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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02622152
Other study ID # IRB0000871200
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 30, 2016
Est. completion date December 2018

Study information

Verified date July 2018
Source Assiut University
Contact sayed abd-elshafy, MD
Phone 0020882413203
Email sayed_k_72@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Directly following cardiac surgery for congenital heart disease; patients are not receiving routine turning every two hours to prevent pressure ulcers, because a negative influence on hemodynamic parameters is assumed. Investigators have suggested that lateral position may have clinically significant effects on oxygenation in cardiac surgery patients.


Description:

Sixty pediatric congenital heart disease patients were randomly assigned to two equal intervention groups


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender All
Age group 1 Year to 10 Years
Eligibility Inclusion Criteria:

- Age within 10 years with a cyanotic congenital heart disease

- Hemodynamic stability with no compromising arrhythmia

- No respiratory arrest

- Not connected with mechanical ventilation

Exclusion Criteria:

- Cyanotic congenital heart disease

- Hemodynamic instability

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Right lateral position (2 hours)
Repositioning the patients for two-hours period on the right lateral position
Left lateral position (30 minutes)
Repositioning the patients for 30 minutes period on the left lateral position
Supine position (30 minutes)
Repositioning the patients for 30 minutes period on the supine position
Left lateral position (2 hours)
Repositioning the patients for two-hours period on the left lateral position
Supine position (2 hours)
Repositioning the patients for two-hours period on supine position

Locations

Country Name City State
Egypt Faculty of Medicine Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Arterial oxygenation The samples will be analyzed by a blood gas analyzer before and after changing position Duration of Intensive Care Unit Admission after weaning from mechanical ventilation an expected average of 4 days
Secondary Blood pressure Systolic, diastolic and mean blood pressure " mm Hg" Duration of Intensive Care Unit Admission after weaning from mechanical ventilation an expected average of 4 days
Secondary Heart rate Heart rate "beats per minute" Duration of Intensive Care Unit Admission after weaning from mechanical ventilation an expected average of 4 days
Secondary Oxygen saturation Oxygen saturation % Duration of Intensive Care Unit Admission after weaning from mechanical ventilation an expected average of 4 days
Secondary Respiratory rate Respiratory rate "rate per minute" Duration of Intensive Care Unit Admission after weaning from mechanical ventilation an expected average of 4 days
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