Prediction of urinary catheter-related bladder discomfort (CRBD) in patients with general anesthesia during the awakening period in the post-anesthesia care unit

Development a prediction model for catheter-related bladder discomfort in the post-anesthesia care unit

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000040128

Enrollment

Unknown

Registered

2020-11-22

Start date

2020-11-23

Completion date

Unknown

Last updated

2021-01-11

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

Conditions

Urinary catheter related bladder discomfort

Interventions

Indwelling urinary catheterization:Indwelling urinary catheterization

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Elective non-urological, non-cardiac, and non-ambulatory surgery; 3. Undergoing general anesthesia; 4. Requiring indwelling urinary catheterization; 5. Be willing to participate in research and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Unable to communicate after awakening in PACU; 2. Comorbid with cognitive dysfunction, or delirium after awakening in PACU; 3. A history of neurogenic bladder, preoperative urinary tract infection, and existed urinary frequency, urgency, and suprapubic discomfort; 4. ASA class>=IV, or comorbid with severe liver and renal dysfunction; 5. ICU admission or unplan ICU admission; 6. Allergic to general anesthesia drugs, unable to complete general anesthesia; 7. Participating in other clinical research.

Design outcomes

Primary

Measure	Time frame
The occurence and severity of CRBD;	—

Secondary

Measure	Time frame
VAS scores;	—

Countries

China

Contacts

Public ContactWangyuan Zou

Xiangya Hospital, Central South University

wangyuanzou@csu.edu.cn+86 13875814731

Outcome results

None listed

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