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Efficacy of Lidocaine Gel in Reducing Foley Catheter Discomfort in Surgical Patients

Exploring the Potential Efficacy of Lidocaine Gel in Reducing Discomfort in Patients Undergoing Surgical Procedures Requiring Foley Catheter Placement

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02709304
Enrollment
40
Registered
2016-03-16
Start date
2016-04-30
Completion date
2017-01-31
Last updated
2016-03-16

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

Conditions

Urinary Catheter Discomfort in Surgical Patients

Keywords

urinary catheter discomfort

Brief summary

This study will evaluate whether lidocaine gel for urinary catheter insertion would decrease pain and discomfort associate with Foley catheters upon awakening from general anesthesia in the post anesthesia care unit. As a secondary objective, the study will evaluate bacterial colony counts from urine obtained from the surgical patients after insertion of the Foley catheter prior to prophylactic antimicrobial administration.

Interventions

Gel used for insertion of urinary catheter containing local anesthetic to determine if patients have less discomfort postoperatively when this is used

DRUGstandard gel

Standard gel that is used to insert a urinary catheter that does not contain local anesthetic

Sponsors

Creighton University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
19 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Males requiring catheterization for surgical procedures scheduled for less than 4 hours.

Exclusion criteria

* Females, patients with preexisting urological conditions, and infections

Design outcomes

Primary

MeasureTime frameDescription
Decrease postoperative urinary catheter related discomfortWithin 1 hour of emergence from general anestheticSubject and objective pain scale

Secondary

MeasureTime frameDescription
decreased incidence of bacteriuriaimmediate post catheter insertion and at 2 hour time pointUrine culture and colony counts

Contacts

Primary ContactMark D Reisbig, MD PhD
mdr44643@creighton.edu402-449-4847

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026