Evaluation of ReDS Pro System V2.7 and ReDS ICU in Patients With Heart Failure
- Conditions
- Heart Failure
- Interventions
- Device: Remote Dielectric Sensing (ReDS)
- Registration Number
- NCT05405504
- Lead Sponsor
- Christian Hassager
- Brief Summary
The study is an investigator-initiated, prospective cohort trial. The trial aims to evaluate ReDS Pro System V2.7 and ReDS ICU in patients with heart failure (HF).
- Detailed Description
The study is an investigator-initiated, prospective cohort trial. The trial aims to evaluate ReDS Pro System V2.7 and ReDS ICU in patients with heart failure (HF). The overall purposes are:
* to evaluate the ReDS efficacy measurements of lung fluid compared to pulmonary artery pressure guided therapy with CardioMEMS in out-patients with HF.
* to describe the feasibility of ReDS ICU in patients admitted to an ICU with HF
For the out-patient part, the patients will be recruited from the outpatient clinic at Rigshospitalet. The patient must be at least 18 years, have a history of chronic HF, and already monitored using CardioMEMS and must not fulfill any of the exclusion criteria.
For the ICU part, the patients will be recruited at the ICU department at the Heart Center at Rigshospitalet. The patient must be at least 18 years, intubated, and unconscious or sedated (Glasgow Coma Score \<8), and already monitored using Swan-Ganz and arterial catherization and must not fulfill any of the exclusion criteria.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 25
ICU part:
- at least 18 years of age
- hospitalized in ICU setting at Rigshospitalet
- intubated
- unconscious or sedated (Glasgow Coma Score <8)
- monitored using Swan-Ganz and arterial catherization.
Out-patient part:
- at least 18 years of age
- history of Chronic heart failure > 3 months
- CardioMEMS
ICU part:
- pacemaker or ICD on the right side
- congenital heart malformations or intra-thoracic mass that would affect the right lung anatomy (e.g. dextrocardia, lung carcinoma)
- wounds, burns, healing tissue, skin infection or recent skin graft or flap where the sensors should be attached to the skin
- habitus is out of range due to one or more of the following
- height less than 155 cm or higher than 195 cm
- estimated BMI of less than 22 or more than 36
- standard active therapy has been stopped as the patient is inevitably dying.
Out-patient part:
- pacemaker or ICD on the right side
- congenital heart malformations or intra-thoracic mass that would affect the right lung anatomy (e.g. dextrocardia, lung carcinoma)
- wounds, burns, healing tissue, skin infection or recent skin graft or flap where the sensors should be attached to the skin
- habitus is out of range due to one or more of the following Height less than 155 cm or higher than 195 cm BMI of less than 22 or more than 38 For BMI 36 to 38, chest size ruler should be 39 or less
- cancer or other severe non-cardiac disease with estimated life expectancy less than 1 year
- planned hospitalization for ICD, pacemaker, lung or heart surgery including heart transplantation during the study period.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Out-patient part Remote Dielectric Sensing (ReDS) Chronic heart failure patients with CardioMEMS. ICU part Remote Dielectric Sensing (ReDS) Acute heart failure patients with Swan-Ganz catheter and an arterial catheter.
- Primary Outcome Measures
Name Time Method Correlation between ReDS ICU fluid parameters and Swan-Ganz measurements Daily Swan-Ganz catheter and ReDS ICU measurements the first 72 hours after Swan-Ganz implantation Measurements on Swan-Ganz catheter (CVP, PAP, PCWP - all in mmHg) and the percentage of fluid in the lungs (%)
Correlation between ReDS v2.7 fluid parameters and CardioMEMS measurements 3 months mPAP (mmHg), dPAP (mmHg) and the percentage of fluid in the lungs (%)
- Secondary Outcome Measures
Name Time Method Changes in ReDS ICU fluid parameters following changes in Positive End Expiratory Pressure During the first 72 hours after Swan-Ganz implantation The percentage of fluid in the lungs (%) and PEEP
Changes in ReDS ICU fluid parameters following changes administration of diuretics and inotropic/inodilators During the first 72 hours after Swan-Ganz implantation The percentage of fluid in the lungs (%)
Changes in ReDS ICU fluid parameters following changes in body position During the first 72 hours after Swan-Ganz implantation The percentage of fluid in the lungs (%)
Correlation between ReDS v2.7 fluid parameters and body weight 3 months The percentage of fluid in the lungs (%)
Changes in ReDS ICU fluid parameters following raised leg test During the first 72 hours after Swan-Ganz implantation The percentage of fluid in the lungs (%)
Correlation between ReDS v2.7 fluid parameters and dyspnea symptom evaluated by NYHA class. 3 months The percentage of fluid in the lungs (%)
Trial Locations
- Locations (1)
Rigshospitalet
🇩🇰Copenhagen, Denmark