Actively Recruiting

Age: 18Years - 100Years
All Genders
Healthy Volunteers
NCT05906030

Diaphragm Dysfunction and Ultrasound Perioperatively

Led by Karolinska University Hospital · Updated on 2025-01-29

160

Participants Needed

2

Research Sites

156 weeks

Total Duration

On this page

Sponsors

K

Karolinska University Hospital

Lead Sponsor

K

Karolinska Institutet

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Diaphragm Dysfunction and Ultrasound Perioperatively

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (18 years and older) scheduled for elective or acute abdominal, pelvic, or vascular surgery
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Having underlying chronic lung or respiratory disease
  • Unable to provide informed consent

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Karolinska University Hospital, Perioperative Medicine and Intensive Care

Stockholm, Stockholm County, Sweden, 17176

Actively Recruiting

2

Karolinska University Hospital

Stockholm, Sweden, 17176

Actively Recruiting

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Research Team

J

Jessica Kåhlin, MD, PhD

CONTACT

E

Emma Larsson, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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