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A prospective study on catheter-related bladder discomfort related to the volume of indwelling catheter balloons

A prospective study on catheter-related bladder discomfort related to the volume of indwelling catheter balloons

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091781
Enrollment
Unknown
Registered
2024-11-04
Start date
2024-11-05
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Urinary catheter related bladder irritation

Interventions

Experimental group (balloon volume 5ml):Inject 5ml of water into the catheter balloon
Control group (balloon volume 10ml):Inject 10ml of water into the catheter balloon

Sponsors

Shihezi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ASA I-III male patients, aged over 18 years, who plan to undergo general routine surgical procedures under general anesthesia (excluding urological surgery) and require indwelling catheterization for at least 6 hours.

Exclusion criteria

Exclusion criteria: Exclusion criteria: bladder outflow obstruction, overactive bladder, neurogenic bladder, history of urethral surgery.

Design outcomes

Primary

MeasureTime frame
The incidence of catheter-related bladder irritation (CRBD) 1 hour after tracheal extubation (the ratio of moderate to severe CRBD occurrence).;

Secondary

MeasureTime frame
The incidence and severity of CRBD (the rate of severe CRBD occurrence);Pain score;Time of catheter removal and adverse reactions;

Countries

China

Contacts

Public Contactche yingjie

Shihezi People's Hospital

751564366@qq.com+86 182 9907 2057

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026