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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02449317
Other study ID # 2558/171
Secondary ID
Status Completed
Phase N/A
First received May 17, 2015
Last updated August 31, 2017
Start date May 2015
Est. completion date January 2016

Study information

Verified date August 2017
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bioelectrical impedance analysis guided volume expansion for the prevention of contrast induced-acute kidney injury


Description:

Compared bioelectrical impedance analysis guided hydration therapy versus standard hydration for the prevention of contrast induced-acute kidney injury


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date January 2016
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

1. Age 18-90 yr

2. Chronic kidney disease stage 3 & 4 (eGFR 15-60 ml/min/m2)

3. elective cardiac catheterization

Exclusion Criteria:

1. Contrast media administration in the past 14 days

2. congestive heart failure (NYHA III-IV, ascites , pleuropericardial effusion ,severe valvular heart disease

3. Kidney transplant status or RRT

4. Emergency cardiac catheterization

5. Allergy to radiographic contrast media

6. Unstable renal function (change in serum creatinine = 0.5 mg/dl or 25% within 14 days prior to the study

7. Not inform consent

8. left ventricular ejection fraction < 40 %

9. Liver cirrhosis child B or C

10. Dosage of angiotensin-converting enzyme inhibitor /angiotensin II receptor blocker changed in past 2 wk

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Bioimpedance guided
bioelectrical impedance analysis guided hydration therapy : 7.5% Sodium bicarbonate 150 ml + 5% dextrose in water 850 ml IV in 6 hours rate was adjusted regarding to extracellular water/total body water extracellular water/total body water < 0.36 : 4 ml/kg/hr extracellular water/total body water 0.36-0.4 : 2 ml/kg/hr extracellular water/total body water > 0.4 : 1 ml/kg/hr
standard hydration
standard hydration : 7.5%Sodium bicarbonate 150 ml + 5% dextrose in water 850 ml IV 1 ml/kg/hr in 6 hours

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Outcome

Type Measure Description Time frame Safety issue
Primary serum creatinine at 48-72 hours after contrast administration Acute kidney injury 48-72 hr
Secondary serum creatinine at 2 weeks after contrast administration Renal replacement therapy 2 weeks
See also
  Status Clinical Trial Phase
Completed NCT03533348 - Preparative Fasting Before Contrast-enhanced Computed Tomography