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Clinical Trials/NCT04391205
NCT04391205
Completed
Not Applicable

Safety and Efficiency oh the Use of Midline Peripheral Venous Catheter (MIDES)

A.O.U. Città della Salute e della Scienza1 site in 1 country211 target enrollmentApril 26, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Upper Extremity Deep Vein Thrombosis, Secondary
Sponsor
A.O.U. Città della Salute e della Scienza
Enrollment
211
Locations
1
Primary Endpoint
Number of participants with Peripheral deep venous thrombosis (DVP) suspected with Compression ultrasound (CUS) and confirmed by echodoppler
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Although the use of peripheral venous catheters (CVP) with brachial insertion with echo-guide (Midline) has increased significantly over the last 5-10 years, there are no sensitive data concerning complications in the literature during their use, particularly as regards incidence of thrombotic complication.The prospective observational study will enroll all the patients admitted to Home Health Hospitalization service, Geriatric Department and Intermediate Care service, to whom a Midline-type CVP will be placed for infusional therapy and who will give their consent to participate.

Registry
clinicaltrials.gov
Start Date
April 26, 2017
End Date
February 28, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
A.O.U. Città della Salute e della Scienza
Responsible Party
Principal Investigator
Principal Investigator

Dott.ssa RENATA MARINELLO

Principal Investigator

A.O.U. Città della Salute e della Scienza

Eligibility Criteria

Inclusion Criteria

  • Subjects admitted to wards adhering to the study (Home Health Hospitalization service, Geriatric Department and Intermediate Care service)
  • Subjects submitted to Midline type venous catheter insertion

Exclusion Criteria

  • History of deep venous thrombosis or pulmonary embolism
  • Be hospitalized for less than a week

Outcomes

Primary Outcomes

Number of participants with Peripheral deep venous thrombosis (DVP) suspected with Compression ultrasound (CUS) and confirmed by echodoppler

Time Frame: Once a week from the implant day until CVP removal or patient discharge, whichever came first, assessed up to 40 days

Deep vein thrombosis is investigated with Compression ultrasound (CUS) technique, scheduled once a week from the implant day or performed at the time of occurrence of device malfunctions or at the onset of symptoms resulting from thrombotic complications; echodoppler tecnique is used to confirm diagnosis of thrombosis.

Study Sites (1)

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