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To study effect of lakshadi tail abhyanga in preterm babies for normal growth

Randomized controlled trial to study effect of lakshadi tail abhyanga in late preterm babies for normal growth - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078450
Enrollment
90
Registered
2024-12-23
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

None listed

Interventions

None listed

Sponsors

Sane Guruji Arogya Kendra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Neonates with gestational age equal to 34.1 weeks to 36.6 weeks.3 Neonates with birth weight in between 1800gm to 2400gm. Babies who are haemodynamically stable. Neonates who are on full feed. Those who are passing patch test will be included Both male and female child will include in this study Parents who will give informed written consent those baby will be included in the study

Exclusion criteria

Exclusion criteria: Neonates having respiratory distress Hypoglycemia those who are receiving supplementary oxygen ventilatory support and having neurological problems Neonates with major congenital anomalies at birth like cleft palate cleft lip imperforated anus diaphragmatic hernia cyanotic heart disease Tracheo oesophageal fistula Those who are having neonatal sepsis Jaundice fever will be excluded Those are having skin disorders will be excluded

Design outcomes

Primary

MeasureTime frame
To study effect of lakshadi tail abhyanga in late preterm babies for normal growthTimepoint: Treatment will be given for 1 month Abhyanga will be done for once in a day for 1 month Follow up and assessment will be done pre treatment and 5th 15th 30th 45th days

Secondary

MeasureTime frame
Literature study of akala prasut balak in both modern & ayurvedic textbookTimepoint: Study will be done using Ayurvedic Granthas & modern text preparation of drugs will be done according to standard procedure During treatment observation will be done on day 5th 15th 30th 45th day for any adverse effect on patient

Countries

India

Contacts

Public ContactDr Manisha Jagtap

MAM S Sumatibhai Shah Ayurved Mahavidyalaya Malwadi Hadapsar Pune

Manisha.shinde18@gmail.com8412022555

Outcome results

None listed

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