A Clinical study for the effectiveness of Vidarikanda Churna with Godugdha in Stanyakshay

A Clinical trial to evaluate the effectiveness of Vidarikanda Churna with Godugdha in the Management of Stanyakshay - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/06/088534

Enrollment

Registered

2025-06-10

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: E898- Other postprocedural endocrine andmetabolic complications and disorders

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Mothers suffering from Stanyakshya symptoms like Stanyamlanata and Stanyasambhavalpata having age group between 18 - 40 years. 2. Mother having baby up to 12 months will be selected for study. 3. Patients who are willing to give consent for this study.

Exclusion criteria

Exclusion criteria: 1. Known case of breast abscess, Mastitis, cysts and tumours of breast, cracked nipples and breast cancer. 2. Patients suffering from Stanyakshaya due to any secondary cause like HIV, TB.

Design outcomes

Primary

Measure	Time frame
Mothers suffering from Stanyakshya will get relief from symptoms like Stanyamlanata after 4 wekksTimepoint: Mothers suffering from Stanyakshya will get relief from symptoms like Stanyamlanata after 4 weeks	—

Secondary

Measure	Time frame
relief from symptomsTimepoint: 2 weeks	—

Countries

India

Contacts

Public ContactDR SNEHAL RATHOD

GOVT AYURVED COLLEGE, SAKKARDARA, NAGPUR

dr.adbombarde67@gmail.com9970115160

Outcome results