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Opioid Use, Storage, and Disposal Among Pediatric Patients After Surgery

Primary Purpose

Tonsillitis, Sleep Disordered Breathing, Hernia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Disposal Aid
Sponsored by
Nationwide Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tonsillitis

Eligibility Criteria

1 Year - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Parent or legal guardian of a child having outpatient otolaryngologic or urologic surgery at Nationwide Children's Hospital
  • Child's age is between 1 and 17 years
  • Child is expected to receive a discharge opioid prescription

Exclusion Criteria:

•Unable or unwilling to track pain medication use or complete a follow-up survey

Sites / Locations

  • Jennifer Cooper

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Deterra Bag

Control

Arm Description

These families will receive a Deterra® bag (a drug Disposal Aid) and instructions on its use by a research team member.

These families will receive routine postoperative instructions only.

Outcomes

Primary Outcome Measures

Proper disposal of unused opioids
The proper disposal of unused opioids, defined as the disposal of unused opioids by an FDA-recommended method or by using the Deterra® drug deactivation system.

Secondary Outcome Measures

Quantity of opioid used after surgery
Number of doses of opioid pain medication used after surgery
Quantity of opioid leftover after surgery
Number of doses of opioid pain medication leftover after surgery
Proper storage of opioids
Whether the opioids were properly stored after surgery
Barriers to opioid disposal
What the parent/caregiver perceived as barriers to their disposal of their child's opioids after surgery
Disposal of unused opioids by any method
Disposal of unused opioids by any recommended or non-recommended method

Full Information

First Posted
June 19, 2018
Last Updated
March 19, 2019
Sponsor
Nationwide Children's Hospital
Collaborators
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT03575377
Brief Title
Opioid Use, Storage, and Disposal Among Pediatric Patients After Surgery
Official Title
Opioid Use, Storage, and Disposal Among Pediatric Patients After Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
June 7, 2018 (Actual)
Primary Completion Date
December 31, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nationwide Children's Hospital
Collaborators
Ohio State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Opioids are an important component of post-operative pain management among children, but are often prescribed in excess and rarely disposed of appropriately. The lack of prompt and proper opioid disposal after recovery from surgery is contributing to the opioid crisis in Ohio by placing children at risk of accidental ingestion of opioids remaining in the home and allowing for unused opioids to be diverted for non-medical use. The investigators propose to reduce the burden of the opioid crisis in Ohio by testing a strategy to increase proper opioid disposal by families of children undergoing outpatient surgery. The investigators will test the impact of a novel opioid disposal mechanism, the Deterra® drug deactivation system, after pediatric surgical operations. This system deactivates pills, liquids, or patches, allowing for their disposal in the home garbage. The investigators propose to evaluate the effectiveness of providing Deterra® bags to families of children having surgery on their disposal of excess opioids. The investigators will perform a randomized controlled trial (RCT) to test the effectiveness of Deterra® to improve opioid disposal among families of children having outpatient surgery at Nationwide Children's Hospital.
Detailed Description
Opioids are an important component of post-operative pain management among children, but are often prescribed in excess and rarely disposed of appropriately. The lack of prompt and proper opioid disposal after recovery from surgery is contributing to the opioid crisis in Ohio by placing children at risk of accidental ingestion of opioids remaining in the home and allowing for unused opioids to be diverted for non-medical use. The investigators propose to reduce the burden of the opioid crisis in Ohio by testing a strategy to increase proper opioid disposal by families of children undergoing outpatient surgery. The investigators will test the impact of a novel opioid disposal mechanism, the Deterra® drug deactivation system, after pediatric surgical operations. This system deactivates pills, liquids, or patches, allowing for their disposal in the home garbage. The investigators propose to evaluate the effectiveness of Deterra® for opioid disposal among families of Ohio children having surgery. The investigators will perform a randomized controlled trial (RCT) to test the effectiveness of Deterra® to improve proper opioid disposal among families of children having outpatient surgery at Nationwide Children's Hospital. The goal of this project is to evaluate the impact of providing the Deterra® drug deactivation system on the excess opioid disposal rate among families of children having outpatient otolaryngologic or urologic surgery at NCH. A second objective of this study is to evaluate whether the impact of the Deterra® drug deactivation system varies by parent/guardian health literacy level or signing of an "opioid consent form" acknowledging that they will follow appropriate dosing recommendations, not give opioids if their child appears sleepy, not give Tylenol concurrently with Tylenol-containing opioid medications, dispose of unused opioids safely and responsibly, and contact their child's surgeon's office or the on-call physician with any questions. To accomplish these objectives, the investigators will perform a randomized controlled trial comparing groups of patients who receive either 1) a Deterra® bag along with brief instruction on how and why to use it along with routine postoperative instructions or 2) routine postoperative instructions. The investigators plan to enroll 202 caregivers of children having outpatient surgery. All families will receive a 1-page pain journal to record the child's opioid and non-opioid adjunct pain medication administration. In addition to the instructions provided by the care team as described above, families randomized to the intervention arm will additionally receive a Deterra® bag and instructions on its use by a research team member. In order to minimize disruption to the clinical work flow, minimal data will be collected at baseline directly from enrolled families. This will include the contact information required for follow-up, a limited set of research related questions, and a brief assessment of parent/guardian health literacy. Baseline demographic and clinical characteristics of the child, such as their primary payer, residential address, age, and comorbidities at the time of surgery will be extracted from the electronic medical record. Parents/guardians will be contacted by their preferred method of email survey or phone call at 2 weeks postoperatively, at which time they will be surveyed on their child's postoperative opioid and non-opioid medication use, opioid storage location, quantity of opioid remaining, disposal method, and any barriers to disposal. If the child continues to require opioids, they will be contacted again at 4 weeks postoperatively. If the parent believes that their older child or adolescent can assist in answering the survey questions, they will be encouraged to complete the survey together. The primary outcome of this trial is the proper disposal of unused opioids. Secondary outcomes include the quantities of opioid used and leftover after surgery, opioid storage location, disposal by any method, and barriers to disposal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tonsillitis, Sleep Disordered Breathing, Hernia, Hydrocele, Hypospadias, Undescended Testicle, Circumcision

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
202 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Deterra Bag
Arm Type
Experimental
Arm Description
These families will receive a Deterra® bag (a drug Disposal Aid) and instructions on its use by a research team member.
Arm Title
Control
Arm Type
No Intervention
Arm Description
These families will receive routine postoperative instructions only.
Intervention Type
Other
Intervention Name(s)
Disposal Aid
Intervention Description
Deterra® drug deactivation system
Primary Outcome Measure Information:
Title
Proper disposal of unused opioids
Description
The proper disposal of unused opioids, defined as the disposal of unused opioids by an FDA-recommended method or by using the Deterra® drug deactivation system.
Time Frame
2-4 weeks
Secondary Outcome Measure Information:
Title
Quantity of opioid used after surgery
Description
Number of doses of opioid pain medication used after surgery
Time Frame
2-4 weeks
Title
Quantity of opioid leftover after surgery
Description
Number of doses of opioid pain medication leftover after surgery
Time Frame
2-4 weeks
Title
Proper storage of opioids
Description
Whether the opioids were properly stored after surgery
Time Frame
2-4 weeks
Title
Barriers to opioid disposal
Description
What the parent/caregiver perceived as barriers to their disposal of their child's opioids after surgery
Time Frame
2-4 weeks
Title
Disposal of unused opioids by any method
Description
Disposal of unused opioids by any recommended or non-recommended method
Time Frame
2-4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Parent or legal guardian of a child having outpatient otolaryngologic or urologic surgery at Nationwide Children's Hospital Child's age is between 1 and 17 years Child is expected to receive a discharge opioid prescription Exclusion Criteria: •Unable or unwilling to track pain medication use or complete a follow-up survey
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer Cooper, PhD
Organizational Affiliation
Research Institute at Nationwide Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jennifer Cooper
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31233129
Citation
Lawrence AE, Carsel AJ, Leonhart KL, Richards HW, Harbaugh CM, Waljee JF, McLeod DJ, Walz PC, Minneci PC, Deans KJ, Cooper JN. Effect of Drug Disposal Bag Provision on Proper Disposal of Unused Opioids by Families of Pediatric Surgical Patients: A Randomized Clinical Trial. JAMA Pediatr. 2019 Aug 1;173(8):e191695. doi: 10.1001/jamapediatrics.2019.1695. Epub 2019 Aug 5.
Results Reference
derived

Learn more about this trial

Opioid Use, Storage, and Disposal Among Pediatric Patients After Surgery

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