CClinicalTrials.gg
CompletedNCT03562013Updated Oct 11, 2019

Family Experience of Home Opioid Use After Pediatric Surgery

An observational study in Pain Management, sponsored by The Hospital for Sick Children. Completed at 1 site in Canada. Open to participants aged 1 Day to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-10-11.

Sponsored by The Hospital for Sick Children · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
89
Ages
1 Day to 18 Years
Sex
All
01

Study summary

A systematic review examining outpatient opioid use identified only three pediatric studies published between 2015 and 2016. Of these three, two studies had a short-term follow up with patients at three days after discharge; moreover, these three studies were limited by focusing on one surgical population, restriction of data to 0-12 yr old participants, and the other being a brief report. As a result, there are no pediatric studies that have examined opioid use amongst 0-18 yr olds, across multiple surgery types, and beyond 3 days after discharge.

Read the detailed description

This study is being done to learn how long children (0-18 yrs) needed to use the prescribed opioid medication for and how families can be better prepared to provide adequate and safe pain management at home. Follow up will take place 28 days after discharge from the hospital.

02

Conditions studied

  • Pain Management
03

In context

Lead sponsor

The Hospital for Sick Children is the lead sponsor of 568 studies on the registry; 81 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Any child (0-18 years) who has undergone a surgical procedure at The Hospital for Sick Children within 7 days of discharge.

Inclusion criteria

  • Families are filling a prescription for opioid medications at Shoppers Drug Mart at The Hospital for Sick Children
  • Parent has strong command of the English language (i.e., no interpreter required)

Exclusion criteria

Exclusion Criteria:

  • Child has used opioid medication at home within 6 months before the date of their surgical procedure
  • Child has history of chronic pain
  • Child is being discharged to a rehabilitation facility anticipated
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
89 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Questionnaire on Opioid use

    Questionnaire on how families provide adequate and safe pain management at home

    Time frame: 28 days following discharge from hospital

07

Study locations

1 site
  • The Hospital for Sick Children
    Toronto, Ontario M5G 1X8, Canada
08

References and documents

Publications

  • Feinberg AE, Chesney TR, Srikandarajah S, Acuna SA, McLeod RS; Best Practice in Surgery Group. Opioid Use After Discharge in Postoperative Patients: A Systematic Review. Ann Surg. 2018 Jun;267(6):1056-1062. doi: 10.1097/SLA.0000000000002591. PubMed 29215370 ↗
  • Caldeira-Kulbakas M, Stratton C, Roy R, Bordman W, Mc Donnell C. A prospective observational study of pediatric opioid prescribing at postoperative discharge: how much is actually used? Can J Anaesth. 2020 Jul;67(7):866-876. doi: 10.1007/s12630-020-01616-5. Epub 2020 Mar 12. PubMed 32166621 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 11, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03562013
Lead sponsor
The Hospital for Sick Children
Responsible party
Conor McDonnell (Staff Anesthesiologist, The Hospital for Sick Children) — Principal investigator
First posted
Jun 19, 2018
Start date
Jul 18, 2018
Primary completion
Mar 29, 2019
Completion
Jul 31, 2019
Last update
Oct 11, 2019

Study contacts

Conor Mc Donnell, MD
principal investigator · Staff Anesthesiologist

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion