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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06215170
Other study ID # SafeMedWasteCT2023
Secondary ID 1R43DA057750-01A
Status Not yet recruiting
Phase Phase 1
First received
Last updated
Start date February 1, 2024
Est. completion date February 1, 2025

Study information

Verified date January 2024
Source SafeMedWaste, Inc.
Contact Justin Stas, B.S Biomedical Engineering
Phone 9011340
Email jstas@safemedwaste.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is an urgent unmet medical need for a cost-effective, environmentally friendly, in-home opioid disposal solution for surgical patients that is clinically proven to reduce opioid use disorder that is substantiated with economic data. SafeMedWaste, Inc. (SMW) has developed the patented SafeMedWaste in-home drug disposal container, that completely destroys opioids within minutes and can be placed in the regular trash, without risk of ground or municipal water contamination. A pilot randomized clinical trial will evaluate the use of SafeMedWaste in 300 adult patients in outpatient surgery clinics undergoing shoulder and knee surgery.


Description:

The trial will evaluate opioid disposal rates and events related to opioid diversion and use disorder in 300 adult patients 18 years of age and older undergoing outpatient knee and shoulder surgery who are prescribed opioids to manage their acute post-surgical pain. Patients will be randomized into two arms. During the standard of care post op visits (2-, 6- and 10- weeks), when the treating physician has determined that the patient will no longer need opioids to manage their post-surgical pain, all patients will receive general instructions by video on opioid disposal recorded by one of the orthopedic surgeons. Patients in the treatment arm will also be given the SafeMedWaste opioid disposal system and watch an instructional video on how to use the product. All patients will complete a pre-surgery survey and a post-surgery survey 90 days after surgery. Patients will self-report their disposal or non-disposal of the drugs, documented with pictures uploaded to the patient's MyChart account. Data from the surveys will be statistically analyzed to identify significant factors that influenced patients' behavior vis-à-vis opioid disposal.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 300
Est. completion date February 1, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Inclusion Criteria: - Subject is 18 + years of age - Subject is opioid naive (within the last 3 months), as evidenced by MyChart patient record or response to medical history questions - Subject is scheduled to undergo shoulder and/or knee surgery Exclusion Criteria: - Subject has a history of opioid addiction, as evidenced by MyChart patient record or response to medical history questions - Subject is currently utilizing prescription narcotics for any reason, as evidenced by MyChart patient record or response to medical history questions - Subject does not have the mental capacity to make their own healthcare decisions - Subject is unable to provide written consent

Study Design


Related Conditions & MeSH terms


Intervention

Device:
SafeMedWaste
SafeMedWaste opioid disposal kit

Locations

Country Name City State
n/a

Sponsors (4)

Lead Sponsor Collaborator
SafeMedWaste, Inc. National Institute on Drug Abuse (NIDA), Prisma Health-Midlands, University of South Carolina

Outcome

Type Measure Description Time frame Safety issue
Other Reasons for disposal/non- disposal Reasons why the patient chose to dispose of opioids or chose not to, as reported in the post- surgery survey, will be statistically analyzed and correlated as appropriate to other data. Within 3 months following surgery
Other Time of disposal When the patients dispose of opioids, as reported by patients in post-surgery survey and/or documented with pictures in MyChart, will be tracked up to 3 months post-surgery. Within 3 months following surgery
Other Amount of opioids used The amount of opioids used will be tracked at visit weeks 2, 6 and 10, post surgery, through clinic pill counts, or as self-reported by patients up to 3 months. Within 3 months following surgery
Other Opioid Use Disorder (OUD) Any OUD reported in the patient medical record will be tracked up to 3 months following surgery. Within 3 months following surgery
Other Diversion event Any diversion event as described by patient at clinical visit or in post-surgery survey will be recorded. Within 3 months following surgery
Other Pre-Surgery Survey Pre-Surgery Survey, see Ex. 1, Protection of Human Subjects, will be completed by patients at enrollment. Questions include patient past surgical experience and attitudes toward pain. Data will be recorded in REDCap and statistically analyzed. At enrollment
Other Post-Surgery Survey Patients will answer post-surgery survey, see Ex. 2, Protection of Human Subjects, within 3 months following surgery. Questions include pain experiences from their surgery and disposal compliance. Data will be recorded in REDCAP and statistically analyzed for correlations of patient attitudes toward and experience with pain and other factors to disposal compliance to create clinician/patient education protocols to be studied in future trial. 3 months following surgery
Other Provider Satisfaction Survey Provider participants will answer Provider Satisfaction survey, see Ex. 4, Protection of Human Subjects, upon study completion. Data will be recorded in REDCap and statistically analyzed. Upon study completion
Primary Opioid disposal compliance Opioid disposal compliance will be tracked up to 3 months post-surgery, as reported by patients in post-surgery survey and/or documented with pictures uploaded by patient to MyChart. Within 3 months following surgery
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