Indwelling catheterization
Conditions
Interventions
Intervention group:Supersmooth silicone catheter indwelling
Control group:Indwelling of ordinary silicon catheter
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Age above 18 years old, gender unlimited; (2) The patient voluntarily participated in the experiment and signed the informed consent; (3) no urethral infection or other urethral injury; (4) non-hepatitis A, hepatitis B, AIDS, tuberculosis and other infectious diseases in the active stage;
Exclusion criteria
Exclusion criteria: (1) Pregnant women or parturients; (2) Operation with infection or serious contamination; (3) Body temperature > 38 degree; (4) Refractory infections requiring treatment for more than 14 days; (5) Patients with self-intermittent catheterization; (6) those with suprapubic/percutaneous nephrostomy; (7) having mental disorders; (8) allergy to silicone; (9) Other immunosuppressive diseases or diseases that researchers do not consider appropriate for this clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain;Bacterial biofilm production; | — |
Secondary
| Measure | Time frame |
|---|---|
| Catheter associated bladder irritation;Catheter-associated urinary tract infection;Blockage of catheter;Catheter urine salt deposition;Satisfaction with indwelling catheter;complication; | — |
Countries
China
Contacts
Public ContactLingli Li
West China Hospital, Sichuan University
Outcome results
None listed