Lidocaine Analgesia for Urethral Catheterization in Children

Completed · Not applicable

Conditions studied: Pediatric Presentation of Urinary Tract Infection

In brief

Primary Aim 1\. To measure difference in pain via Faces, Legs, Activity, Cry and Consolability (FLACC) Pain Scale score at the time of transurethral bladder catheterization for urine collection in children who do and do not receive intraurethral 2% lidocaine jelly prior to catheterization. Secondary Aims 1. To assess gender differences in pain control during transurethral bladder catheterization with and without pain control using intraurethral 2% lidocaine jelly. 2. To assess patient discomfort with administration of intraurethral 2% lidocaine jelly. To assess parental impression of discomfort between intervention and control groups. 3. To assess pain associated with the administration of intraurethral 2% lidocaine jelly. 4. To measure difference in pain via Modified Behavioral Pain Scale (MBPS) score at the time of TUBC for urine collection in children who do and do not receive intraurethral 2% lidocaine jelly prior to catheterization.

Key facts

Study ID

NCT01780324

Run by

Seattle Children's Hospital

People needed

80

Starts

2013-01-01

Expected to finish

2015-05-01

Last updated by the study team

2016-04-11

Who can join

Age: any, up to 3. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 0-3 years
• English or Spanish speaking
• Legal guardian present to provide consent
• Medical indication for TUBC during the patient's ED visit

You may not qualify if…

• Severe developmental delay or impaired mentation
• Neural tube defect, paraplegia, or other condition altering urethral sensation
• Known urethral stricture, anatomic abnormality or reconstruction
• History of sexual abuse
• Patient weight less than 2.3 kg
• Allergy or previous adverse reaction to lidocaine
• Previous enrollment in the study
• Prior successful or attempted TUBC in previous 7 days

Where it is running

• Seattle Children's Hospital — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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