Diaphragm Dysfunction and Ultrasound Perioperatively

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorKarolinska University Hospital

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

<18 years

Underlying chronic respiratory disease

Patients not able to give informed consent

Trial design

Treatments tested in this trial

  • Diaphragm ultrasound

Treatment groups

No treatment groups listed

Sponsors and collaborators

Karolinska University Hospital

Lead sponsor

Karolinska Institutet

Collaborator