MedTrace Logo

Effect of Implementing Cough Augmentation Techniques on Weaning Outcomes Among Critically Ill Patients

NCT07722260 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 88

Last updated 2026-07-23

No results posted yet for this study

Summary

The study aims to determine the effect of implementing cough augmentation techniques on weaning outcomes among critically ill patients

Conditions

  • Physiological Parameters

Interventions

OTHER

cough augmentation techniques

the lung volume recruitment maneuver via MV was applied with assistant of the attended physician as follows: Use pressure-controlled ventilation and increase end-inspiratory volume (30 or 40 cm H2O for 30 to 40 seconds unless contraindicated) or inspiratory hold for 30 to 40 seconds to promote cough effectiveness. The patient serially inhales a volume of gas without exhalation until maximum insufflation capacity via the ventilator to facilitate breath-holding (if not contraindicated).

Sponsors & Collaborators

Principal Investigators

  • sahar youness, professor · professor of critical care and emergency nursing

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-08
Primary Completion
2026-10-08
Completion
2026-11-10

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07722260 on ClinicalTrials.gov