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A Randomized Controlled Trial Comparing Continuous, Standard Bolus, and Accelerated Continuous Enteral Feeding in Neonates Weighing Less Than 1.8 kg

A Three-Arm, Parallel-Group Randomized Controlled Trial Comparing Continuous, Standard Bolus, and Accelerated Continuous Enteral Feeding in Neonates with Birth Weight less than 1.8 kg - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/102715
Enrollment
180
Registered
2026-02-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: P84- Other problems with newborn

Interventions

Intervention1: Arm 1 Continuous Enteral Feeding Arm: Arm 1: Continuous Enteral Feeding Neonates weighing less than 1.8 kg will receive continuous enteral feeding via nasogastric tube using a feeding p

Sponsors

KRITI SHOKEEN
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Neonates with a birth weight less than 1.8kg eligible for nasogastric (NG)feeding admitted in NICU hemodynamically stable and eligible to start enteral feeding as per unit protocol

Exclusion criteria

Exclusion criteria: Major congenital anomalies, particularly gastrointestinal anomalies Severe perinatal asphyxia Conditions contraindicating enteral feeding (e.g., necrotizing enterocolitis at baseline)

Design outcomes

Primary

MeasureTime frame
To compare the time (in days) to achieve full enteral feeds (150 ml/kg/day) across the three feeding regimensTimepoint: Assessed daily from initiation of enteral feeding until achievement of full enteral feeds (150 ml/kg/day) or till discharge, whichever is earlier

Secondary

MeasureTime frame
Secondary: 1. To compare the rate of weight gain (g/kg/day) among neonates receiving the three feeding regimens. 2. To look for development of complications Necrotizing enterocolitis, incidence of apnoea, any incidence of Sepsis) 3. To assess the length of hospital stay among the groupsTimepoint: 1- Assessed daily during hospital stay until discharge or attainment of full enteral feeds. 2-Assessed throughout the hospital stay until discharge. 3-Recorded at the time of Discharge

Countries

India

Contacts

Public ContactKRITI SHOKEEN

MGM MEDICAL COLLEGE, AURANGABAD, MAHARASHTRA

SHOKEENKRITI2698@GMAIL.COM7768907662

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026