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临床试验/NCT02862197
NCT02862197Unknown不适用

Invasive Monitoring of Pulmonary Artery Pressure (PAP) Among Dialysis Treated Patients

Joint Authority for Päijät-Häme Social and Health Care1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2016年11月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
8
试验地点
1
主要终点
Change of pulmonary artery pressure (PAP) during the dialysis treatment

研究概览

简要总结

The purpose of this study is examine whether invasive pulmonary artery pressure (PAP) monitoring could be beneficial for the patients in dialysis treatment. Ten implantable pressure sensors (CardioMEMS ®) will be implanted and the PAPs of the individual participants are recorded during and in between the routine dialysis treatment sessions. This is an exploratory pilot study, where major interest lies in the values and changes in PAP in relation to other hemodynamic parameters among patients in dialysis treatment. Implanted device is only monitoring the patient without any effect on the actual treatment.

详细描述

Dialysis treatment is hemodynamically problematic in up to one third of the patients. Particularly, estimation of the adequate fluid removal during the dialysis can be difficult. Removing too much fluid can lead to dehydration, hypotension and dizziness, and insufficient removals can lead to fluid accumulation and worsening of possible heart failure. Both under- and overestimation of the fluid removal have been connected to increased mortality. Balancing the fluid balance is especially challenging in patients with simultaneous heart failure.

Several measures are made and precautions taken during the dialysis to optimize the ultrafiltration individually for each patient. The key question in the estimation of the right amount of ultrafiltration is, how much and at what speed fluid can be safely removed from the patient without critically lowering the filling and preload of the heart.

The results of the CHAMPION trial show that therapy guided by PAP is superior to conventional way in estimating the optimal fluid balance among heart failure patients. Compared to the heart failure patients in the CHAMPION trial, the ESRD patients share some similarities. In both groups, estimating the fluid balance is crucial, but difficult. The changes in fluid balance among ESRD patients are much larger.

In the present study the investigators aim to evaluate the potential of invasive measured PAP in the context of dialysis treatment for patients with end-stage renal disease (ESRD).

After the implantation the basic medical history is taken, echocardiography is made, and their laboratory measurements are recorded. Participants are then monitored during their routine dialysis treatment twice a week over the period of 1 month. In addition twice a day measurement is recorded in home during the study.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Any non-cardiac or non-renal medical condition causing the life-expectancy to be less than one year.
  • The patient is not able to take part of the study or the study can be considered to be harmful for the patient in the opinion of the investigator or the treating nephrologist.
  • Age >75 years
  • Age <18 years
  • Probable noncompliance
  • Subjects with an active infection
  • Subjects who, in the investigator's opinion, are unable to tolerate a right heart catheterization
  • Subjects who have had a major cardiovascular event (e.g., myocardial infarction, open heart surgery, stroke, etc.) within 2 months of the baseline visit
  • Subjects with a device (Pacemaker/Implantable Cardioverter-Defibrillator/CRT) implanted < 30 days prior to enrollment
  • Subjects with congenital heart disease or mechanical right heart valve(s)
  • Subjects likely to undergo heart transplantation or ventricular assist device implantation within 6 months of the baseline visit
  • Subjects with known coagulation disorders or subjects who are unable to take two types of blood thinning medications or anticoagulation therapy for one month after the sensor is implanted.
  • Subject is enrolled in another study with an active treatment arm
  • Pregnancy
  • Diameter of Pulmonary Artery <7-10 mm
  • Subjects with history of recurrent (> 1) pulmonary embolism or deep vein thrombosis

结局指标

主要结局

Change of pulmonary artery pressure (PAP) during the dialysis treatment

时间窗: PAP is recorded every ten minutes during the standard dialysis treatment (4-6h). Measurement is repeated twice a week for one month

次要结局

  • Change of pulmonary artery pressure (PAP) in between the dialysis treatment(measurement is made twice a day over the period of one month)

研究者

发起方
Joint Authority for Päijät-Häme Social and Health Care
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marjo Soini

study coordinator

Joint Authority for Päijät-Häme Social and Health Care

研究点 (1)

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