NCT03056859

Compass Device CVC Trial

Central Venous Catheterization in Obese Patients With Compass Device

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 20 (actual)
• Sponsor: University of New Mexico · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This is a single-arm observational trial of a device (Compass Vascular Access, Centurion Medical Products, Williamston MI). The device is a compact, sterile, single-use extravascular blood pressure transducer. This pressure measurement aids in confirmation of appropriate venous access. The investigators plan to enroll 40 consenting patients with BMI ≥35 who require central venous catheterization for clinical reasons independent of the existence of this study. The primary outcome is operator satisfaction.

Detailed description

Forty (40) consenting patients meeting inclusion/exclusion criteria for this single-arm observational trial will be prepared as usual for central venous catheter (CVC) placement. The Compass pressure measurement device will be included in the CVC placement apparatus as per the manufacturer's directions. Data will be recorded on the placement procedure, operator satisfaction, routine patient demographics, and incidence of inadvertent arterial puncture.

Conditions

• Blood Pressure

Interventions

Type	Name	Description
DEVICE	Extravascular blood pressure transducer	Listed device is included in central venous catheter placement apparatus for consenting patients, according to manufacturer directions

Timeline

• Start date: 2017-02-17
• Primary completion: 2020-02-10
• Completion: 2020-02-10
• First posted: 2017-02-17
• Last updated: 2024-06-27
• Results posted: 2024-06-27

Locations

1 site across 1 country: United States