Risk Factors for Long-term Opioid Use

NCT ID: NCT04928131

Last Updated: 2022-04-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1500392 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-31

Study Completion Date

2021-02-28

Brief Summary

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Surgeons often see patients with pain to exclude organic pathology and consider surgical treatment. We examined factors associated with long-term opioid therapy among patients with foot/ankle, anorectal, and temporomandibular joint pain to aid clinical decision making.

Using the IBM MarketScan® Research Database, we conducted a retrospective cohort analysis of patients aged 18-64 with a clinical encounter for foot/ankle, anorectal, or temporomandibular joint pain (January 2007-September 2015). Multivariable logistic regression was used to estimate adjusted odds ratios for factors associated with long-term opioid therapy, including age, sex, geographic region, pain condition, psychiatric diagnoses, and surgical procedures in the previous year.

Detailed Description

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Conditions

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Pain Syndrome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Anorectal

Patients presenting with anorectal pain.

No intervention - retrospective observational cohort study

Intervention Type OTHER

TMJ

Patients presenting with temporomandibular joint pain.

No intervention - retrospective observational cohort study

Intervention Type OTHER

Foot/Ankle

Patients presenting with foot and ankle pain.

No intervention - retrospective observational cohort study

Intervention Type OTHER

Interventions

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No intervention - retrospective observational cohort study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18-64 years old
* at least one encounter for anorectal, foot/ankle, or TMJ pain
* Marketscan continuous enrollment for 1 year prior and 1 year after the index pain encounter
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Cindy Kin

Assistant Professor of Surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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43803

Identifier Type: -

Identifier Source: org_study_id

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