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Clinical Trials/NL-OMON26134
NL-OMON26134
Recruiting
Not Applicable

Validation of the BladderScans BVI 9400 and PRIME; Ultrasound Scanners for Measuring Bladder Volume Non-invasively

Medical Centre Leeuwarden0 sites300 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Medical Centre Leeuwarden
Enrollment
300
Status
Recruiting
Last Updated
2 years ago

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Medical Centre Leeuwarden

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

Outcomes

Primary Outcomes

Not specified

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