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Negative Venous Line Pressure in a Miniaturised Cardiopulmonary Bypass Circuit (CPB)

NCT03717649 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2018-10-24

No results posted yet for this study

Summary

Study to measure the ability of a 'fenestrated' venous line cannula to reduce the negative line pressure seen with kinetic-assist active venous drainage (KAVD) in a standard miniaturised cardiopulmonary bypass circuit and thereby increase the flow characteristics of the bypass pump.

Conditions

  • Heart Surgery

Interventions

DEVICE

Conventional 2-stage venous cannula

venous cannula

DEVICE

Conventional 3-stage venous cannula

venous cannula

DEVICE

Fenestrated 3-stage venous cannula

venous cannula

Sponsors & Collaborators

  • University Hospital Plymouth NHS Trust

    lead OTHER

Principal Investigators

  • Mark Bennett, MD · University Hospitals Plymouth NHS Trust

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-12
Primary Completion
2016-10-31
Completion
2016-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03717649 on ClinicalTrials.gov