Incubator Weaning of Moderately Preterm Infants
NCT02160002 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 366
Last updated 2019-03-22
Summary
The objective of this proposal is to evaluate whether weaning from an incubator to a crib at lower versus higher weight, 1600g or 1800g will result in shorter length of hospital stay among moderately preterm infants.
The hypothesis of this study is that length of hospital stay (from birth to discharge) will be decreased among moderate preterm infants weaned from an incubator to an open crib at a lower versus higher weight, 1600g vs. 1800g.
Conditions
- Infant, Newborn
- Infant, Moderate Preterm
Interventions
- PROCEDURE
-
Weaning from an incubator at a lower weight (1600 grams)
Infants will be weaned from an incubator at a lower weight (1600 grams)
- PROCEDURE
-
Weaning from an incubator at a higher weight (1800 grams)
Infants will be weaned from an incubator at a higher weight (1800 grams)
Sponsors & Collaborators
-
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
collaborator NIH -
NICHD Neonatal Research Network
lead NETWORK
Principal Investigators
-
Michele C Walsh, MD · Case Western Reserve University, Rainbow Babies and Children's Hospital
-
Myra Wyckoff, MD · University of Texas, Southwestern Medical Center at Dallas
-
Seetha Shankaran, MD · Wayne State University
-
David Carlton, MD · Emory University
-
Kurt Schibler, MD · Children's Hospital Medical Center, Cincinnati
-
Brenda B Poindexter, MD · Indiana University
-
Abbot Laptook, MD · Brown University, Women & Infants Hosptial of Rhode Island
-
Krisa P Van Meurs, MD · Stanford University
-
Waldemar Carlo, MD · University of Alabama at Birmingham
-
Kathleen A Kennedy, MD · The University of Texas Health Science Center, Houston
-
Mike Cotten, MD · Duke University
-
Edward F Bell, MD · University of Iowa
-
Kristi Watterberg, MD · University of New Mexico
-
Barbara Schmidt, MD · University of Pennsylvania
-
Carl T D'Angio, MD · University of Rochester
-
Uday Devaskar, MD · University of California, Los Angeles
-
Pablo Sanchez, MD · Research Institute at Nationwide Children's Hospital
-
William Truog, MD · Children's Mercy Hospital Kansas City
-
Abhik Das, PhD · RTI International
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 29 Weeks
- Max Age
- 34 Weeks
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-02-28
- Primary Completion
- 2016-07-31
- Completion
- 2017-06-30
Countries
- United States
Study Locations
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