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CTRI Number  CTRI/2026/01/100571 [Registered on: 08/01/2026] Trial Registered Prospectively
Last Modified On: 24/12/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Preventive
Process of Care Changes 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   A randomized control trial on comparing tube feeding during Kangaroo Mother Care versus lying down in supine position to assess feed intolerance in preterm and Low Birth Weight newborns having birth weight less than 1500 g 
Scientific Title of Study   Efficacy of gavage feeding in KMC position Vs supine position in preterm and low-Birth-weight newborns (less then 1500 g) In reducing feed intolerance: A randomized Control 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  Dipen Vasudev Patel 
Designation  Professor and Head of Department 
Affiliation  Shree Krishna Hospital, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand 
Address  Shree Krishna Hospital, Department of Neonatology, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand

Anand
GUJARAT
388325
India 
Phone  9825331453  
Fax    
Email  dipen_patel258@yahoo.co.in  
 
Details of Contact Person
Scientific Query
 
Name  Smit Jitendrakumar Shethwala 
Designation  1st Year DM Neonatology Resident 
Affiliation  Shree Krishna Hospital, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand 
Address  Shree Krishna Hospital, Department of Neonatology, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand

Anand
GUJARAT
388325
India 
Phone  7574870554  
Fax    
Email  smitshethwala@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dipen Vasudev Patel 
Designation  Professor and Head of Department 
Affiliation  Shree Krishna Hospital, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand 
Address  Shree Krishna Hospital, Department of Neonatology, Pramukhswami Medical College, Bhaikaka University, Karamsad, District- Anand

Anand
GUJARAT
388325
India 
Phone  9825331453  
Fax    
Email  dipen_patel258@yahoo.co.in  
 
Source of Monetary or Material Support  
Shree Krishna Hospital, Pramukhswami Medical College, Karamsad, Anand - 388325, Gujarat 
 
Primary Sponsor  
Name  Shree Krishna Hospital 
Address  Department of Neonatology, Pramukhswami Medical College, Bhaikaka University, Karamsad, Anand-388325, Gujarat, India 
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dipen Vasudev Patel  Shree Krishna Hospital  Room Number 253, Department and Division of Neonatology, Pramukhswami Medical College, Bhaikaka University, Karamsad
Anand
GUJARAT 
9825331453

dipen_patel258@yahoo.co.in 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee-2  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: P788||Other specified perinatal digestive system disorders,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Gavage feeding in KMC (Kangaroo Mother Care) position  Infants will receive slow Gavage feeding via syringe Pump over 1 h while in a semi-Upright, prone KMC position on The caregiver’s chest as many Times as possible 
Comparator Agent  Gavage feeding in Supine position  Infants will receive slow gavage Feeding via syringe pump over 1 Hour in a supine position Under a radiant warmer or on bed  
 
Inclusion Criteria  
Age From  1.00 Day(s)
Age To  3.00 Month(s)
Gender  Both 
Details  Preterm (Gestational age less then 37 weeks) and Low-Birth-Weight Newborns (Birth weight less then 1500 grams) eligible For KMC (Kangaroo Mother Care) And requiring gavage feeding will be Enrolled.  
 
ExclusionCriteria 
Details  1-Major congenital anomalies or genetic disorder
2-Birth asphyxia (Apgar less then 5 at 10 minutes Or blood Gas pH less then 7 or base excess more Then -16)
3-Intraventricular Haemorrhage Grade II or More (Volpe)
4-Hypotension requiring inotropes
5-Abnormal fetal Doppler indices.
6-NEC Stage II or more (Modified Bell’s Criteria) 
 
Method of Generating Random Sequence   Stratified randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
To compare the incidence of Feeding intolerance (defined By any of this: prefeed Gastric Residual Volume more Then 50 percents, abdominal Distension more then 2 cm, Regurgitation or vomiting, Occult or overt blood in Stool), between the two Groups.  Data will be collected until The infant starts accepting Oral feeding by spoon or Direct breastfeeding 
 
Secondary Outcome  
Outcome  TimePoints 
1-Number of Nil Per Mouth (NPO) days.
2-Episodes of bradycardia (Pulse Rate less then 100 / Min), desaturation (SPO2 less Then 85%), thermoregulation And other significant events.
3-To assess weight gain and length of hospital stay.
4-To compare total daily KMC Hours between groups.
5-To evaluate feasibility and Acceptability of GF KMC among Nurses and mothers. 
Data will be collected until The infant starts accepting Oral feeding by spoon or Direct breastfeeding 
 
Target Sample Size   Total Sample Size="150"
Sample Size from India="150" 
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)   10/01/2026 
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="2"
Months="0"
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
  1. What data in particular will be shared?
    Response - All of the individual participant data collected during the trial, after de-identification.

  2. What additional supporting information will be shared?
    Response -  Study Protocol
    Response -  Statistical Analysis Plan

  3. Who will be able to view these files?
    Response - Researchers whose proposed use of the data has been approved by an independent review committee identified for this purpose.

  4. For what types of analyses will this data be available?
    Response - To achieve aims in the approved proposal.

  5. By what mechanism will data be made available?
    Response - Proposals should be directed to [dipen_patel258@yahoo.co.in].

  6. For how long will this data be available start date provided 01-01-2029 and end date provided 31-12-2033?
    Response - Beginning 3 months and ending 5 years following article publication.

  7. Any URL or additional information regarding plan/policy for sharing IPD? 
    Additional Information - NIL
Brief Summary  

1.     Brief summary of intended work:

1.1   Need for the study: 

Feeding intolerance (FI) is a common problem among preterm / low-birth-weight (LBW) infants due to immature gastrointestinal function and increased susceptibility to complications such as necrotizing enterocolitis (NEC) [1]. The clinical definition of FI varies across studies, but it is commonly identified by increased gastric residuals, abdominal distension, and vomiting [2]. These complications delay the establishment of full enteral feeds, prolong parenteral nutrition, and adversely affect growth and clinical outcomes. 

Gavage feeding is frequently required in preterm / LBW infants who are unable to coordinate suck, swallow, and breathing reflexes and those who are seek [3]. During gavage feeding, milk is administered through a tube inserted orally or nasally into the stomach, typically while the infant lies supine in a crib or under a radiant warmer. Studies have explored various feeding techniques, including gravity-assisted, syringe pump-assisted, bolus, intermittent, and continuous methods; however, consensus on the optimal approach remains lacking. Feeding duration varies from 10 to 30 minutes or more, and both the rate of infusion and infant position may influence feeding tolerance through mechanisms such as altered gastric emptying, aspiration risk, or cardiorespiratory instability [4,5]. 

National and international guidelines endorse Kangaroo Mother Care (KMC) as a standard practice for stable LBW infants. KMC has been shown to enhance thermoregulation, breastfeeding outcomes, infection control, and mother–infant bonding [6]. Physiological proximity during KMC may also improve gastrointestinal motility and feeding tolerance compared with standard supine positioning [7]. However, despite KMC’s well-documented benefits, its integration into feeding routines remains limited, particularly in resource-constrained settings [8].

Our neonatal unit often practices syringe pump-assisted gavage feeding over one hour while infants are in the KMC position (GF KMC) . In KMC, the infant lies prone on the caregiver’s chest in skin-to-skin contact [9]. The World Health Organization recommends that gavage feeding can be safely provided during KMC [9]. Evidence suggests that prone positioning reduces gastric residuals, a surrogate marker for feeding tolerance, yet literature on feeding during KMC remains scarce [10].

Therefore, this study aims to compare Gavage Feeding in KMC position (GF KMC) versus Gavage Feeding in Supine position (GF Supine) to assess feeding intolerance among LBW infants.

1.2   Review of literature

Feeding intolerance is a frequent clinical concern in preterm infants, reflecting their inability to tolerate enteral nutrition. It manifests as increased gastric residual volumes (GRV), abdominal distension, vomiting, or blood in stool, leading to interruption of feeds. However, definitions and diagnostic criteria vary widely across studies, complicating interpretation and comparison [11]. Meta-analyses estimate the prevalence of FI between 15–30%, with a pooled rate of approximately 27%.

 Gavage feeding is essential in LBW infants who cannot coordinate oral feeding. Modes of delivery—intermittent bolus or continuous infusion—have distinct physiological effects. Studies show that slow intermittent feeding over one hour using a syringe pump enhances adult like- duodenal motor response, improves gastric emptying, stabilizes hormonal responses, and improves tolerance compared with rapid bolus or continuous methods [12,13]. Moreover, Continuous feeding results in less insulin and amino acid hormonal surges, which diminishes protein synthesis compared to intermittent bolus feeding [13].

 Atay et al. compared slow infusion intermittent feeding (SIF) using a syringe pump (1 hour) with gravity-fed intermittent bolus feeding (IBF) in preterm infants (24–31+6 weeks). The SIF group had significantly fewer FI episodes, shorter nil per oral (NPO) durations, and faster weight regain, highlighting the benefits of controlled, slow infusion feeding [14]. Similarly, Kumar V et al. found no major differences in time to full feeding or growth between continuous, intermittent infusion, and gravity bolus groups but emphasized that pump-assisted feeding ensures better timing control [15].

 Fanaro et al. on feeding intolerance highlights that slow infusion improves duodenal motility and gastric emptying in preterm infants, which physiological studies support. Slow feeding by pump reduces feeding intolerance incidences, which is crucial in LBW infants who often experience delayed gastric emptying and immature GI function [16]. This is congruent with the RCT findings by Atay et al. and Kumar et al., where controlled timing and slow delivery of feeds using infusion pumps reduced feeding intolerance relative to gravity bolus feeding approaches.

 Recent literature shows that KMC offers significant benefits for feeding tolerance in preterm infants by improving digestion, vital signs, and reducing symptoms such as gastric residual volume, vomiting, and abdominal distension, when compared to routine supine/prone positioning [9]. KMC significantly reduced episodes of FI compared to standard supine/prone care, with lower mean GRVs (KMC: 0.84 ± 3.28 ml vs. 4.17 ± 6.04 ml in supine/prone group) and fewer instances of abdominal distension or vomiting. FI was observed in only 4.8% of KMC infants versus 21.4% with standard care. But, in this study KMC was provided for 1 hour after the gavage feeding was over [17]. Continuing tube feeding while ongoing KMC has not been explored yet, however a preliminary study reported less feed intolerance with feeding the newborn prone in KMC position [7].

 In recently submitted thesis at Bhaikaka University on feed intolerance by Patel DV et al, on Gravity assisted ‘bolus’ feeding over 5-10 min versus syringe pump assisted ‘slow’ intermittent gavage feeding over 30 min in preterm newborns found superiority of syringe pump assisted ‘slow’ intermittent gavage feeding over 30 min in reducing feed intolerance (18). After this study and based on the benefits of 1 h slow feeding using syringe pump from other study, 1 h slow intermittent feeding is a norm in our Neonatal Intensive Care Unit (NICU) [14,18].

 To improve KMC hours, we often practice tube feeding (gavage feeding) in KMC position [9]. Prone position alone has been found to reduce feed intolerance in term of reduced GRV [10], but its use has been limited due to increased incidence of sudden infant death in isolated prone position [19], this is not the case in KMC position as KMC reduces neonatal mortality [9]. This study explores utility of KMC as a feeding position of newborn to assess incidence of feed intolerance.  

2   Material and method:

2.1  Source of data:

The study will be conducted in the NICU and KMC wards of Shree Krishna Hospital. Feeding practices follow national guidelines ICMR [20]. Infants unable to feed orally are given gavage feeds using syringe pumps over one hour under clinician supervision every 3 h interval, i.e. total eight times in 24 h. 

2.2  Methodology:

Design: Prospective, balanced and stratified parallel-group randomized controlled trial.

Randomization and Study Procedure:

Eligible newborns will be randomized (1:1) by balanced stratification [Birth weight, and Appropriate for Gestational Age (AGA)/ Small for Gestational Age (SGA)] to either GF KMC (intervention) or GF Supine (control) using Stata v 14.2. Allocation will be concealed using sequentially numbered, opaque, sealed envelopes maintained by a nurse not involved in data collection. The statistician will remain blinded to group assignments.

 In the control group, infants will receive slow gavage feeding via syringe pump over 1 h in a supine position under a radiant warmer or on bed at every 3 h interval. KMC will be practiced in this group at the time when the newborn is not receiving the gavage feeds.

 In the intervention group, infants will receive slow gavage feeding via syringe pump over 1 h while in a semi-upright, prone KMC position on the caregiver’s chest as many times as possible. During rest of the times (e.g. mother / caretaker is not available / resting), gavage feeding will be given in supine position.

 Study end points: Data will be collected until the infant starts accepting oral feeding by spoon or direct breastfeeding. Changes in feeding mode by the clinician will also be considered an endpoint. At the end point, a feasibility survey of mothers (in GF KMC group) and nurses will be carried out by the investigators. The questions in the survey are Yes/ No type and open ended.

 Baseline perinatal characteristics (gestational age, birth weight, sex, delivery mode, SGA status, Apgar scores, etc.) will be documented for both groups.

 
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