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Parasternal Intercostal Muscle Thickening as an Additive Weaning Criterion

Parasternal Intercostal Muscle Thickening as an Additive Weaning Criterion to Minimize Re-intubation Rate: a Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07143695
Enrollment
200
Registered
2025-08-27
Start date
2025-09-01
Completion date
2026-08-31
Last updated
2025-09-08

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

Conditions

Critically Ill

Keywords

Weaning, re-intubation, mechanical ventilation

Brief summary

Increased days of MV are not without hazards, including barotraumas and ventilator-associated pneumonia. Similarly, premature separation of MV is associated with increased mortality secondary to adverse cardiorespiratory events. Therefore, the time of weaning should be wisely evaluated. There is growing evidence concerning respiratory muscles dysfunction that contributes to difficulty or prolonged liberation from MV.

Detailed description

Researchers aim to evaluate the influence of adding parasternal thickening fraction to the standard weaning criteria and its impact on reintubation

Interventions

DEVICEParasternal intercostal thickening fraction

Parasternal intercostal thickening fraction less than 6.5%

DEVICESham parasternal intercostal thickening

Ultrasound assessment only for purpose of blinding

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* critically ill patient mechanically ventilated for 24 hours or more first spontaneous breathing trial

Exclusion criteria

* patient refusal difficult ultrasound views tracheostomized patient neuromuscular disorders

Design outcomes

Primary

MeasureTime frameDescription
Incidence of reintubationWithin 72 hours after extubationneed for reintubation

Secondary

MeasureTime frameDescription
Incidence of weaning failurewithin 72 hours post-extubationfailed spontaneous breathing trial or reintubation

Countries

Egypt

Contacts

Primary ContactCairo university
kasralainirec@gmail.com+201275716942

Outcome results

None listed

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