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The effect of direct urinary catheter replacement among adults with UTI, systemic manifestations and indwelling catheter in comparison with replacement after two days of antibiotics.

The effect of direct urinary catheter replacement among adults with UTI, systemic manifestations and indwelling catheter in comparison with replacement after two days of antibiotics. - Urinary catheter replacement among adults with UTI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46399
Enrollment
30
Registered
2018-08-23
Start date
2018-08-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Cystitis Urinary tract infection UTI

Interventions

Group 1 (intervention group): After inclusion the catheter will be replaced immediately. Thereafter urine will be drawn from the new catheter for a second urine culture and antibiotics will be start

Sponsors

Deventer Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Presentation emergency department of the Deventer hospital - Indwelling catheter >=10 days and indication for replacement of the catheter - Fever >38,5C - No other infection found that can be accountable for the fever - Admission to a ward of DZ

Exclusion criteria

Exclusion criteria: - Antibiotics

Design outcomes

Primary

MeasureTime frame
The primary endpoint of this study is the number of days of hospitalization.

Secondary

MeasureTime frame
The secondary endpoints targets the clinical effect and the safety of the intervention. The endpoints measuring the clinical effectiveness are *days of fever* The endpoints measuring the safety of the intervention are patient reported side effects, registered complications, ICU admissions, death rate, and recurrence of UTI in 30 days after the intervention.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)