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Anuvasan Vati and Yoni Picchu in Sukha Prasava

A clinical study of Anuvasan Vati and Yoni Picchu in Sukha Prasava - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087488
Enrollment
30
Registered
2025-05-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: Anuvasana Vasti and Yoni Picchu: Anuvasana Vasti Dose- 50 ml twice in a week Duration - one month Yoni Picchu Dose - 10 ml daily Duration - one month Control Intervention1: Anuvasana

Sponsors

Government Ayurvedic College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient willing for trail 2 The Subject willing to cooperate in the study 3 Subject having age between 18 to 35 years both age included 4 Gestational age lies between 32-37 week preferences to primigravida 5 The subject free from chronic psychosomatic illness and its secondary complication

Exclusion criteria

Exclusion criteria: 1 Patients with age group less than 18 years and greater than 37 years 2 Patients having contracted pelvis, malpresentation 3 Systemic Chronic illness like diabetes mellitus, tuberculosis, jaundice etc 4 Any sort of Eclampsia, Preeclampsia. 5 Any sort of Tachycardia, Bradycardia, Hypertension etc 6 Any type of mental disorder like epilepsy might be excluded from the study

Design outcomes

Primary

MeasureTime frame
Relief from sign and symptomsTimepoint: 30 days

Secondary

MeasureTime frame
Determination of effects of intervention w.r.t othersTimepoint: 30 days

Countries

India

Contacts

Public ContactDr Rinki Kumari

Government Ayurvedic College and Hospital

dr.prabhapandey@yahoo.in7004860634

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026