Clinical Trial

Diaphragm Dysfunction and Ultrasound Perioperatively

Study acronym: DiaphPeriop
Recruiting
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Summary
This study aims at determining whether diaphragm ultrasound examining diaphragm thickening fraction, excursion and density before and after surgery can predict respiratory complications in the postoperative period. Patients scheduled for major elective abdominal, pelvic or vascular surgery will be included in the study and diaphragm ultrasound is performed before surgery and after surgery in the postoperative ward. Physiological parameters, laboratory parameters, data on surgery and anesthesia and comorbidities will be registered. Complications such as pneumonia, desaturation, need for intubation and other respiratory events up to 30 days will be registered and later correlated with the diaphragm measurements.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2023-06-07.
Status change: Not Yet Recruiting → Recruiting 2025-01-27
Trial Details
NCT Number NCT05906030
Lead Sponsor Karolinska University Hospital
Collaborators: Karolinska Institutet
Conditions Respiratory Insufficiency, Pneumonia, Desaturation of Blood, Tachypnea, Atelectasis, Postoperative
Enrollment 160 participants
Start Date 2024-09-01
Primary Completion 2026-09-01 (estimated)
Study Completion 2027-09-01 (estimated)
Updated on ClinicalTrials.gov 2025-01-29