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The effects of intravesical alkalinized lidocaine in combination with atropine on catheter-related bladder discomfort

The effects of intravesical alkalinized lidocaine in combination with atropine on catheter-related bladder discomfort

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-15007438
Enrollment
Unknown
Registered
2015-11-05
Start date
2015-11-01
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

Catheter related bladder discomfort

Interventions

Group A:infusion of diluated atropine (27ml)
Group LA:2% lidocaine 20ml + Atropine 1mg/2ml + 0.9% NS 5ml
Group LAS:2% lidocaine 20ml + Atropine 1mg/2ml + 5% Sodium bicarbonate 5ml

Sponsors

The Fourth Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Male patients with an ASA physical status I and II; 2. selective operation patients suffering from non-urologic surgical procedures; 3. The patients have urinary tract catheterization after induction of general anesthesia; 4. It is the first time for the patient to indwell urinary catheter.

Exclusion criteria

Exclusion criteria: 1. Patients with history of OAB (urinary frequency 3 times at night and 8 times in 24 hours)and urethral stimulant symptoms; 2. Patients are difficult to communicate; 3. Patients with hypersensitivity to amide local anesthetics; 4. BWI?25 kg/m2 or BWI<19 kg/m2.

Design outcomes

Primary

MeasureTime frame
severity of catheter-related bladder;visual analogue scale (VAS);plasm concentration of lidocaine;plasm concentration of lidocaine;plasm concentration of lidocaine;plasm concentration of lidocaine;plasm concentration of lidocaine;

Secondary

MeasureTime frame
Ramsay scale;HR;BP;SpO2;

Countries

China

Contacts

Public ContactXuesong Ma
mxs13613630888@163.com+86 13613630888

Outcome results

None listed

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