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NCT00665405 Clinical Trial

Atelectasis During Delivery - Comparing Cesarian (c) -Section and Labor

Cesarean Section Clinical Trial

Official title:
CT Study of Atelectasis After Delivery - Comparison Between Cesarian Section and Labor

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00665405
Other study ID # CAP649-05
Secondary ID
Status Completed
Phase N/A
First received April 21, 2008
Last updated April 21, 2008
Start date July 2006
Est. completion date November 2007

Study information
Verified date January 2008
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Observational

Clinical Trial Summary

Pregnancy promotes respiratory system's restrictive component. This study observes the generation of atelectasis during labor.

Description:

Pregnancy causes restriction of diaphragm movements as well as higher resistive component to the respiratory system. Spirometry studies have shown that the supine position increases risks of hypoxemia. There seems to be only casual observation regarding the generation of atelectasis during labor.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date November 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- post-anesthesia recovery

Exclusion Criteria:

- hemodynamic disorder during labor

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Radiation:
• CT scan
Thoracic CT scan

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Sao Paulo

Outcome
Type Measure Description Time frame Safety issue
Primary atelectasis 60-120 minutes after delivery No
See also
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Recruiting NCT06247852 - Persistent Pain After Cesarean Delivery - A Danish Multicenter Cohort Study
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