| CTRI Number |
CTRI/2026/01/101084 [Registered on: 14/01/2026] Trial Registered Prospectively |
| Last Modified On: |
14/01/2026 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Biological Diagnostic Preventive |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
Effect of applying mother’s breast milk into the nose on infection-related germs in premature babies receiving breathing support |
|
Scientific Title of Study
|
Effect of intranasal breast milk instillation on nasal bacterial colonization in preterm neonates on non-invasive ventilation: a randomized controlled trial |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr SHIVI SAXENA |
| Designation |
DM senior resident |
| Affiliation |
Government medical college and hospital, sector 32, Chandigarh |
| Address |
D block, 4th floor, Department of Neonatology, government medical college and hospital, sector 32, chandigarh.
Pincode: 160030
Chandigarh CHANDIGARH 160030 India |
| Phone |
9023665316 |
| Fax |
|
| Email |
peds.shivisaxena.2020@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr SUKSHAM JAIN |
| Designation |
Professor |
| Affiliation |
Government medical college and hospital, sector 32, Chandigarh |
| Address |
D block, 4th floor, Department of Neonatology, government medical college and hospital, sector 32, Chandigarh
Pincode: 160030
Chandigarh CHANDIGARH 160030 India |
| Phone |
9988901596 |
| Fax |
|
| Email |
dr.sukshamj@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr SHIVI SAXENA |
| Designation |
DM senior resident |
| Affiliation |
Government medical college and hospital, Chandigarh |
| Address |
D block, 4th floor, Department of Neonatology, government medical college and hospital, sector 32, Chandigarh
Chandigarh CHANDIGARH 160030 India |
| Phone |
9023665316 |
| Fax |
|
| Email |
peds.shivisaxena.2020@gmail.com |
|
|
Source of Monetary or Material Support
|
| Government medical college and hospital
Sector 32 Chandigarh |
|
|
Primary Sponsor
|
| Name |
Government medical college and hospital Chandigarh |
| Address |
Government medical college and hospital
Sector 32 Chandigarh |
| Type of Sponsor |
Government medical college |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr SHIVI SAXENA |
Government medical college and hospital, Chandigarh |
Neonatal intensive care unit and intermediate care nursery, Government medical college and hospital, sector 32, Chandigarh. Chandigarh CHANDIGARH |
9023665316
peds.shivisaxena.2020@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| INSTITUTIONAL ETHICS COMMITTEE (GMCH, Chandigarh) |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: P220||Respiratory distress syndrome of newborn, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
Human breast milk |
Intranasal breastmilk instillation for those neonates requiring non invasive ventilation. Breast milk to be taken from neonate’s own mother and intervention will be started from 6 hours of life till the neonate is on non invasive ventilation |
| Comparator Agent |
No agent |
The second arm will be those neonates who are on non invasive ventilation but no intervention (intranasal breast milk instillation) will be done. They will receive standard care. |
|
|
Inclusion Criteria
|
| Age From |
1.00 Day(s) |
| Age To |
2.00 Month(s) |
| Gender |
Both |
| Details |
All babies born with gestation age 27+0 to 32+6 weeks requiring NIV within 48 hours of life will be enrolled |
|
| ExclusionCriteria |
| Details |
1. Babies with severe congenital malformation or chromosomal anomalies
2. Structural anomalies like choanal atresia, cleft palate with nasal involvement, nasal septal deviation or facial trauma at birth
3. Infants receiving intranasal medications other than nasal saline drops
4. Refuse to give consent.
5. Neonates with confirmed or suspected congenital syphilis (especially infants presenting with nasal discharge or “snuffles”).
6. Neonates with suspected TORCH infections
7. Severe birth asphyxia ( APGAR less than or equal to 3 at 5 minutes) |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Sequentially numbered, sealed, opaque envelopes |
|
Blinding/Masking
|
Investigator Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
| Effect of intranasal breast milk application on bacterial colonization patterns in nasal cavity of preterm neonates with gestation age 27 +0 to 32 +6 weeks on non-invasive ventilation |
Before starting non invasive ventilation till the neonate is on non invasive ventilation |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| failure of non-invasive ventilation and it’s overall duration |
From start of non invasive ventilation till its failure or weaning |
| rate of infections, including ventilator-associated pneumonia (VAP) and sepsis |
From the start till weaning of non invasive ventilation |
| neurological outcomes, including MRI brain and neurodevelopmental assessment age using the HINE or ASQ-3 (in case of loss to follow-up). |
MRI At 40 weeks corrected gestation age and neurodevelopment assessment at 3 -5months corrected gestation age |
| incidence of other major neonatal morbidities |
During hospital stay |
|
|
Target Sample Size
|
Total Sample Size="110" Sample Size from India="110"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
31/01/2026 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="1" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - YES
- What data in particular will be shared?
Response (Others) -
- What additional supporting information will be shared?
Response - Study Protocol Response - Informed Consent Form
- Who will be able to view these files?
Response - Researchers who provide a methodologically sound proposal.
- For what types of analyses will this data be available?
Response (Others) -
- By what mechanism will data be made available?
Response (Others) - On demand by email
- For how long will this data be available start date provided 30-12-2028 and end date provided 31-12-2029?
Response (Others) - One year after publication
- Any URL or additional information regarding plan/policy for sharing IPD?
Additional Information - NIL
|
|
Brief Summary
|
This study is a parallel group randomized controlled trial conducted in the Neonatal Intensive Care Unit of Government Medical College and Hospital Chandigarh. The study aims to evaluate the effect of intranasal instillation of mothers own breast milk on nasal bacterial colonization patterns in preterm neonates receiving non invasive ventilation. Preterm infants with gestational age between 27 plus 0 and 32 plus 6 weeks who require non invasive ventilation within the first 48 hours of life will be enrolled after obtaining written informed consent from parents. Eligible neonates will be randomized into two groups. The intervention group will receive intranasal instillation of mothers own breast milk at a dose of 0.1 ml in each nostril three times daily until discontinuation of non invasive ventilation. The control group will receive standard nasal care as per unit protocol. Both groups will otherwise receive identical standard neonatal care. Nasal swabs will be collected at baseline within two hours of starting non invasive ventilation before the first intervention then at 24 to 48 hours and again on day seven or at discontinuation of non invasive ventilation whichever occurs later. The primary outcome is the pattern of nasal bacterial colonization including commensal and pathogenic organisms assessed by culture and sensitivity testing. Secondary outcomes include duration and failure of non invasive ventilation incidence of ventilator associated pneumonia clinical and culture proven sepsis and other major neonatal outcomes such as necrotizing enterocolitis bronchopulmonary dysplasia retinopathy of prematurity intraventricular hemorrhage feeding intolerance and mortality before discharge. Neurodevelopmental outcomes will be assessed at three to five months corrected age using standardized tools and brain volume assessment on MRI at term equivalent age will be performed in a subset of infants. The study hypothesizes that intranasal application of breast milk will favorably modify nasal microbial colonization by increasing commensal flora and reducing pathogenic organisms through local mucosal immunomodulatory effects. The findings of this study may provide evidence for a simple low cost intervention to reduce respiratory infections and improve outcomes in preterm neonates on non invasive ventilation.
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