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Effect of urethral catheterization under sedation and analgesia before induction of anesthesia on postoperative catheter related bladder discomfort (CRBD)

Effect of urethral catheterization under sedation and analgesia before induction of anesthesia on postoperative catheter related bladder discomfort (CRBD)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048243
Enrollment
Unknown
Registered
2021-07-05
Start date
2021-07-02
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

anesthesia related complication

Interventions

Experimental group:urethral catheterization before induction of anesthesia
Control group:urethral catheterization after induction of anesthesia

Sponsors

The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18-75 years, male patients; 2. American Society of Anesthesiologists (ASA) grades I-III; 3. Patients undergoing non-urinary surgery under elective general anesthesia; 4. BMI is between 18-30kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Those with previous bladder outflow tract obstruction; 2. Patients with severe cardiovascular and cerebrovascular diseases, liver and kidney insufficiency and mental diseases; 3. Multiple catheterization failures; 4. Overactive bladder (nocturia > 3 times or urination frequency > 8 times in 24 hours); 5. Cognitive impairment or communication impairment; 6. Other circumstances in which the researcher judges that the subject is not suitable to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
The incidence of CRBD;

Secondary

MeasureTime frame
The severity of CRBD;

Countries

China

Contacts

Public ContactXu Qiqi

The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University

1455220822@qq.com+86 18752306055

Outcome results

None listed

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