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Comparison of Traditional Landmark versus Ultrasound Guided Placement of Percutaneous Tracheostomies in Adult Intensive Care Patients -­ A Randomised Controlled Trial

Comparison, in adult intensive care patients, of ultrasound guided versus traditional landmark guided placement of percutaneous dilatational tracheostomies to determine effect on tracheostomy position.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000237987
Acronym
TARGET Study ­ (Traditional landmArk versus ultRasound Guided Evaluation Trial)
Enrollment
50
Registered
2011-03-04
Start date
2011-08-23
Completion date
2012-07-06
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The TARGET Study is a prospective, randomised controlled trial, evaluating two standard techniques of tracheal puncture during insertion of percutaneous tracheostomies: the traditional landmark method versus the ultrasound guided method. Percutaneous Dilatational Tracheostomy (PTD) is a frequently performed invasive procedure in the Intensive Care setting, where complications both immediate and short term can contribute to significant morbidity and mortality. It is increasingly recognised that lateral (off midline) and cranio­caudal (too high up or too low down) malposition of PDTs may result in greater incidence of both short and long term complications. The use of ultrasonography in placing tracheostomies is well described in the literature. We aim to evaluate the use of real­time ultrasound guidance for the tracheal puncture, which is the most important determining element in positioning the tracheostomy, to determine which method results in better midline and cranio­caudal placement. Better midline and cranio-caudal placement in turn may decrease complications and improve clinically significant surrogate markers of outcome.

Interventions

Real time ultrasound guidance will be used to determine tracheal midline and cranio-caudal distance (i.e number of tracheal rings) from the cricoid catilage to determine the the site of the tracheal puncture which is the initial step in a percutaneous dilatational tracheostomy. A bronchoscopic image will be taken after the puncture which will be used to evaluate the puncture position during data analysis. After the puncture, insertion of the tracheostomy will proceed as per the routine used for

Real time ultrasound guidance will be used to determine tracheal midline and cranio-caudal distance (i.e number of tracheal rings) from the cricoid catilage to determine the the site of the tracheal puncture which is the initial step in a percutaneous dilatational tracheostomy. A bronchoscopic image will be taken after the puncture which will be used to evaluate the puncture position during data analysis. After the puncture, insertion of the tracheostomy will proceed as per the routine used for insertion of a percutanous dilatational tracheostomy. The entire procedure is expected to last between 15-30 minutes.

Sponsors

Royal Prince Alfred Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All adult intensive care patients where a decision has been made to insert a percutaneous dilatational tracheostomy

Exclusion criteria

Under 18 years old Pregnant women

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 19, 2026