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The Effect of a Charcoal Deactivation Pouch on Opioid Disposal After Cesarean Delivery

Pain, Acute Clinical Trial

Official title:
The Effect of a Charcoal Deactivation Pouch on Opioid Disposal After Cesarean Delivery

Clinical Trial Summary

Background: There is scarce literature investigating how patients dispose of unused opioid supplies after their cesarean postoperative pain has faded. The Office of the Surgeon General has identified research on the prevention of opioid use disorder area as well as research on the management of pain as a "Surgeon General Priority" that needs urgent investigation. Hypothesis: At least 33% of postpartum women discharged home with an opioid prescription and a drug deactivation pouch will use the pouch to dispose of remaining opioids within 30 days of delivery. Methods: This is a prospective single arm interventional pilot study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05498025
Study type Interventional
Source Geisinger Clinic
Contact
Status Completed
Phase N/A
Start date February 21, 2023
Completion date July 29, 2023
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