To study the efficacy of ushir churna with godugdha in decreased milk secretion .

An open randomized controlled clinical study to evaluate the efficacy of ushir churna with godugdha in stanyakshaya. - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/082285

Enrollment

100

Registered

2025-03-13

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Health Condition 1: O924- Hypogalactia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: IN MOTHER 1)Patients willingly participating in the trial and giving informed written consent form. 2)Age group of patients between 21 to 35 years 3)Patients having sign and symptoms of stanyakshaya . 4)Patients from third day of Post partum (both LSCS and FTND) 5) Patients irrespective of primigravida or multigravida were selected. IN BABY 1) Full term normal weight (2.5 to 3.5kg) mother side baby.

Exclusion criteria

Exclusion criteria: IN MOTHER 1)Cracked or flat nipples. 2)Mastitis 3) History of breast trauma and surgery. 4) Patient under epileptic and Psychotic drugs. IN BABY 1)Low birth weight baby(not allowing breast milk).

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Ushir Churna with Godugdha in StanyakshayTimepoint: On 7th day, 15th day , 30th day	—

Secondary

Measure	Time frame
1)To increase Breastmilk secretion. 2)To assess stanza vruddhi by subjective parameter. 3)To study stanyakshaya in detail as per Ayurveda 4)To achieve the outcome of study in 7 days.Timepoint: On 7th day , 15th day, 30th day	—

Countries

India

Contacts

Public ContactKalyani Harishchandra Sapkal

Yashwant Ayurvedic College Postgraduate training and Research centre Kodoli, District Kolhapur

dr.chodankarsmita@gmail.com8888721639

Outcome results