To study effect of jyotishmatyadi vati in delayed menses

An open labelled single arm clinical study of jyotishmatyadi vati in nashtartava with special reference to delayed menses

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/10/021824

Enrollment

Registered

2019-10-30

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: N912- Amenorrhea, unspecified

Interventions

Intervention1: Jyotishmatyadi vati: DOSE 1 gm BD DOSAGE FORM TABLET ROUTE ORAL TIME TWICE A DAY ANUPANA DUGDHA DURATION 3 DAYS FOLLOW UP 8 AND 15 the day Control Intervention1: Not applicable: Not app

Eligibility

Inclusion criteria

Inclusion criteria: Married and unmarried females with missed period and negative upt

Exclusion criteria

Exclusion criteria: Patient having H/o injectable contraceptive s in recent time Patient having major illness causing weight loss Patient having uterine anamolies Patient having pregnancy Patient having primary amenorrhea Patient with surgical amenorrhea Patient with severe anaemia

Design outcomes

Primary

Measure	Time frame
effect of jyotishmatyadi vati in nashtartavaTimepoint: 2 months	—

Secondary

Measure	Time frame
Observation of adverse effects of jyotishmatyadi vatiTimepoint: 18 months	—

Countries

India

Contacts

Public ContactDr Deepali Suresh Rajput

Saneguruji aarogya Kendra

drdeepalirajput@yahoo.com9423978584

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026