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NCT03540940 Clinical Trial

PEEP During Induction of Anesthesia in Small Children

Pediatric Anesthesia Clinical Trial

Official title:
The Effect of Positive End-expiratory Pressure During Induction of General Anesthesia on Atelectasis Formation and Non-hypoxic Apnea Time in Small Children: a Randomized Controlled Trials

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03540940
Other study ID # H 1804-100-938
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 21, 2018
Est. completion date August 14, 2019

Study information
Verified date August 2019
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Positive end-expiratory pressure (PEEP) applied during induction of anesthesia prevents atelectasis formation and increases the duration of nonhypoxic apnea in obese and nonobese patients. PEEP also prevents atelectasis formation in pediatric patients. Because pediatric patients arterial desaturation during induction of anesthesia develops rapidly, we studied the clinical benefit of PEEP applied during anesthesia induction.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date August 14, 2019
Est. primary completion date August 14, 2019
Accepts healthy volunteers No
Gender All
Age group 1 Month to 2 Years
Eligibility Inclusion Criteria:

- pediatric patients undergoing general anesthesia using endotracheal intubation

Exclusion Criteria:

- previous history of lung disease

- anticipated difficulty in airway management

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• PEEP
7cmH2O positive end expiratory pressure
• ZEEP
0 cmH2O positive end expiratory pressure

Locations
Country Name City State
Korea, Republic of Hee-Soo Kim Seoul Soul-t'ukpyolsi
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Duration of Apnea from the start of apnea until SpO2 reached 95%, maximum 5 minutes.
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