PROCOPrt-PAProlonged Hemodialysis Catheter Survival With Copolymer Coating and Rt-PA - PROCOPrt-PA Trial
rt-PA (2mg/2mL) actilysis
+ rt-PA
+ rt-PA (2mg/2mL) actilysis
Enfermedades Cardiovasculares
+ Enfermedades Vasculares
+ Trombosis
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de enero de 2011
Fecha en la que se inscribió al primer participante.The solution instilled into the central venous catheter lumens after each HD session and left in the catheter until the next session (catheter locking solution) is used to prevent thrombosis during the period between HD sessions and may also prevent catheter-related infection. However, evidence supporting the use of various locking solutions to achieve these objectives is limited. Heparin has been the traditional locking solution. Several small studies have assessed whether citrate and heparin are equally efficacious for maintaining catheter patency but the interpretation of the results was limited because the studies had a short follow-up period and included both uncuffed and cuffed central venous catheters. Thrombosis is a major cause of HD catheter dysfunction, and this problem is rectified by the use of thrombolytic agents, invasive procedures for declotting, or catheter replacement. A thrombus at the tip of the catheter or a fibrin sheath around it may resist local thrombolysis if it is not reached by sufficient concentrations of the drug. Urokinase has traditionally been used as the thrombolytic agent for HD vascular access declotting, and success rates for declotting vary from 55% to 85%. However, successful treatment of occluded central venous catheter (non HD) with recombinant tissue plasminogen activator (rt-PA) or alteplase was recently achieved in more than 1,000 patients with success (function restored in 798 patients [75.0%; 95% CI: 72.3 to 77.6%]). Serious adverse events monitored within 30 days was very rare and efficacy was independent of age, sex, body weight, and catheter type.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 240 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.De 18 a 79 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: End-stage kidney disease patients with newly inserted temporary untunnelled dual-lumen catheter Naive to study but not naive to catheters (both virgin and non-virgin catheters will be included) Expected to use catheter, and to dialyze at study centre, for at least six months Frequency of HD 3 times per week If indication for catheter was replacement for catheter related infection patients will be eligible after the infection has been treated and the patient has been off antibiotics for 3 HD sessions Patient or legal representative able to provide written consent Eighteen years of age or older Baseline INR ≤ 1.3 (no anticoagulation allowed outside the HD session) Baseline platelet count ≥ 60 x 109/L Exclusion Criteria: Use of systemic anticoagulation (if indication for anticoagulation is catheter patency patients may be eligible if the systemic anticoagulation is discontinued and baseline INR is ≤ 1.3) Insertion of a new catheter into the femoral vein Current use of antibiotics for catheter-related bacteraemia (see inclusion criteria above) Major haemorrhage in the prior 4 weeks, defined as bleeding resulting in a drop in haemoglobin of greater than 20 g/L or bleeding requiring transfusion of packed red blood cells with other clinical evidence or suspicion of bleeding History of intra-cranial bleed in the prior 4 weeks Intra-cranial or intra-spinal neoplasm (current) Allergy or intolerance to rt-PA or heparin or its constituents Active pericarditis - defined by the presence of a pericardial rub Weight ≤ 30 kg or > 130 kg Patient pregnant or lactating Child bearing potential (i.e. pre-menopausal woman who is not using a reliable method of contraception) Major surgery in past 48 hours (CABG, organ biopsy, puncture of non-compressible vessels), or scheduled for major surgery during the study period Involvement in another randomized drug trial Presence of a fever as defined by a temperature > 38.2°C
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.3 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalGrupo II
Comparador ActivoGrupo III
Comparador ActivoObjetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación
Centre Hospitalier du Centre du Valais (CHCVs)
Sion, SwitzerlandAbrir Centre Hospitalier du Centre du Valais (CHCVs) en Google Maps