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To study the efficacy of Yashtimadhu Siddha Taila Anuvasana Basti with Yonipichu in 9th month of pregnancy for Sukhprasav (Normal Labour)

Randomized Controlled Trial to study the efficacy of Yashtimadhu Siddha Taila Anuvasana Basti with Yonipichu in 9th month of pregnancy for Sukhprasav (Normal Labour) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078174
Enrollment
100
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

None listed

Sponsors

Sane Guruji Arogya Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Primipara women with SLIUF (Single Live Intra Uterine Foetus) with 36 weeks of gestation. 2. Normal foetal position at term.

Exclusion criteria

Exclusion criteria: 1. Pregnancy associated with any pre-existing or pregnancy induced systemic diseases like Essential Hypertension, Diabetes Mellitus, Liver related disorders, Kidney related disorders, Heart related disorders, Asthma, Blood related disorders like Thalassemia, Sickle cell anaemia, GDM (Gestational Diabetes Mellitus), Pre-eclampsia or Eclampsia or associated with any immunocompromised illness. 2. Pregnancy associated with placental abnormalities like Placenta previa, Circumvallate placenta, etc. and foetal anomalies like Hydrocephalus, Polyhydramnios, Oligohydramnios, Mal-presentation of foetus. 3. Pregnancy associated with Reproductive tract abnormalities and pelvic abnormalities.

Design outcomes

Primary

MeasureTime frame
To evaluate the combined effect of Yashtimadhu Siddha Taila Anuvasana basti with Yonipichu in Primipara women from 36 weeks of pregnancy till delivery for Sukhprasav (Normal Labour)Timepoint: Administration of Yashtimadhu Siddha Taila Anuvasana Basti with Yonipichu on each visit and on every 4th day till delivery Administration will be done in Primipara women from 36th week or on completion of 35th week of pregnancy till delivery Follow up and assessment will be done—

Secondary

MeasureTime frame
Literature study of Garbhini Paricharya To look for Adverse effects if anyTimepoint: Study will be done using Ayurvedic Granthas & modern texts Preparation of drugs will be done according to the standard procedure During the regimen observation will be done for any adverse effects if any—

Countries

India

Contacts

Public ContactDr Jigisha Hitesh Tanna

MAM S Sumatibhai Shah Ayurved Mahavidyalaya

mandaghorpade@yahoo.com9822007570

Outcome results

None listed

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