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NCT03214744 Clinical Trial

Rapid Versus Slow Entral Feeding Advancements on Clinical Outcomes of Preterm Infants

Preterm Infant Clinical Trial

— pretermfood  

Official title:
Rapid Versus Slow Entral Feeding Advancements on Clinical Outcomes of Preterm Infants

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03214744
Other study ID # 17100036
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 9, 2017
Last updated July 12, 2017
Start date May 2018
Est. completion date June 2019

Study information
Verified date July 2017
Source Assiut University
Contact professor Mohamed Mahrous Sayed
Phone 01003486595
Email Eltellawy270@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Rapid Versus Slow Entral Feeding Advancements on Clinical Outcomes of Preterm Infants

Description:

Rapid feeding advancement achieves full enteral volume of feedings earlier than the slower advancement.They received significantly fewer days of parenteral nutrition, exhibited a shorter time to regain birth weight and shorter duration of hospital stay. The incidence of NEC and the number of episodes of feeding intolerance were not significantly different between rapid and slow advancement. while the incidence of culture-proven late onset sepsis was significantly less in infants receiving a rapid feeding advancement

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 1
Est. completion date June 2019
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group N/A to 15 Weeks
Eligibility Inclusion Criteria:

- All preterm neonates admitted to NICU with gestational age less than 36 weeks, and haemodynamically stable

Exclusion Criteria:

- gastrointestinal tract anomalies,

- haemodynamically unstable infants,

- gestatinal age equal or more than 36 weeks,

- preterms who develop NEC,

- preterms on mechanical ventilation.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Egypt Assiut university Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Pike K, Brocklehurst P, Jones D, Kenyon S, Salt A, Taylor D, Marlow N. Outcomes at 7 years for babies who developed neonatal necrotising enterocolitis: the ORACLE Children Study. Arch Dis Child Fetal Neonatal Ed. 2012 Sep;97(5):F318-22. doi: 10.1136/fetalneonatal-2011-300244. Erratum in: Arch Dis Child Fetal Neonatal Ed. 2013 Sep;98(5):e1. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary effect of entral feeding on preterm -Length of hospital stay. six months
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