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A prospective randomized comparative study between intelligent urinary bladder monitoring device and conventional urinary catheter in patients with voiding dysfunction caused by spinal cord injury

A prospective randomized comparative study on effects in preventing urinary tract infection between Intelligent urinary bladder monitoring device and conventional urinary catheter in patients with voiding dysfunction caused by spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005686
Enrollment
Unknown
Registered
2014-12-05
Start date
2015-01-01
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

Spinal cord injury

Interventions

Group with Intelligent urinary bladder monitoring :Using Intelligent urinary bladder monitoring device to manage urinate of patients
Group with urinary catheter :Using Conventional urinary catheter to manage urinate of patients

Sponsors

Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with voiding dysfunction caused by spinal cord injury within 24 hours; catheter retention required; 2. Vital signs were stable and no urethral complications; 3. Patients were no cognitive dysfunction and can complete the clinical trials with good compliance.

Exclusion criteria

Exclusion criteria: Patients wth spinal cord injury over 24 hours; patients diagnosed with urinary tract infections; Patients with history of specific or non-specific urinary tract infection.

Design outcomes

Primary

MeasureTime frame
midstream urine culture;—

Countries

China

Contacts

Public ContactXiaojian Cao
xiaojiancao001@163.com+86 13002505801

Outcome results

None listed

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