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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Withdrawn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
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Opioid Use

Eligibility Criteria

undefined - 64 Years (Child, Adult)All SexesAccepts Healthy Volunteers

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

    First Posted
    November 21, 2017
    Last Updated
    March 27, 2020
    Sponsor
    Baylor College of Medicine
    Collaborators
    Chandrakantan
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    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    Withdrawn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

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    Safe Return and Disposal of Unused Opioids

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