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Clinical study on the alleviation of urethral pain after removal of urinary catheter in men by pulsed intraurethral infusion of lidocaine hydrochloride + dexamethasone

Clinical study on the alleviation of urethral pain after removal of urinary catheter in men by pulsed intraurethral infusion of lidocaine hydrochloride + dexamethasone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102136
Enrollment
Unknown
Registered
2025-05-09
Start date
2024-01-04
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Relieve urethral pain before and after the removal of urinary catheter in male patients with long-term indwelling urinary catheter for more than 5 days or indwelling urinary catheter after transurethral surgery

Interventions

Experimental group:Pulse-type intraurethral infusion
control group:Routine intraurethral infusion

Sponsors

Fuling People's Hospital Of Chongqing
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Male patients aged 18 years or older requiring indwelling urinary catheterization for more than 5 days, or those who have undergone transurethral surgical procedures and require postoperative indwelling catheterization.

Exclusion criteria

Exclusion criteria: 1. Patients with drug allergies (particularly those allergic to medications used in this study); 2.Patients presenting with clinically significant bleeding following catheter removal; 3. Patients who refused or were non-compliant with medication instillation protocols; 4. Patients receiving concurrent drug therapies or currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
alleviate pain;

Secondary

MeasureTime frame
Satisfaction level;

Countries

China

Contacts

Public ContactZhao Sanshan

Fuling People's Hospital Of Chongqing

1057009278@qq.com+86 23 72860069

Outcome results

None listed

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