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URIKA, continuous ultrasound monitoring of urinary bladder filling in patients with urinary retention

URIKA, continuous ultrasound monitoring of urinary bladder filling in patients with urinary retention - URIKA: Continuous monitoring of urinary bladder filling in adults

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43893
Enrollment
30
Registered
2015-09-02
Start date
2015-10-12
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary retention

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient is at least 18 years or older. Patient underwent surgery with spinal anaesthesia. Patient agree to participate in the study. Patient is capable of understanding the procedure.

Exclusion criteria

Exclusion criteria: Abdominal surgery (not possible to measure bladder via ultrasound). Known pregnancy. BMI > 25 Catheterized (urinary) patients

Design outcomes

Primary

MeasureTime frame
Best angle for fixating the ultrasound sensor, which give the most frequent bladder filling results during measurement.

Secondary

MeasureTime frame
The sensitivity and specificity will be calculated for the UBM, how well the threshold of 600 mL urine can be found in patients suffering POUR.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)