.Women with any malignancy, uterine fibroid, uterine polyp, endometriosis.

Design outcomes

Secondary

Measure	Time frame
1. To study the effect of Tilakashay on Endomentrial thicknessTimepoint: 3 months I.e 12 weeks	—

Primary

Measure	Time frame
To assess the effect of Tilakashay in the management of Artavkshay with special to Oligomenorrhoea and Hypomenorrhoea 1)To evaluate the duration of intermenstrual phase. 2) To evaluate the duration of menstrual phase. 3) To evaluate the amount of menstrual bleeding.Timepoint: Treatment will be given for 3 months I.e for 12 weeks	—

Countries

India

Contacts

Public ContactDr Mangesh Laxman Patil

Ymt ayurvedic medical college and hospital kharghar navi mumbai

chitrangiwagh@yahoo.com8976244248

Outcome results