Cerebral Near Infrared Spectroscopy During Blood Sampling From a Peripheral Artery Catheter in Preterm Infants

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2009 by University of Cologne.
Recruitment status was  Recruiting
Information provided by:
University of Cologne
ClinicalTrials.gov Identifier:
First received: June 23, 2009
Last updated: NA
Last verified: June 2009
History: No changes posted
Preterm infants often need peripheral artery catheters for invasive blood pressure recording and to facilitate blood sampling. Near infrared spectroscopy is a method to evaluate cerebral oxygenation and as well as cerebral blood flow. Sampling procedures with identical sampling volumes are performed at a short (40 seconds) and a long (70 seconds) time intervall while changes of cerebral oxygenation are measured. The investigators hypothesise that slower sampling decrease changes in cerebral blood flow.

Cerebral Oxygenation
Cerebral Blood Flow

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Measurement of Cerebral Oxygenation With Near Infrared Spectroscopy During Blood Sampling From a Peripheral Artery Catheter in Preterm Infants With Gestational Age <37+0

Further study details as provided by University of Cologne:

Estimated Enrollment: 20
Study Start Date: November 2008
Pretem infants (GG < 37+0)


Ages Eligible for Study:   up to 7 Days
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Preterm infants (Gestational Age <37+0)

Inclusion Criteria:

  • Preterm infant (Gestational Age <37+0)
  • Peripheral arterial catheter (ulnary or radial artery)

Exclusion Criteria:

  • Complex organ malformation
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00926770

University of Cologne, NICU Recruiting
Cologne, NRW, Germany, 50931
Contact: Angela Kribs, MD    0049221478 ext 5998    Angela.Kribs@uk-koeln.de   
Principal Investigator: Angela Kribs, MD         
Sub-Investigator: Katrin Mehler, MD         
Sponsors and Collaborators
University of Cologne
  More Information

No publications provided

Responsible Party: University of Cologne, Angela Kribs
ClinicalTrials.gov Identifier: NCT00926770     History of Changes
Other Study ID Numbers: 06-131 
Study First Received: June 23, 2009
Last Updated: June 23, 2009
Health Authority: Germany: Ethics Commission

ClinicalTrials.gov processed this record on February 07, 2016