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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04168151
Other study ID # 68
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date October 10, 2020

Study information

Verified date January 2021
Source University of Alexandria
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the study is conducted on hypoxic adult patients underwent open heart surgery after arrival to the intensive care unit and stabilization of patients' hemodynamics to assess the efficacy of transalveolar pressure measurement as an index for lung recruitment.


Description:

After one hour from the patient's ICU admission and after stabilization of the patient's haemodynamics, alveolar recruitment will be done for hypoxic patients with hypoxic index less than 250. The recruitment will be started in the adaptive ventilation mode (AVM mode) using modified stepwise staircase recruitment maneuver in which every 2 minutes positive end-expiratory pressure (PEEP) is increased in increments of 2 cmH2O and the driving pressure will be regulated by AVM mode. The increase in PEEP will be guided by improvement of dynamic compliance, oxygen saturation and transalveolar pressure (PTA) till near overdistention. Overdistension will be detected if there are decrease in the mean arterial pressure 25% from the base line value reported after stabilization of the patient's haemodynamics, or decreased oxygen saturation or sudden decrease in dynamic compliance, or inspiratory PTA more than15 cm H2O. Then PEEP is decreased 2 cm H2O every 3 minutes till a decrease expiratory PTA less than 1 cm H2O, or a decrease in dynamic compliance or a decrease in oxygen saturation ≥ 1% from maximum oxygen saturation is observed (the derecruitment point) then return to a PEEP level 2 cm H2O above the derecruitment point (the optimal PEEP). Alveolar recruitment will be done once.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date October 10, 2020
Est. primary completion date October 10, 2020
Accepts healthy volunteers No
Gender All
Age group 19 Years to 75 Years
Eligibility Inclusion Criteria: - post cardiac surgery hypoxic adult patients Exclusion Criteria: 1. Patients with contraindications for the use of esophageal catheter including esophageal ulcerations, tumors, diverticulitis, bleeding varices, recent esophageal or gastric surgery, sinusitis, epistaxis and recent nasopharyngeal surgery. 2. Postoperative severe haemodynamic instability on high inotropic support. 3. Ejection fraction less than 35%. 4. Severe restrictive or obstructive lung disease. 5. Extremes of age (<19 and > 75 years). 6. Morbid obese patients with BMI > 40kg/m2.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
lung recruitment protocol
lung recruitment protocol applied to postcardiac surgery hypoxic adult patients with measurement of trans alveolar pressure as an index for lung recruitment

Locations

Country Name City State
Egypt Alexandria main university hospital Alexandria

Sponsors (1)

Lead Sponsor Collaborator
University of Alexandria

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary transalveolar pressure cmH2O 1 day
Primary hypoxic index 1 day
Secondary dynamic compliance ml/cmH2O 1 day
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