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A Clinical Study on Vandhyakarkotaki Gel for Breast Engorgement After Delivery

Evaluation of the Effect of Vandhyakarkotaki Gel in Breast Engorgement (Stanashotha) in Postnatal Women: A Single-Arm Clinical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108445
Enrollment
46
Registered
2026-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O922- Other and unspecified disorders ofbreast associated with pregnancy and the puerperium

Interventions

None listed

Sponsors

Dr Mahima Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Lactating Mother From 1-45 Days 2.Full Term Normal Vaginal Delivery and Lower Segment C-section 3.Lactating mothers who Are Suffering from Symptoms Such as Heaviness (Guruta), Swelling (Shotha), Tenderness (Sparshasahatva) In Breast.

Exclusion criteria

Exclusion criteria: 1. Antenatal Patients 2. Patients With Past or Present Malignancy. 3. Fibrocystic Changes 4. Breast Lumps 5. Breast Abscess

Design outcomes

Primary

MeasureTime frame
Reduction in symptoms Swelling (shoth) Pain (Shoola) tenderness (Sparshasahatva) Redness(Aaraktvarnata) in breast engorgement ( Stanyashotha)Timepoint: baseline day 0, 3rd day, 6th day—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Mahima Sharma

Dr. D. Y. Patil College Of Ayurved, Hospital And Research Centre, Pimpri, Pune-411018

bhonsalesmritika@gmail.com9850967067

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026