A clinical study to asses the effect of shunti in case of disease primary Dysmenorrhoea

A conceptual study on shoolaprashamana gana and clinical Evaluation of Shunti in Kashtartava with special reference to primary Dysmenorrhoea - nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/04/051380

Enrollment

Registered

2023-04-06

Start date

Unknown

Completion date

Unknown

Last updated

2023-05-01

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

Conditions

Health Condition 1: N944- Primary dysmenorrhea

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Subjects suffering form kashtaartava having classical signs and symptoms. subjects willing and able to participate in the study

Exclusion criteria

Exclusion criteria: Subjects who are not willing for the clinical study. Subjects suffering from acute systemic disorders. subjects who belong to pitta prakriti will be excluded.

Design outcomes

Primary

Measure	Time frame
pain reduction Timepoint: 20days	—

Secondary

Measure	Time frame
Reduction of pain during mensesTimepoint: 3 months	—

Countries

India

Contacts

Public ContactDr Renuka M Tenahalli

BLDEAS AVS AYURVEDA MAHAVIDYALAYA VIJAYPURA

rbjumanal@gmail.com9535268559

Outcome results