Last reviewed · How we verify

NCT05498025

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

Completed NA Last updated 19 January 2024
What this trial tests

NA trial testing Deterra activated charcoal pouch in Pain, Acute in 37 participants. Completed in 29 July 2023.

Timeline
21 February 2023
Primary endpoint
29 July 2023
29 July 2023

Quick facts

Lead sponsorGeisinger Clinic
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment37
Start date21 February 2023
Primary completion29 July 2023
Estimated completion29 July 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Geisinger Clinic

Who can join

Adults 18 to 55, female only, with Pain, Acute or Opioid Misuse. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Pain, Acute

Currently open trials in the same condition.

Other Geisinger Clinic trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05498025.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing