Pain and Medication Use Following Surgery

Completed · Not applicable

Conditions studied: Opioid Use

In brief

Patients will be randomized to one of two interventions intended to facilitate safe disposal of opioids after cessation following surgery. For pragmatic reasons, participants will be randomized by day to either the information sheet or the disposal bag using a block randomization schedule. To ensuring adequate sample size, patients will be enrolled for a \~4-week period following the 2-week usual care run in period. In the event that the sample size estimate has not been reached after the 4-week intervention period, additional patients will be enrolled accordingly.

Key facts

Study ID

NCT03179566

Run by

University of Michigan

People needed

391

Starts

2017-06-06

Expected to finish

2017-09-01

Last updated by the study team

2017-09-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Scheduled for surgery at Michigan Medicine's East Ann Arbor Ambulatory Surgery \& Medical Procedures Center

You may not qualify if…

• Unable to speak English
• Inability to understand or complete the surveys
• Other conditions that preclude meaningful participation in the study

Where it is running

• East Ann Arbor Ambulatory Surgery & Medical Procedures Center - Michigan Medicine — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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