Study on the Nursing Effect of Non-Invasive Urinary Catheters for Women

Exploratory Study on the Nursing Effect of Non-Invasive Female Catheterization Sticks in Patients with Neurogenic Bladder Urinary Incontinence

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500112600

Enrollment

Unknown

Registered

2025-11-17

Start date

2025-11-17

Completion date

Unknown

Last updated

2025-11-24

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

Conditions

neurogenic bladder-related urinary incontinence

Interventions

Test group:Using non-invasive female urinary catheterization sticks

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Female, aged >= 18 years old; 2. Patients with spinal cord injury and urinary incontinence (disease duration>1 month) or cerebrovascular disease and urinary incontinence, who meet the diagnosis of neurogenic bladder; 3. Residual urine volume>100mL; 4. The subjects voluntarily participate in this study and sign an informed consent form (ICF) reviewed and approved by the ethics committee (EC) of the clinical trial institution; 5. The subjects are able and willing to comply with the operating procedures of the protocol,and cooperate with the collection of research data related to nurses, and agree to complete the follow-up according to the requirements of the plan.

Exclusion criteria

Exclusion criteria: 1. Severe urethral malformation; 2. Women who are breastfeeding, pregnant, or menstruating; 3. History of skin allergies; 4. Damage or rupture of the perineal skin , gynecological diseases, etc; 5. Acute urinary tract infection; 6. The researcher determines that it is not suitable for inclusion.

Design outcomes

Primary

Measure	Time frame
Urinary Tract Infection Rate ,Incontinence-Associated Dermatitis Rate;Comfort level, sleep quality, and mental state;	—

Secondary

Measure	Time frame
With reference to the intermittent catheterization training model for discharged patients, design a training course for family members or non-professional caregivers on the use of PureWick, so as to e;Explore the long-term application feasibility of non-invasive urinary catheterization protocols in home care.;Catheter-Related Bladder Discomfort (CRBD) Score: Comparison of Differences Between Invasive Catheterization and the Product;	—

Measure

Time frame

With reference to the intermittent catheterization training model for discharged patients, design a training course for family members or non-professional caregivers on the use of PureWick, so as to e;Explore the long-term application feasibility of non-invasive urinary catheterization protocols in home care.;Catheter-Related Bladder Discomfort (CRBD) Score: Comparison of Differences Between Invasive Catheterization and the Product;

—

Countries

China

Contacts

Public ContactWei Sun

Beijing Bo'ai Hospital

1742807141@qq.com+86 10 87569304

Outcome results

None listed

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