Status:
COMPLETED
Augmented Renal Clearance in the Adult Non-critically Ill Surgery Patient: a Prospective Point Prevalance Study
Lead Sponsor:
Universitaire Ziekenhuizen KU Leuven
Conditions:
Prevalence of Augmented Renal Clearance
Risk Factors for Augmented Renal Clearance
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This point prevalence study investigates the prevalence of augmented renal clearance (i.e. a measured 8-hour urinary creatinine clearance \>= 120 ml/min/1.73m²) in an adult non-critically ill abdomina...
Detailed Description
This point prevalence study investigates the prevalence of augmented renal clearance (i.e. a measured 8-hour urinary creatinine clearance \>= 120 ml/min/1.73m²) in an adult non-critically ill abdomina...
Eligibility Criteria
Inclusion
- On the recruitment days, all non-critically ill adult patients hospitalized at the 74-bed abdominal and 50-bed trauma surgery wards in the 1850-bed University Hospitals Leuven were eligible for inclusion. On both wards, urinary collections are not routinely performed as part of standard of care.
Exclusion
- Exclusion criteria were age younger than 18 years
- Do not resuscitate (DNR) code ≥ 2
- Discharge before 16 hour on the day of collection (d0)
- Surgery on the day of collection Pregnancy, lactation
- Renal replacement therapy
- Non-Caucasian ethnicity
- Isolation in order for source control due to infection with multi-drug resistant organisms (MDRO)
- Incontinence or the lack of cooperation
- At the abdominal ward in particular
- Women without an indwelling urinary catheter were also excluded due to the incapacity of these patients to carry out the urinary collection in a safe and painless manner
- During the urinary collection, patients with incomplete or doubtful urinary collections were excluded
- Patients could only be included once, except for those with incomplete urinary collection at an earlier day of collection.
Key Trial Info
Start Date :
November 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2014
Estimated Enrollment :
279 Patients enrolled
Trial Details
Trial ID
NCT02228551
Start Date
November 1 2013
End Date
May 1 2014
Last Update
August 29 2014
Active Locations (1)
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1
Abdominal surgery ward and Trauma surgery ward, University Hospitals Leuven
Leuven, Vlaams Brabant, Belgium, 3000