6246032
Last Update Posted: 2024-02-07
Recruiting has ended
All Genders accepted | Under 2 months |
30 Estimated Participants | No Expanded Access |
Interventional Study | Does not accept healthy volunteers |
Impact of Modified Feeding Protocol on Neonatal Outcomes
The goal of this clinical trial is to compare modified feeding protocol and current feeding protocol on neonatal outcomes in preterm infants who born with weight less than 2kg.
The main questions it aims to answer are:
- Is Modified feeding protocol will decrease the duration of parenteral nutrition and length of hospital stay?
- Is Modified feeding protocol feasible, efficient, and safe in preterm infants?
Participants will undergo the modified feeding protocol since birth until discharge.
two group in this study Prospective group: intervention group will undergo the modified feeding protocol Retrospective group: intervention group will undergo the current feeding protocol
Both group will have care as routine care to this kind of patients But the differ will be in feeding protocol as initiation rate, advancement rate, human milk fortification rate
The outcomes of both group will be compeered to meet the study objectives
Eligibility
Relevant conditions:
Preterm
Birth Weight
Feeding Disorder Neonatal
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
Inclusion criteria
Exclusion criteria
locations
Contact Information
Overall Contact
No valid contacts available
Data sourced from ClinicalTrials.gov