Augmented Renal Clearance in the Adult Non-critically Ill Surgery Patient: a Prospective Point Pr… (NCT02228551) | Clinical Trial Compass
CompletedNot Applicable
Augmented Renal Clearance in the Adult Non-critically Ill Surgery Patient: a Prospective Point Prevalance Study
Belgium279 participantsStarted 2013-11
Plain-language 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 abdominal and trauma surgery population. Secondary objectives are the identification of risk factors associated with ARC in this specific study population.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* 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 Criteria:
* 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.