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Effect of Thoracic Block Technique on Atelectasis in Children on Mechanical Ventilation

Effect of Thoracic Block Technique on Atelectasis in Children on Mechanical Ventilation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05480202
Enrollment
40
Registered
2022-07-29
Start date
2021-12-06
Completion date
2022-07-20
Last updated
2022-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atelectasis, Children, Intensive Care Unit

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.

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

Interventions

Manual compression of the healthy lung during expiration associated with the use of invasive or non invasive mechanical ventilation

Percussion, vibration and postural drainage

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
6 Months to 4 Years
Healthy volunteers
No

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 were excluded from the study if they had one of the following:

Design outcomes

Primary

MeasureTime frameDescription
Assessment of heart rate and respiratory rate10 days for each participantAssessment of change in heart rate and respiratory rate will be carried out by using electro cardiograph electrodes and pulse oximeter.
Assessment of atelectasis in chest x ray10 days for each participantAssessment of atelectasis in chest x ray will be carried out by comparing presence, extent and distribution of atelectasis in x ray film before and intervention
Assessment of arterial blood gases test10 days for each participantAssessment of change in arterial blood gases test will be carried out by comparing results before and after intervention

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026