Clinical Trials Detalhe
Impact of a Multimodal Intervention on Peripheral Venous Catheterization of Cancer Patients
Visão Geral
Gender
ALL
Idade
N/A
Fase
NA
Tipo de Estudo
INTERVENTIONAL
Localização
Instituto Português de Oncologia de Coimbra (Coimbra, Portugal)
Clinicaltrial.gov
https://classic.clinicaltrials.gov/ct2/show/NCT04085042Sumário
Peripheral intravenous catheterization (PIVC) is the most frequent invasive clinical procedure in a hospital setting, associated with significant complication rates for the patient, compromising their well-being, as well as the quality, safety, and efficacy of the care provided. The traditional approach to PIVC is considered reactive and ineffective, resulting in the exhaustion of the patients' peripheral venous access prior to consideration of other access methods and options (Moureau et al., 2012). Evidence suggests that the safety and effectiveness of patients with a peripheral catheter are also intrinsically associated with the adequacy of materials and technologies used in clinical contexts for vein selection, as well as for catheter insertion and maintenance care (Marsh, Webster, Mihala \& Rickard, 2017). Several studies point to the inadequacy of the technologies and medical devices used in this area, enhancing the occurrence of complications such as infection, phlebitis, occlusion and accidental catheter removal (Braga, 2017; Costa, 2017; Nobre \& Martins, 2018). The project investigators aim to determine whether the use of a PIVC pack will significantly reduce associated complications when compared with the usual care. Additionally, the research team aims to determine if the use of a PIVC pack will reduce the number of insertion attempts and overall procedure time, as well as improving patient and provider satisfaction.
Condições
Catheterization, Peripheral
Elegibilidade
Inclusion Criteria: * Participants who require peripheral intravenous catheterization as part of their therapeutic plan (caliber 20G or 22G); * Participants whose primary nurse agrees to participate in the study; * Participants who are able to give written assent or oral assent. Exclusion Criteria: * Confused and/or disoriented participants; * Participants who are unable to communicate orally and/or in writing.