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Intranasal Fentanyl Versus Placebo for Catheterization During a Voiding Cystourethrogram in Children

Intranasal Fentanyl Versus Placebo for Catheterization During a Voiding Cystourethrogram in Children

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00405444
Enrollment
64
Registered
2006-11-30
Start date
2006-11-30
Completion date
2008-09-30
Last updated
2010-12-13

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

Conditions

Pain

Keywords

Pediatrics, Pain, Voiding Cystourethrogram, Catheterization, Fentanyl

Brief summary

The purpose of this study is to determine whether intranasal fentanyl is better than placebo at decreasing pain in children 4-8 years of age during urinary catheterization for a VCUG study.

Detailed description

Studies have shown that the voiding cystourethrogram (VCUG) can be distressful and painful for children as the child is catheterized during the procedure. Currently no sedation or analgesia is recommended for the procedure. The practice of pediatrics is constantly seeking measures to decrease pain and distress for children. The opioid fentanyl was originally synthesized in the 1950's and 60's as an alternative to morphine and meperidine. The safety and efficacy of intranasal (IN) fentanyl has been previously demonstrated in the setting of a pediatric emergency department. We are proposing the use of IN fentanyl for analgesia prior to the catheterization for a voiding cystourethrogram (VCUG). If we prove that IN fentanyl is effective in reducing the pain while ensuring patient safety, it could become the analgesic of choice for this procedure.

Interventions

DRUGFentanyl

The dose of fentanyl that each child will receive will be 2 mcg/kg based on the child's weight. The medication will be administered 10 minutes prior to the procedure and will be dropped into the unoccluded nares over 1-2 seconds.

DRUGSterile water

The dose of sterile water that each child will receive will be 2 mcg/kg based on the child's weight. It will be administered 10 minutes prior to the procedure and will be dropped into the unoccluded nares over 1-2 seconds.

Sponsors

The Hospital for Sick Children
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
4 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

1. Age 4-8 years 2. Scheduled VCUG at Sick Kids 3. Understand the consent and assent form in English

Exclusion criteria

1. Previous adverse events to fentanyl or any opioid 2. History of a chronic respiratory or cardiac illness 3. Children with developmental delay 4. Children with bilateral nasal congestion.

Design outcomes

Primary

MeasureTime frame
Change in pain before and after catheterization for the VCUG.Will be measured up until 30 mins after the VCUG procedure.

Secondary

MeasureTime frame
Heart rate, respiratory rate and oxygen saturation just prior to and after the administration of fentanyl.Every 5 minutes until 30 minutes after the VCUG procedure.
Nausea, vomiting, itching, nasal pain/irritation or any other side effects.Will be measured up until 30 mins after the VCUG procedure.
Length of stay in diagnostic suiteTime frame determined by outcome

Countries

Canada

Outcome results

None listed

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