WHO ICTRP trial

Effectiveness of oral intake of Kalyanaka Ghritha in reducing mild to moderate…

CTRI/2025/04/084797 · Clinical Trials Registry India (CTRI) · Not Recruiting

Key facts

Trial ID CTRI/2025/04/084797
Public title Effectiveness of oral intake of Kalyanaka Ghritha in reducing mild to moderate Post Partum Depression
Scientific title Effectiveness Of Kalyanaka Ghritha In Mild To Moderate Postpartum Depression - NIL
Primary sponsor Nanda Devi L Self funded
Registry Clinical Trials Registry India (CTRI)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 4
Countries India
Conditions Health Condition 1: F53- Puerperal psychosis
Interventions Intervention1: Kalyanaka Ghrithm: 24 ml in two equally divided doses (12 ml in the morning and 12 ml in the evening) 1 hr before food with hot water as anupana for one month. Control Intervention1: Not Applicable: NIL
Registration date Apr 15, 2025
Target size 18
Secondary IDs NIL
Registry page ctri.nic.in

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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