A clinical study on effect of basti yonipurana and nasya in the management of prasava

A clinical study on effect of basti yonipurana and nasya in the management of prasava - Labour

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2016/06/007057

Enrollment

Registered

2016-06-29

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- vertex presentation, age between 18 to 35 years, after completed 8th months of pregnancy

Interventions

Intervention1: Shodhan Basti,Yonipurana,Nasya: Basti with dashmoola taila 60ml + 200ml of panchakola, vasa,haritaki kwatha given 3 days alternatively through anal route in the morning empty stomach y

Eligibility

Inclusion criteria

Inclusion criteria: • All primi and multi pregnant women with vertex presentation, age group 18-35 year and complete 8th month of pregnancy. • Patients with clinically absent of CPD (Cephalo pelvic disproportion).

Exclusion criteria

Exclusion criteria: • Patients age group between 35 year • Known case of C.P.D • Mal-presentation. • Oligohydramnios. • APH ( Anti partum haemorrahge) • Pregnancies complicated by jaundice, eclampsia, pre-eclampsia, twins

Design outcomes

Primary

Measure	Time frame
normal deliveryTimepoint: normal delivery	—

Secondary

Measure	Time frame
normal deliveryTimepoint: 3 days	—

Countries

India

Contacts

Public Contactdr shilpa donga

ipgt and ra jamnagat

deilaxmipriya@yahoo.com9228198366

Outcome results

None listed

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