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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03823716
Other study ID # IRB17-00032
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2017
Est. completion date November 8, 2019

Study information

Verified date February 2020
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In order to evaluate current anesthetic practice in the care of preterm infants and neonates, the investigators will retrospectively review surgical procedures in infants who are less than 60 weeks post-conceptual age in which an arterial cannula was placed intraoperatively or in situ upon arrival in the operating room. They will evaluate the mode of ventilation (pressure or volume-controlled), tidal volume or peak inflating pressure, the level of PEEP, inspired oxygen concentration (FiO2), and respiratory rate used during the procedure to determine the average minute ventilation.


Recruitment information / eligibility

Status Completed
Enrollment 112
Est. completion date November 8, 2019
Est. primary completion date November 8, 2019
Accepts healthy volunteers No
Gender All
Age group N/A to 36 Weeks
Eligibility Inclusion Criteria:

- neonates (<60 weeks post-conceptual age) undergoing non-cardiac operative procedures in which arterial access is generally present (exploratory laparotomy or thoracotomy)

Exclusion Criteria:

- none

Study Design


Locations

Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Nationwide Children's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Decreased Partial Pressure of Carbon Dioxide (PaCO2) PaCO2 from arterial blood gas (ABG) = 35 During surgical procedure (average of 2-3 hours)
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