NL-OMON26134RecruitingNot Applicable
Validation of the BladderScans BVI 9400 and PRIME; Ultrasound Scanners for Measuring Bladder Volume Non-invasively
Medical Centre Leeuwarden0 sites300 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 300
Study Overview
Brief Summary
Brouwer TA, Eindhoven BG, Epema AH, Henning RH. Validation of an Ultrasound Scanner for Determing Urinary Volumes in Surgical Patients and Volunteers. J Clin Monit Comput; 1999, 15(6), 379-385.
Brouwer TA. Retenton d'Urine et Anomalies de la Miction en Postoperatoire. Le Practicien en Anesthesie reanimation. 2003; 7(2), 129-135.
Keita H, Diouf E, Tubach F, Brouwer T, Dahmani S, Mantz J, Desmonts JM. Predictive Factors of early Postoperative Urinary Retention in the Postanesthesia Care Unit. Anest.Analg. 2005; 101(2), 592-596.
Brouwer TA, Rosier PFWM, Moons KGM, Zuithoff NPA, Roon EN Kalkman CJ. Postoperative Bladder Catheterization Based on Individual Bladder Capacity: A Randomized Trial. Anesthesiology. 2015, 122(1), 46-54.
Study Design
- Study Type
- Observational
Eligibility Criteria
Inclusion Criteria
- •Adult patients (> 18 Y) who will be operated in the Medical Centre Leeuwarden needing a urinary catheter perioperatively and postoperative patients with a measured bladder volume larger than 500 ml and inability to void spontaneously provided written informed consent
Exclusion Criteria
- •Patients who have a suprapubic incision making the measurement impossible
Investigators
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