Safe Return and Disposal of Unused Opioids
Primary Purpose
Opioid Use, Opioid Dependence, Opioid Abuse, Unspecified
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Opioid Return
Sponsored by
About this trial
This is an interventional prevention trial for Opioid Use
Eligibility Criteria
Inclusion Criteria:
- All patients being prescribed opioids at discharge in the Clinical Care Center/Wallace Tower Surgical Center or at the Woodlands Campus who have undergone a surgical procedure.
Exclusion Criteria:
- Parental Refusal to participate Patients not being prescribed opioids for discharge Patients on chronic opioid therapy/chronic pain patients International patients returning abroad (these takeaway envelopes are only paid through the 50 US states, DC and Puerto Rico)
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Opioids Prescribed
Arm Description
Each participant in the study will be given an envelope for return of unused opioids. The percentage of returned number of opioids will be calculated based on the number prescribed
Outcomes
Primary Outcome Measures
% of prescribed unused opioids returned
Calculate the percentage of opioids that are prescribed that are safely returned by participants and their families
Secondary Outcome Measures
Full Information
NCT ID
NCT03352479
First Posted
November 21, 2017
Last Updated
March 27, 2020
Sponsor
Baylor College of Medicine
Collaborators
Chandrakantan
1. Study Identification
Unique Protocol Identification Number
NCT03352479
Brief Title
Safe Return and Disposal of Unused Opioids
Official Title
Keeping Your Children and Home Safe Through Return and Disposal of Unused Opioids
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Withdrawn
Why Stopped
this is an observational project and doesn't not meet any of the four criteria required for listing on clinical trials.gov
Study Start Date
December 1, 2017 (Anticipated)
Primary Completion Date
June 30, 2018 (Anticipated)
Study Completion Date
July 30, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baylor College of Medicine
Collaborators
Chandrakantan
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
The opioid epidemic in the United States has become a clear health and safety concern for our children and families. Opioids given to our patients for the treatment of pain that go unused after the immediate post operative period pose a major hazard when left in the home unattended. Opioids can be accidentally ingested by small children or deliberately ingested by pre-teens and adolescents leading to major morbidity and or death. Additionally, studies have shown that many people addicted to opioids/narcotics have become so due to ingestion of medically prescribed drugs. Finally, there has been an increase number of home robberies specifically with the intent to steal prescription drugs. Removal of unused medication from the home is an important public safety concern to protect our patients, families and friends. The Sharps Co (R), offers a product called Takeaway Medication Recovery System. This product allows individuals to put unused opioids in a pre-paid envelope which is returned to the company through the postal system and properly incinerated. This provides safe disposal in accordance with the Environmental Protection Agency (EPA) to protect the water table from contamination by drugs disposed of my other means. This system through the Sharps Co would allow for de-identified tracking of returned drugs.
Detailed Description
Participants identified by the PI and participating research staff/coordinators that will receive opioids following discharge will be approached. The participant information sheet will be provided to the parents/legal guardian and explained. The consenting study coordinator will review the potential risks of opioids as described in the information sheet. A brief demonstration of the TakeAway envelope will be provided. The participants will be instructed that there is absolutely no cost to them or their family and that the envelope is pre-paid and that all returned or unreturned contents are strictly confidential. A few brief demographic questions will be asked and are completely optional. The participant will be asked for an email and contacted 15 days and 30 days following the procedure. The email will strictly be a reminder to return all un-used medication using the provided envelope Or an optional response reporting nothing to return. If participants do not have an email or do not wish to be contacted, they may still enroll in the study. The entire peri-operative period will progress in the usual manner.
Each envelope has a serial number that will be recorded during enrollment - the company provides access to ascertain exactly how many pills are returned. This access is strictly provided to the PI. The company will have no patient information and therefore only the PI will be able to track the serial number to the patient. The PI and research staff will record the number of pills prescribed to the patient to allow the research team to calculate the percentage of pills returned.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use, Opioid Dependence, Opioid Abuse, Unspecified
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Each participant will be given on envelope to return unused opioids
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Opioids Prescribed
Arm Type
Other
Arm Description
Each participant in the study will be given an envelope for return of unused opioids. The percentage of returned number of opioids will be calculated based on the number prescribed
Intervention Type
Other
Intervention Name(s)
Opioid Return
Intervention Description
Calculate the percentage of prescribed to returned opioids
Primary Outcome Measure Information:
Title
% of prescribed unused opioids returned
Description
Calculate the percentage of opioids that are prescribed that are safely returned by participants and their families
Time Frame
six months
10. Eligibility
Sex
All
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All patients being prescribed opioids at discharge in the Clinical Care Center/Wallace Tower Surgical Center or at the Woodlands Campus who have undergone a surgical procedure.
Exclusion Criteria:
Parental Refusal to participate Patients not being prescribed opioids for discharge Patients on chronic opioid therapy/chronic pain patients International patients returning abroad (these takeaway envelopes are only paid through the 50 US states, DC and Puerto Rico)
12. IPD Sharing Statement
Citations:
PubMed Identifier
32051219
Citation
Adler AC, Yamani AN, Sutton CD, Guffey DM, Chandrakantan A. Mail-Back Envelopes for Retrieval of Opioids After Pediatric Surgery. Pediatrics. 2020 Mar;145(3):e20192449. doi: 10.1542/peds.2019-2449. Epub 2020 Feb 12.
Results Reference
derived
Learn more about this trial
Safe Return and Disposal of Unused Opioids
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