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Predictors and clinical intervention for postoperative catheter-related bladder discomfort

Predictors and clinical intervention for postoperative catheter-related bladder discomfort

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12004540
Enrollment
Unknown
Registered
2012-10-14
Start date
2014-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

postoperative catheter related bladder discomfort

Interventions

control group:saline
Experimental group 1:Tramadol
Experimental group 2:Butorphanol tartrate

Sponsors

Yijishan Hospital, Wannan Medical College, Wuhu 241001, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. All subjects undergone preoperative catheterize and catheter indwelling to postoperation; 2. Subjects are inpatients, and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. with urinary urgency and bladder symptoms before surgery; 2. with preoperative diagnosis of urinary tract infection; 3. with disorders of consciousness.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;Ramsay sedation score;—

Countries

China

Contacts

Public ContactLu Weihua

Wannan Medical College

lwh683@sohu.com+86 13955370637

Outcome results

None listed

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