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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00603837
Other study ID # 13223
Secondary ID
Status Completed
Phase N/A
First received December 19, 2007
Last updated October 12, 2009
Start date May 2007
Est. completion date November 2008

Study information

Verified date October 2009
Source University of Oklahoma
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Mean axillary temperatures, taken during NICU resuscitation upon admission to the NICU, will not differ between VLBW babies who are occlusively wrapped and very low birth weight (VLBW) babies who are placed on thermal warming blankets.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date November 2008
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 24 Weeks to 28 Weeks
Eligibility Inclusion Criteria:

- Participants in this study will be selected from the inborn population at University Hospital. Eligible patients will be selected from the group of babies with estimated gestational ages of 24-28 weeks and <1250g.

Exclusion Criteria:

- Congenital anomalies with open lesions such as meningomyelocele, or omphaloceles

- Blistering skin conditions

- Resuscitation not performed secondary to infant being below limits of viability as assessed by the in-house attending physician (specifically, according to current NRP recommendations):

- Where gestation, birth weight, and/or congenital anomalies are associated with almost certain early death, and unacceptably high morbidity is likely among the rare survivors, resuscitation is not indicated. Exceptions may be made based on parental desires.

- Newborns with confirmed gestation age of less than 24 weeks or birth weight less than 400 grams

- Anencephaly

- Confirmed Trisomy 13 or Trisomy 18 syndrome

- Meconium staining of amniotic fluid

- Birth assessment of gestational age > 28 weeks or >1250 grams

- Maternal temp >38 degrees C around the time of delivery.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
NeoWrap
This is a polyethylene wrap that will be placed around the ELGAN from the neck down to prevent heat loss.
InfaTherm
A gel blanket containing a sodium acetate-based medium that, when activated, becomes exothermic and provides heat.

Locations

Country Name City State
United States Oklahoma University Health Sciences Center Oklahoma City Oklahoma

Sponsors (1)

Lead Sponsor Collaborator
University of Oklahoma

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neonatal Intensive Care Unit (NICU) Admission Temperature At time of admission to the NICU - usually within 10-15 min of birth Yes
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