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CompletedNCT03121794Updated Sep 18, 2020

Ultrasonographic Identification of the Proximal Humerus Landmarks

An observational study in Proximal Humerus Interosseous Venous Access, Anatomic Landmark and Ultrasonography, sponsored by The Cleveland Clinic. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-09-18.

Sponsored by The Cleveland Clinic · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

Evaluate whether discrete landmarks of the proximal humerus can be identified using ultrasound in patients with various body habitus and BMI.

Read the detailed description

There are three main forms of vascular access: peripheral intravenous (PIV), Central venous (CV) and intraosseous (IO). Of the different types of vascular access PIV and CV access have drawbacks when used during resuscitation, because they can be difficult to obtain when patients are volume depleted as in cases of trauma. Attempting CV access has numerous risks with complications occurring in up to 33% of attempts. These include failed placement (22%), arterial puncture (5%), catheter malposition (4%), pneumothorax (1%) and asystolic cardiac arrest (\<1%). Attempting to obtain CV access may also disrupt chest compressions in cases of cardiac arrest. Intraosseous access has been used in scenarios where PIV and CV access is difficult or impossible to obtain. Pharmacokinetic studies and standard practice support the bioequivalence of intraosseous and intravenous administration of common medications. Intravascular depletion does not hinder attempts at IO access, and as the insertion sites are peripheral to the heart, insertion can be done avoiding interruptions in chest compressions. Obtaining proximal humerus interosseous (PHIO) access may also be faster than obtaining both PIV and CV access with a relatively low complication rate. In one survey, complications of IO included difficulty in identifying correct anatomical site (3%), extravasation (3.7%), displacement after insertion (8.5%), and very rarely late complications including compartment syndrome (0.6%), osteomyelitis (0.4%) and skin infection (0.3%).

02

Conditions studied

  • Proximal Humerus Interosseous Venous Access
  • Anatomic Landmark
  • Ultrasonography

Keywords

  • ultrasonography
  • Intraosseous Vascular access
  • humerus
  • anatomic landmark
03

In context

Lead sponsor

The Cleveland Clinic is the lead sponsor of 818 studies on the registry; 118 are open to participants now.

Of its 89 completed or terminated interventional studies of FDA-regulated products, 72 (81%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants will be selected after chart review of current patients undergoing general, cardiac, thoracic, or vascular surgery. Patients will be approached in the preoperative clinic or during their hospitalization (preoperatively or postoperatively). Informed consent will be obtained prior to performing the study.

Participants will be separated into 3 cohorts based on BMI. The number of participants in each cohort is as follows: 10 patients with BMI 18.5 - 25 kg/m2; 10 patients with BMI 30-35 kg/m2, 10 patients with BMI > 40 kg/m2.

Inclusion criteria

  • Males or females 18 years of age or older undergoing general, cardiac, thoracic or vascular surgery.
  • BMI >= 18.5 kg/m\^2

Exclusion criteria

Exclusion Criteria:

  • Limited mobility/ range of motion of arms
  • Prior surgical intervention on shoulder or humerus
  • History of arm dislocation with internal rotation
  • History of arm fracture
  • BMI in ranges: 25.1 - 29.9, 35.1 - 39.9
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (actual)
Patient registry
No

Groups and cohorts

  • Low BMI

    Ultrasonographic identification of proximal humerus landmarks for patients with BMI 18.5 - 25 kg/m2

    Procedure: Ultrasonographic exam · Device: ultrasound machine

  • Moderate BMI

    Ultrasonographic identification of proximal humerus landmarks for patients with BMI 30-35 kg/m2 will receive ultrasound exam.

    Procedure: Ultrasonographic exam · Device: ultrasound machine

  • High BMI

    Ultrasonographic identification of proximal humerus landmarks for patients with BMI \> 40 kg/m2 will receive ultrasound exam.

    Procedure: Ultrasonographic exam · Device: ultrasound machine

Interventions

  • ProcedureUltrasonographic exam

    The study team will perform an ultrasonographic exam of the proximal humerus to identify six anatomical landmarks

  • Deviceultrasound machine

    Regular ultrasound machine used at Cleveland Clinic

06

What researchers measure

Primary outcomes

  1. Number of proximal humerus landmarks successfully identified by ultrasound exam

    Two investigators will perform an ultrasonographic exam on each patient, with one investigator examining each side of the body. Each investigator will aim to identify 6 anatomical landmarks: 1. The humeral shaft, 2. The surgical neck of the humerus, 3. The lesser tubercle, 4. The greater tubercle, 5. The intertubercular sulcus 6. The target site in the greater tubercle for needle insertion. Each side will receive a score ranging from 0 to 6 corresponding to the number of landmarks correctly identified.

    Time frame: Through completion of ultrasonographic exam, an average of 30 minutes.

Secondary outcomes

  1. Time used to identify all 6 anatomical landmarks using ultrasound in seconds.

    Evaluate the time used to identify all 6 anatomical landmarks using ultrasound.

    Time frame: Through completion of ultrasonographic exam, an average of 30 minutes.

  2. Depth of each landmark from the skin in centimeters.

    Depth of each landmark from the skin in centimeters based on ultrasound measurements.

    Time frame: Through completion of ultrasonographic exam, an average of 30 minutes.

07

Study locations

1 site
  • Cleveland Clinic
    Cleveland, Ohio 44195, United States
08

References and documents

Study documents

  • Protocol and statistical analysis plan · Dec 1, 2016

Documents are hosted by the registry — open the source record to download them.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03121794
Lead sponsor
The Cleveland Clinic
Responsible party
SergioB17 (Principal Investigator, The Cleveland Clinic) — Principal investigator
First posted
Apr 20, 2017
Start date
Apr 1, 2017
Primary completion
Oct 19, 2019
Completion
Jul 7, 2020
Last update
Sep 18, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

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