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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01665287
Other study ID # 300712FORVOS
Secondary ID
Status Completed
Phase N/A
First received August 13, 2012
Last updated January 14, 2013
Start date August 2012
Est. completion date November 2012

Study information

Verified date January 2013
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research EthicsDenmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

Regional tissue oxygenation (rStO2) can be monitored by near infrared spectroscopy. The commercial devices FORE-SIGHT (CASMED) and INVOS (COVIDIEN) will be used simultaneously to test for their relative sensitivity for low oxygen levels just after birth on term infants born by elective cesarean section. Reproducibility will be examined by replacements of the sensors six times the next day when the infant is stable and quiet. Neonatal sensors will be used.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date November 2012
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A to 2 Minutes
Eligibility Inclusion Criteria:

- Term infants (age more than 37 weeks of gestation)

- Elective cesarean section after an uncomplicated pregnancy

Exclusion criteria:

- Thick hair that makes good measurements difficult/impossible

- Obvious malformations or syndrome

- Complications in relation to the cesarean section

- Depression after birth (APGAR < 8 after 1 minute)

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Department of Neonatology, Rigshospitalet Copenhagen

Sponsors (2)

Lead Sponsor Collaborator
Rigshospitalet, Denmark The Augustinus Foundation, Denmark.

Country where clinical trial is conducted

Denmark, 

References & Publications (4)

Kratky E, Pichler G, Rehak T, Avian A, Pocivalnik M, Müller W, Urlesberger B. Regional cerebral oxygen saturation in newborn infants in the first 15 min of life after vaginal delivery. Physiol Meas. 2012 Jan;33(1):95-102. doi: 10.1088/0967-3334/33/1/95. — View Citation

Noori S, Wlodaver A, Gottipati V, McCoy M, Schultz D, Escobedo M. Transitional changes in cardiac and cerebral hemodynamics in term neonates at birth. J Pediatr. 2012 Jun;160(6):943-8. doi: 10.1016/j.jpeds.2011.12.008. Epub 2012 Jan 11. — View Citation

Urlesberger B, Grossauer K, Pocivalnik M, Avian A, Müller W, Pichler G. Regional oxygen saturation of the brain and peripheral tissue during birth transition of term infants. J Pediatr. 2010 Nov;157(5):740-4. doi: 10.1016/j.jpeds.2010.05.013. Epub 2010 Jun 17. — View Citation

Urlesberger B, Kratky E, Rehak T, Pocivalnik M, Avian A, Czihak J, Müller W, Pichler G. Regional oxygen saturation of the brain during birth transition of term infants: comparison between elective cesarean and vaginal deliveries. J Pediatr. 2011 Sep;159(3):404-8. doi: 10.1016/j.jpeds.2011.02.030. Epub 2011 Apr 9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cerebral oxygenation The sensors of both instruments will be placed on each side of the head. They will be held by hand or by self-adhesive tape as appropriate.
Curve fitting will be used to describe the rapid increase of oxygenation after birth. Estimated cerebral oxygenation at 3 min (hypoxia) and 10 min (normoxia) will be used to compare the two instruments.
10 minutes No
Secondary Reproducibility The sensor will be placed 6 times alternating on each frontoparietal region and held by hand, obtaining 30 seconds of signal for each placement. The placements will be in the same region but not in exactly the same spot. This will be done for both devices. 10 minutes No
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