Diaphragm Dysfunction and Ultrasound Perioperatively

NCT05906030 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 160

Last updated 2025-01-29

No results posted yet for this study

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.

Conditions

  • Respiratory Insufficiency
  • Pneumonia
  • Desaturation of Blood
  • Tachypnea
  • Atelectasis, Postoperative

Interventions

DIAGNOSTIC_TEST

Diaphragm ultrasound

Diaphragm ultrasound will be used pre- and postoperatively. Diaphragm dysfunction will be diagnosed using the measurements diaphragm thickening fraction, diaphragm excursion and diaphragm density.

Sponsors & Collaborators

Principal Investigators

  • Jessica Kåhlin · Karolinska Universitetssjukhuset Solna

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-09-01
Primary Completion
2026-09-01
Completion
2027-09-01

Countries

  • Sweden

Study Locations

More Related Trials

Entities

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 NCT05906030 on ClinicalTrials.gov