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Effects of different timings of urinary catheterization on catheter-related bladder discomfort in male patients after general anesthesia: a randomized controlled clinical trial

Effects of different timings of urinary catheterization on catheter-related bladder discomfort in male patients after general anesthesia: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064746
Enrollment
Unknown
Registered
2022-10-15
Start date
2022-10-15
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

catheter-related bladder discomfort

Interventions

Group Awake:No sedatives and analgesics will be administered, and a urinary catheter will be inserted in a conscious state, followed by induction of general anesthesia.
Group Sedation:Midazolam 0.02 mg/kg and sufentanil 0.1 ug/kg will be administered intravenously, and a urinary catheter will be inserted 5 minutes later, followed by induction of general anesthesia.
Group Induction:A urinary catheter will be inserted after successful induction of general anesthesia.

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male patients aged 18-65 who are going to undergo elective surgery under general anesthesia in Qilu Hospital of Shandong University and require indwelling a urinary catheter; 2. The surgical site is one of the four sites : the spine, the limbs, the thoracic cavity, and the abdominal cavity; 3. The patient agrees Participate in the trial and sign informed consent.

Exclusion criteria

Exclusion criteria: Those who meet any of the following criteria are excluded: 1. Complicated with prostate disease, urethral stricture, urethral injury or other urinary system diseases requiring treatment before surgery, with a history of urinary system surgery or the current urinary system surgery; 2. Preoperative self-reported symptoms such as frequent urination, urgency, and dysuria; 3. Preoperative cauda equina syndrome; 4. Plan postoperative delayed recovery or delayed removal of tracheal tube; 5. Communication barriers; 6.BMI30kg/m2; 7. Severe heart, lung, liver and kidney insufficiency; 8. There is a history of catheterization in the past; 9. There is a history of chronic pain or drug abusers; 10. Other circumstances that are not suitable for inclusion in the group.

Design outcomes

Primary

MeasureTime frame
Incidence of CRBD within 24 hours;

Secondary

MeasureTime frame
Severity of CRBD;Postoperative catheter-related adverse events;The success rate of one-time urinary catheter placement;urethral mucosal injury;Total additional amount of penehyclidine hydrochloride administered due to CRBD;Satisfaction with indwelling urinary catheters;Acceptance of the urinary-catheterization timing;

Countries

China

Contacts

Public ContactHongli Chen

Qilu Hospital of Shandong University

chl0910@126.com+86 18560083799

Outcome results

None listed

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