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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05702515
Other study ID # 2022-03
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date July 21, 2023
Est. completion date August 15, 2024

Study information

Verified date January 2024
Source Teleflex
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study is to collect intravascular and extravascular echocardiogram (ECG) data from subjects receiving peripherally inserted central catheters (PICC) while using the Vascular Positioning System G4 and a 12 lead ECG machine. The data obtained will be used to update the G4 algorithm.


Description:

This study seeks to collect synchronized digital data collected from the G4 and ECG machines during the PICC insertion procedure. A copy of the data will be downloaded from the G4 and ECG machines and submitted to the sponsor. Both the G4 and the ECG machine used for data collection in this study are FDA cleared/approved. Study Design: This is a single center prospective clinical study. All enrolled subjects will receive a 12-lead ECG during PICC insertion and a chest x-ray post insertion. ECG lead will be documented via photographic imaging. Duration of Subject Study Participation: Each subject's participation will start at the time of signing the informed consent and terminate upon completion of the x-ray.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 25
Est. completion date August 15, 2024
Est. primary completion date July 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 21 Years and older
Eligibility Inclusion Criteria: - Male - 21 years of age or older - Scheduled for PICC insertion using the VPS G4 system - Willing to allow thoracic photos to be obtained after ECG lead placement Exclusion Criteria: - Female - ? 21 years of age - Patient has a pacemaker - Patient condition precluding ECG use and lead placement - Patient condition precluding radiographic imaging - Unwilling to allow thoracic photos to be obtained after ECG lead placement

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Digital ECG Data Collection
synchronized digital data collected from the G4 and ECG machines during the PICC insertion procedure

Locations

Country Name City State
United States Duke University Hospital Durham North Carolina

Sponsors (2)

Lead Sponsor Collaborator
Teleflex Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary VPS G4 system digital data VPS G4 digital captured data recorded at 11.667 MHz measuring ISPTA.3 (mW/cm2) vs time (s). During PICC insertion procedure
Primary Electrocardiograph digitally captured data Electrocardiograph digitally captured data recorded at a sample resolution of 4.88 µV/LSB @ 250 sps, 1.22 µV/LSB @ 500 sps and a frequency response of -3 dB @ 0.01 to 150 Hz vs time (s). During PICC insertion procedure
See also
  Status Clinical Trial Phase
Completed NCT04656548 - A Comparative, Retrospective Chart Review of Intended Dwell Time of a PICC Line
Terminated NCT04920929 - PICC Asymptomatic Thrombosis Study: A Pilot Study N/A