CClinicalTrials.gg
CompletedNCT04656548Updated May 26, 2021

A Comparative, Retrospective Chart Review of Intended Dwell Time of a PICC Line

An observational study in Peripheral ICC and PICC, sponsored by Access Vascular Inc. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2021-05-26.

Sponsored by Access Vascular Inc · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
121
Sex
All
01

Study summary

This is a retrospective, matched pair comparative post market review of 4Fr Single Lumen PICC lines. The subjects will be matched by the timeframe of when the HydroPICCs were inserted.

Read the detailed description

Subjects would have received a 4 Fr Single Lumen PICC line between Aug 2020 and Oct 2020.

The two groups will be HydroPICCs and the standard of care for the facility.

A comparison of multiple endpoints will be evaluated between the two groups.

02

Conditions studied

  • Peripheral ICC
  • PICC
03

In context

Lead sponsor

Access Vascular Inc is the lead sponsor of 3 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Any patients at the study site that received a 4 Fr single lumen PICC line from Aug 2020 through Oct 2020.

Inclusion criteria

  • Subjects who have been inserted with the HydroPICC during a specific time range.
  • During the same time period, any competitor 4 Fr single lumen placed.

Exclusion criteria

Exclusion Criteria:

  • None
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
121 participants (actual)
Patient registry
No

Groups and cohorts

  • HydroPICC

    Cohort who received the HydroPICC

    Device: HydroPICC

  • Standard of Care

    Cohort who received something different than HydroPICC

Interventions

  • DeviceHydroPICC

    PICC lines

    Also known as: Standard of Care

06

What researchers measure

Primary outcomes

  1. Intended dwell time based on a comparison of the actual dwell time to the intended time

    Comparison of actual vs intended dwell times of each arm

    Time frame: August 2020 through October 2020

Secondary outcomes

  1. Comparison of failure rates

    Compare the failure rates between the two arms

    Time frame: August 2020 through October 2020

07

Study locations

1 site
  • Joseph Bunch
    Romeoville, Illinois 60446, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 26, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04656548
Lead sponsor
Access Vascular Inc
Responsible party
Sponsor
First posted
Dec 7, 2020
Start date
Nov 13, 2020
Primary completion
Apr 23, 2021
Completion
Apr 23, 2021
Last update
May 26, 2021

Study contacts

Joseph Bunch
principal investigator · ProVasc

Oversight

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

Not currently enrolling

This study is completed, as verified in May 2021. You cannot join it, but the record below documents what was studied.

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