Ignite Creation Date:
2025-12-25 @ 4:05 AM
Ignite Modification Date:
2025-12-26 @ 3:01 AM
Study NCT ID:
NCT05480202
Status:
COMPLETED
Last Update Posted:
2022-07-29
First Post:
2022-07-26
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Effect of Thoracic Block Technique on Atelectasis in Children on Mechanical Ventilation
Sponsor:
Cairo University
Organization:
Study Overview
Official Title:
Effect of Thoracic Block Technique on Atelectasis in Children on Mechanical Ventilation
Status:
COMPLETED
Status Verified Date:
2022-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Statement of the problem:
• Does the thoracic block technique has effect on atelectasis in Children on Mechanical Ventilation?
Null hypothesis:
• there is effect of thoracic block technique on atelectasis in children on Mechanical ventilation.
• Does the thoracic block technique has effect on atelectasis in Children on Mechanical Ventilation?
Null hypothesis:
• there is effect of thoracic block technique on atelectasis in children on Mechanical ventilation.
Detailed Description:
Subjects:
The study targets the children from both sexes. Sample size estimation will be carried out to determine the recruited number of children, selected randomly from Cairo University pediatric specialized hospital intensive care units ,Cairo to participate in the study
Study design:
Randomized controlled clinical trial.
A. Inclusion criteria:
1. age range from 6 months to 4 years .
2. diagnosed with pneumonia, receiving Mechanical ventilation.
3. start from second day of admission to intensive care unit.
4. have unilateral mild to moderate atelectasis according to medical referral .
5. should be vitally stable during the session.
B. Exclusion criteria:
The children will be excluded from the study if they had one of the following:
1. medically unstable ( examples: tachycardia and tachypnea).
2. uncontrolled convulsion.
3. irritable or moderate to sever pain
4. rib fracture
5. pneumothorax
Children will be assessed by measuring heart rate, respiratory rate, chest x-ray, arterial blood gases,dynamic compliance, oxygen saturation index before and after ten days of receiving intervention
The study targets the children from both sexes. Sample size estimation will be carried out to determine the recruited number of children, selected randomly from Cairo University pediatric specialized hospital intensive care units ,Cairo to participate in the study
Study design:
Randomized controlled clinical trial.
A. Inclusion criteria:
1. age range from 6 months to 4 years .
2. diagnosed with pneumonia, receiving Mechanical ventilation.
3. start from second day of admission to intensive care unit.
4. have unilateral mild to moderate atelectasis according to medical referral .
5. should be vitally stable during the session.
B. Exclusion criteria:
The children will be excluded from the study if they had one of the following:
1. medically unstable ( examples: tachycardia and tachypnea).
2. uncontrolled convulsion.
3. irritable or moderate to sever pain
4. rib fracture
5. pneumothorax
Children will be assessed by measuring heart rate, respiratory rate, chest x-ray, arterial blood gases,dynamic compliance, oxygen saturation index before and after ten days of receiving intervention
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: