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NCT03285061 Clinical Trial

Excess Opioid Disposal Following Orthopedic Foot and Ankle Surgery

Behavior Clinical Trial

Official title:
Excess Opioid Disposal Following Orthopedic Foot and Ankle Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03285061
Other study ID # 2017P002031
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2017
Est. completion date July 1, 2019

Study information
Verified date January 2021
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to survey the drug disposal methods of orthopedic foot and ankle patients with excess pain medication following and operation. The study is a randomized control trial comparing the use of FDA approved at home disposal methods to current clinical methods of recommending disposal at medication drop off locations.

Recruitment information / eligibility
Status Completed
Enrollment 75
Est. completion date July 1, 2019
Est. primary completion date July 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - This study will include foot and ankle orthopedic patients at Brigham and Women's Hospital undergoing a surgical procedure. Exclusion Criteria: - Those under age 18 will be excluded from this study, as their variation in care could affect the data. We will also exclude adults with impaired decision-making capacity and adults who take methadone or have a history of prior opioid dependence.

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Deterra Drug Deactivation System
A portable bag that will neutralize and dissolve excess medication, rendering it completely unusable and safe for landfill disposal. The system meets FDA and DEA standards for at home disposal systems.

Locations
Country Name City State
United States Brigham and Women's Hospital Boston Massachusetts

Sponsors (1)
Lead Sponsor Collaborator
Brigham and Women's Hospital

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Participants Who Safely Disposed The Excess Medication Patients will be given a survey to obtain their method of disposal for excess post-operative pain medication. 6 weeks
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