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Catheter use evaluation in peripheral vein

Effectiveness of peripheral venous catheter

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-46zqr8
Enrollment
Unknown
Registered
2015-08-28
Start date
2014-08-04
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pathological conditions, signs and symptoms. adult

Interventions

Device
The sample size calculation, coming from a pilot test, pointed the minimum requirement of 75 adult patients admitted to medical and / or surgical units for each group researched. A catheter was only e

Sponsors

Universidade Federal do Paraná - UFPR
Lead Sponsor
Hospital de Clínicas da Universidade Federal do Paraná
Collaborator

Eligibility

Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Age between 18 and 100 years; both sexes; admitted to clinics / and / or surgical units searched the hospital; obtain peripheral venous access in the upper limbs, in gauges 20 and / or 22 gauges; prior authorization or first degree relative to participate in the study prior to venipuncture, by signing the Informed Consent and Informed.

Exclusion criteria

Exclusion criteria: Present fragility of peripheral venous network that prevents the puncture peripheral catheter; allergic reaction known to the material of catheters.

Design outcomes

Primary

MeasureTime frame
The expected outcomes are the primary are local complications of peripheral venous catheterization, verified through direct observation of the devices, as well as reading the records in physical records. The incidence of complications is detected based on literature Phillips (2001) and Infusion Nurses Society (INS, 2011).

Secondary

MeasureTime frame
Measurement and comparison of the length of stay in days of catheters in each group researched, free of complications, by direct observation of the devices and reading the records. Analysis of risk factors associated with local complications resulting by statistical calculations with the aid of Bioestat program. Analysis of the findings outcomes will be held immediately after the completion of data collection to the period of one year.

Countries

Brazil

Contacts

Public ContactDerdried Johann

Universidade Federal do Paraná - UFPR

derdried.johann@ifpr.edu.br+55(41)33853336

Outcome results

None listed

Source: REBEC (via WHO ICTRP)