The Efficacy and Mechanisms of Oral Probiotics in Preventing Necrotizing Enterocolitis

NCT02552706 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2016-03-29

No results posted yet for this study

Summary

The purpose of this study is to investigate the efficacy and its mechanisms of oral mixture probiotics in preventing necrotizing enterocolitis among the preterm very low birth weight infants.

Conditions

  • Necrotizing Enterocolitis
  • Death

Interventions

DIETARY_SUPPLEMENT

probiotics

Administration of mixture probiotics 500mg by mouth, one time or divided into 2-4 times depends on the feeding volume until to 36 weeks post menstrual age.

DIETARY_SUPPLEMENT

glucose solution

Administration of 1 mL of a 5% glucose solution by mouth, one time or divided into 2-4 times depends on the feeding volume until to 36 weeks post menstrual age.

Sponsors & Collaborators

  • China Medical University Hospital

    collaborator OTHER
  • Shenzhen People's Hospital

    collaborator OTHER
  • Shenzhen Sixth People's Hospital

    collaborator OTHER
  • Longhua Hospital Of Baoan District, Shenzhen

    collaborator OTHER
  • Shenzhen Bao'an Maternal and Child Health Hospital

    lead OTHER

Principal Investigators

  • Yuefeng Li, M.D. · Shenzhen Bao'an Maternal and Child Health Hospital

  • HungChih Lin, M.D. · China Medical University Hospital

  • Benqing Wu, M.D. · Shenzhen People's Hospital

  • Xiaodong Li, M.D. · Shenzhen Sixth People's Hospital

  • Zhangxin Wang, M.D. · Longhua Hospital Of Baoan District, Shenzhen

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Max Age
3 Days
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2017-01-31
Completion
2017-09-30

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02552706 on ClinicalTrials.gov