Duplex Ultrasonography Performed by Nurses

NCT ID: NCT03924583

Last Updated: 2019-04-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-03-18

Study Completion Date

2020-09-30

Brief Summary

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Catheter-related thrombosis (CRT) has been found as the major complication of the established central venous catheter in intensive care unit (ICU) patients. Its reported incidence varies from 5 to 66 %. Although most cases are asymptomatic, in up to 10 - 15 % of the patients pulmonary embolism occurs. In addition, CRT is associated with the risk of infection, post-thrombotic syndrome and with general disruption of the management of the underlying disease. The most accessible diagnostic method for CRT recognition is duplex ultrasonography. However, screening of CRT by duplex ultrasonography is not common approach in ICUs. Normally, duplex ultrasonography is performed by physicians. In this setting, implementation of the screening in ICU would be time consuming and practically unrealizable. Delegating this competence to ICU nurses can increase availability of this screening method.

Therefore, as a first step, investigators decided to perform a validation clinical study to verify the diagnostic accuracy of duplex ultrasonography of the venous system for CRT screening performed by a general nurse.

Detailed Description

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Approximately 150 patients with central venous catheter will be enrolled in this study.

Investigators:

1. General nurses - trained and able to perform duplex ultrasonography examination of venous circulation
2. Doctors - experienced specialists in intensive care or urgent medicine

Every patient with central venous catheter enrolled in clinical study is examined with duplex ultrasonography within 24 hours by both investigators, doctor and nurse. Each examination includes ultrasonography of a whole vena cava venous system with central venous catheter, bilaterally. Results of both examinations are blinded until the end of study, with one exception. In case of positive result - catheter related thrombosis is present, investigator ( nurse )informs patients attending physician.

Results of investigations are recorded in Investigation Form with some other routine medical data.

Timetable:

18.3.2019 - 30.6.2020: Enrolling, collection of data 1.7.2020 - 30.9.2020: Finalization od database, statistic analysis 1.10.2020 - 31.1.2021: Preparation of publications 1.2. 2021 - 31.12.2021: Result presentation

Conditions

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Catheter Related Complication

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Interventions

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Duplex ultrasonography

Ultrasound examination of whole vena cava venous system with central venous catheter inserted, using duplex US method to detect catheter related thrombosis

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* central venous catheter more than 48 hours in situ
* consent of a patient

Exclusion Criteria

* technical difficulties of ultrasound machine
* unfavorable local findings - inflammation of skin, excoriation etc.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Masaryk Hospital Krajská zdravotní a.s.

OTHER

Sponsor Role lead

Responsible Party

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Barbora Pakostová, M.D.

Medical doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Barbora Pakostová, M.D.

Role: PRINCIPAL_INVESTIGATOR

Krajská zdravotní a.s., Masaryk Hospital

Locations

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Clinic of anaesthesiology, resuscitaion and perioperative care, Masaryk Hospital,

Ústí nad Labem, , Czechia

Site Status RECRUITING

Countries

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Czechia

Central Contacts

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Barbora Pakostová, M.D.

Role: CONTACT

+420477112202

Facility Contacts

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Barbora Pakostová, M.D.

Role: primary

+420477112202

Other Identifiers

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258/40

Identifier Type: -

Identifier Source: org_study_id

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