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Risk of Shopping Behavior of Tapentadol Immediate-Release (IR) Compared to Oxycodone Immediate-Release (IR)

Risk of Shopping Behavior of Tapentadol IR Immediate-Release (IR) Compared to Oxycodone IR Immediate-Release (IR)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01545778
Enrollment
646620
Registered
2012-03-07
Start date
2010-02-28
Completion date
2012-02-29
Last updated
2012-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Abuse Detection

Keywords

Substance abuse detection, Opioids abuse, Tapentadol immediate-release (IR), Oxycodone immediate-release (IR)

Brief summary

The purpose of this study is to compare the risk of shopping behavior of tapentadol immediate release with the risk of shopping behavior of oxycodone immediate release.

Detailed description

This is a retrospective (a study that looks backward in time, usually using medical records and interviews with patients) matched cohort (designated group followed or traced over a period of time) study using IMS LRx database. This database covers 65% of all retail prescriptions in the United States and includes mail service and specialty pharmacy provider prescriptions independent of the method of payment. The study will include Opioid naive patients exposed to tapentadol immediate release (IR) or oxycodone IR from July 2009 to December 2010. A naive patient is a patient who has not received an opioid of any type in the 3 months before the index date. The index date is the date of the first prescription for tapentadol IR or oxycodone IR after June 30, 2009. Patients will be followed for 1 year from their index dates. Each tapentadol IR-exposed patient will be matched to up to 4 oxycodone IR-exposed patients. Matching will allow to control in the design for potential confounding variables such as time of the exposure, geographic area, specialty of the prescriber, and age. These are variables that have been related with the risk of shopping behavior or abuse.

Interventions

Opioid naive patients exposed to tapentadol IR from July 2009 to December 2010.

Opioid naive patients exposed to Oxycodone IR from July 2009 to December 2010.

Sponsors

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Opioid naive patients (a patient who has not received an opioid of any type in the 3 months before the index date) exposed to tapentadol IR or oxycodone IR from July 2009 to December 2010 \[The index date is the date of the first prescription for tapentadol IR or oxycodone IR after June 30, 2009\]

Exclusion criteria

* Patients with use of any opioid 3 months before the index date * Patients who within 4 days on or after the index date fill a prescription for a different opioid * Patients who within 4 days on or after the index date fill a prescription for the same opioid but written by a different prescriber

Design outcomes

Primary

MeasureTime frame
Proportion of patients who developed shopping behavior defined as patients with prescriptions with at least one day of overlap, written by ≥ 2 different prescribers and filled in 3 or more pharmacies12 months

Secondary

MeasureTime frameDescription
Time to first episode of shopping behavior12 months
The number of shopping episodes during the year of follow up12 months
The type of dispensing in the first episode of shopping event12 monthsThe type of dispensing in the shopping event will be classified as Only the indexed opioid Indexed opioid was involved, or Indexed opioid was not involved at all.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026