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A Randomized Control Trial Comparing Single vs. Multiple Application of Lidocaine Analgesia Prior to Urethral Catheterization Procedures

Primary Purpose

Urinary Tract Infection, Kidney Diseases, Ureteral Diseases

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
observed levels of pain
Sponsored by
Children's Mercy Hospital Kansas City
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Tract Infection focused on measuring Topical analgesia, Urinary catheterization, FlACC Pain Scale, Lidocaine jelly

Eligibility Criteria

2 Months - 7 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Outpatient procedures only Voiding Cystourethrograms Nuclear Medicine Cystograms Nuclear Medicine Renal Mag 3 scans All of above require a urinary catheterization Exclusion Criteria: Legal guardian(s) is/are not present for permission Patients with altered levels of pain perceptions (i.e. patients with Spina Bifida, prior known sexual abuse, prior urethral surgery or prior urethral trauma) Patients with a current or past history of consistent catheterization Patients who are/have been sedated or anesthetized Patients who are requiring urine testing other than routine urinalysis and/or culture, as per our present policy of the exclusion of Lidocaine pre-analgesia for other urine studies. Any infant or child with a known sensitivity or allergy to Lidocaine or the "Caine" family of medicines. Hematology/Oncology patients with neutropenia.

Sites / Locations

  • Children's Mercy Hospital

Outcomes

Primary Outcome Measures

Cumulative pain score utilizing the FLACC pain scale(0-10), for pediatric patients age 2 months through 7 years of age.

Secondary Outcome Measures

Other data collected:
patient age in years/months
gender
race/ethnicity
patient heart rate pre-catheterization and at time of
catheterization
type of procedure requiring catheterization
time of procedure
type of age-appropriate child life techniques used during
the procedure
parental survey

Full Information

First Posted
August 31, 2005
Last Updated
April 16, 2007
Sponsor
Children's Mercy Hospital Kansas City
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1. Study Identification

Unique Protocol Identification Number
NCT00142064
Brief Title
A Randomized Control Trial Comparing Single vs. Multiple Application of Lidocaine Analgesia Prior to Urethral Catheterization Procedures
Official Title
A Randomized Control Trial Comparing Single to Multiple Application Lidocaine Analgesia Prior to Urethral Catheterization Procedures
Study Type
Interventional

2. Study Status

Record Verification Date
September 2006
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Children's Mercy Hospital Kansas City

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if a single application of Lidocaine gel topical anesthesia is as effective in decreasing the discomfort associated with urinary catheterization as two applications, within our pediatric population. Currently, two applications is our standard of care within our pediatric Radiology Department. Urinary catheterization is the process of placing a flexible tube into the urinary opening (urethra), to drain urine or instill radiographic solution for study of the anatomy and/or function of the urinary system. Members of the study team hypothesize equivalence in the observer reported catheterization pain scores as measured by the FLACC pain scale. The study is designed to obtain conclusive data to guide clinical practice. The study team hypothesizes that statistically similar levels of analgesia will be observed with the single application procedure as compared to the multiple application technique.
Detailed Description
This randomized control trial is designed to obtain conclusive data to guide clinical practice and will be a single site study. The study examines variations in observer reported catheterization pain levels when pre-treatment occurs through either a single application technique or a double application strategy. Two treatment groups have been established for this investigation with individual assignment into either of the two cohorts occurring through randomization. These two intervention groups include (1) usual care with two applications (the control group) and (2) single application (study group). Those patients randomized to the control group will receive one application of gel externally and one internal application of Lidocaine gel internally into the urethra, five minutes apart. The final application occurs five minutes prior to catheterization. The second group of patients is randomized to a pre-catheterization analgesia strategy that uses one internal application five minutes prior to catheterization. 400 patients from two months through 7 years of age will be invited to participate in the study. The primary outcome variable will be the cumulative FLACC pain score. The FLACC pain scale is a simple graph for scoring the distress behavior or observed pain responses in children who may not be able to rate the presence or severity of pain. One consistent observer will be utilized to provide the scoring of this pain scale, and will remained blinded to the method of Lidocaine application to which the child is randomized. A Child Life Specialist will be responsible for offering age-appropriate diversion and comfort techniques during the procedure. A parental survey will be completed by the parent(s) at the conclusion of the study, to be collected in a locked survey box.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Infection, Kidney Diseases, Ureteral Diseases, Ureteral Obstruction
Keywords
Topical analgesia, Urinary catheterization, FlACC Pain Scale, Lidocaine jelly

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
observed levels of pain
Primary Outcome Measure Information:
Title
Cumulative pain score utilizing the FLACC pain scale(0-10), for pediatric patients age 2 months through 7 years of age.
Secondary Outcome Measure Information:
Title
Other data collected:
Title
patient age in years/months
Title
gender
Title
race/ethnicity
Title
patient heart rate pre-catheterization and at time of
Title
catheterization
Title
type of procedure requiring catheterization
Title
time of procedure
Title
type of age-appropriate child life techniques used during
Title
the procedure
Title
parental survey

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Outpatient procedures only Voiding Cystourethrograms Nuclear Medicine Cystograms Nuclear Medicine Renal Mag 3 scans All of above require a urinary catheterization Exclusion Criteria: Legal guardian(s) is/are not present for permission Patients with altered levels of pain perceptions (i.e. patients with Spina Bifida, prior known sexual abuse, prior urethral surgery or prior urethral trauma) Patients with a current or past history of consistent catheterization Patients who are/have been sedated or anesthetized Patients who are requiring urine testing other than routine urinalysis and/or culture, as per our present policy of the exclusion of Lidocaine pre-analgesia for other urine studies. Any infant or child with a known sensitivity or allergy to Lidocaine or the "Caine" family of medicines. Hematology/Oncology patients with neutropenia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brenda K Boots, BSN
Organizational Affiliation
Children's Mercy Hospital Kansas City
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Mercy Hospital
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States

12. IPD Sharing Statement

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A Randomized Control Trial Comparing Single vs. Multiple Application of Lidocaine Analgesia Prior to Urethral Catheterization Procedures

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