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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01890564
Other study ID # IRB12-00783
Secondary ID
Status Completed
Phase N/A
First received June 27, 2013
Last updated March 31, 2014
Start date June 2013
Est. completion date January 2014

Study information

Verified date March 2014
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

During minimally invasive surgery, a pneumoperitoneum is created to facilitate surgical visualization. Although effective in facilitating the procedure, there are respiratory consequences of the pneumoperitoneum, which significantly increases intra-abdominal pressure (IAP) up to 20 cmH2O. The increased IAP can decrease functional residual capacity and increase closing capacity resulting in increased resistance, decreased compliance, and increased ventilation-perfusion mismatch. In a randomized, cross-over design, this study will evaluate in sequential order, 3 modes of ventilation during laparoscopic bariatric surgery to determine which is better able to support oxygenation and ventilation while limiting the peak inflating pressure (PIP).


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Both
Age group 14 Years to 20 Years
Eligibility Inclusion Criteria:

- Laparoscopic bariatric surgery requiring intra-arterial blood pressure monitoring, age 14-20 years.

Exclusion Criteria:

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Pressure controlled ventilation
For pressure controlled ventilation, the peak inflating pressure (PIP) is set for each tidal breath.
Volume controlled ventilation
For volume controlled ventilation, the tidal volume is set.
PRVC ventilation
Pressure-regulated, volume-controlled (PRVC) is an auto-regulated pressure-controlled mode of mechanical ventilation with a user-selected tidal volume target.

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
Joseph D. Tobias

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in heart rate Heart rate will be assessed every 5 mins. during each 30 minute mode of ventilation. Baseline to 30 mins. No
Secondary Change in blood pressure Blood pressure will be recorded every 5 mins. during each 30 minute mode of ventilation. Baseline to 30 mins. No
Secondary Blood gas Blood gas will be obtained at the end of each 30 minute mode of ventilation. 30 mins. No
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