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NCT05957653

Lidocaine Combined With Sufentanil for Preventing Catheter-related Bladder Discomfort

Status unknown Phase 4 Last updated 24 July 2023
What this trial tests

Phase 4 trial testing lidocaine and sufentanil in Prostate Cancer in 140 participants. Status unknown.

Timeline
7 October 2023
Primary endpoint
30 September 2025
30 October 2025

Quick facts

Lead sponsorRenJi Hospital
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment140
Start date7 October 2023
Primary completion30 September 2025
Estimated completion30 October 2025

Drugs / interventions tested

Conditions studied

Sponsor

RenJi Hospital

Who can join

Adults 18 to 79, male only, with Prostate Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical trial is to evaluate the incidence and severity of postoperative catheter-related bladder discomfort after robot-assisted radical prostatectomy. The main question it aims to answer is to evaluate incidence of CRBD immediately after extubation in resuscitation. A total of 20ml of 2% lidocaine and 1μg/ml sufentanil or 20ml normal saline was injected into the bladder of the participants through the catheter. After drug injection, the catheter was clamped for 20 minutes, and then 100ml normal saline was injected into the bladder through the catheter to flush out. Then, the incidence of CRBD was compared between the two groups.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Prostate Cancer

Currently open trials in the same condition.

Other RenJi Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05957653.

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