VolumE maNagement Under Body Composition Monitoring in Critically Ill patientS on CRRT
Study Details
Study Description
Brief Summary
Although monitoring fluid balance for continuous renal replacement therapy-treated patients is an important issue, most physicians usually use conventional methods such as the difference between the amount of intake and output (I & O), which is not objective way. Meanwhile, bioimpedance electrical vector analysis presents the patients' fluid status with more objective data. Thus, the investigators will investigate the clinical benefit for monitoring fluid balance when the investigators use InBody S10, one of representative bioimpedance electrical vector analysis, compared with conventional methods among the patients who need continuous renal replacement therapy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Although monitoring fluid balance for continuous renal replacement therapy-treated patients is an important issue, most physicians usually use conventional methods such as the difference between the amount of intake and output (I & O), which is not objective way.
Meanwhile, bioimpedance electrical vector analysis presents the patients' fluid status with more objective data.
Thus, the investigators will investigate the clinical benefit for monitoring fluid balance by using InBody S10 (0, 1, 2-day, and 7-day from CRRT initiation), one of representative bioimpedance electrical vector analysis, compared with conventional methods among the patients who need continuous renal replacement therapy.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: IO group Fluid overload will be removed in the patients who received continuous renal replacement therapy, but the amount of fluid removal are guided by the intake-output balance. |
Other: IO group
Fluid removal are guided by intake-output balance.
|
| Experimental: InBody group Fluid overload will be removed in the patients who received continuous renal replacement therapy, but the amount of fluid removal are guided by the bioimpedance analysis (InBody S10). |
Device: InBody group
As one of representative BIVA, it provides the patients' fluid status with more objective data such as TBW, ECW, ICW, etc.
|
Outcome Measures
Primary Outcome Measures
- The rate reaching euvolemia [7 days from CRRT initiation]
To compare how many rates the two groups reach the euvolemia at 7 days from CRRT initiation
Secondary Outcome Measures
- Clinical outcomes (28-, 60-, 90-day mortality) [28-, 60-, or 90-days]
To compare the mortality rates between the two groups
Eligibility Criteria
Criteria
Inclusion Criteria:
- Patients will be eligible for INCLUSION in the study if ALL the following criteria are met;
-
The treating clinician believes that the patient requires continuous renal replacement therapy for acute renal failure.
-
The treating clinicians anticipate treating the patient with continuous renal replacement therapy for at least 72 hours.
-
Informed consent has been obtained.
-
The patient fulfills ONE of the following clinical criteria for initiating continuous renal replacement therapy:
urine output < 100 ml/6 hr that has been unresponsive to fluid resuscitation measures
-
K+> 6.5 mmol/L
-
pH < 7.2
-
Urea > 25 mmol/L
-
Clinically significant organ edema in the setting of acute kidney injury
- Patients who are over 5% of fluid overload or their total body water/height2 ≥13 L/m2
Exclusion Criteria:
- Patients will be EXCLUDED from the study if, in the opinion or knowledge of the responsible clinician ANY of the following criteria are present:
-
Patient age is < 18 years
-
Death is imminent (<24 hours)
-
There is a strong likelihood that the study treatment will not be continued in accordance with the study protocol.
-
The patient has been treated with continuous renal replacement therapy or other dialysis previously during the same hospital admission.
-
The patient has been on maintenance dialysis prior to the current hospitalization.
-
Any other major illness that, in the investigator's judgement, will substantially increase the risk associated with the subject's participation in this study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Bundang Seoul National University Hospital | Seongnam-si | Gyeonggi-do | Korea, Republic of | 13620 |
Sponsors and Collaborators
- Seoul National University Hospital
- Seoul National University Bundang Hospital
- SMG-SNU Boramae Medical Center
- Ewha Womans University Mokdong Hospital
Investigators
- Principal Investigator: Sejoong Kim, MD,PhD, Department of Internal Medicine, Bundang Seoul National University Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- VENUS