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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04626180
Other study ID # FUI/CTR/2020/7
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date June 1, 2018

Study information

Verified date September 2020
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Post operative pulmonary complication (PPC) is one of the cause of mortality and morbidity after sternotomy. There is no accessible confirmation which shows the impact of Pre Extubation Manual Hyperinflation method with Regular Extubation procedure. After sternotomy manual hyperinflation technique is not taken during extubation. The objective of the study was to determine the effect of Pre Extubation Manual Hyperinflation technique VS regular Extubation technique on vitals and respiratory parameters in patients after Sternotomy.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date June 1, 2018
Est. primary completion date February 1, 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: 1. Age 40 to 60 2. Patient undergone surgery (sternotomy) 3. Elective intubated (ETT orally) 4. Ventilated more than 3 hours - Exclusion Criteria: 1. Patient with any neurological issue (mentally disturbed) who cannot understand the command 2. Complicated extubation 3. Pulmonary pathology where lung hyperinflation was contra-indicated (e.g. acute respiratory distress syndrome, undrained pneumothorax or exacerbation of chronic obstructive pulmonary disease and acute pulmonary edema. 4. Raised intracranial pressure 5. Redo or reopen. -

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Extubation
Extubation is the removal of an endotracheal tube (ETT), which is the last step in liberating a patient from the mechanical ventilator.
Manual Hyperinflation
Providing a larger tidal volume than baseline tidal volume to the patient and using a tidal volume which is 50% greater than that delivered by the ventilator

Locations

Country Name City State
Pakistan Bahria International Hospital Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak expiratory flow rate 1 day
Primary Blood pH 1 day
Primary Blood pO2 1 day
Primary Blood pCO2 1 day
Primary Blood pHCO3 1 day
Primary Pulse rate 1 day
Primary Oxygen saturation 1 day
Primary Forced expiratory volume 1 day
Primary Forced vital capacity 1 day
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