Actively Recruiting

Age: 18Years +
All Genders
NCT06288256

Neurocognitive and Genomic Predictors of Persistent Pain and Opioid Misuse After Spine Surgery

Led by Icahn School of Medicine at Mount Sinai · Updated on 2024-10-16

60

Participants Needed

1

Research Sites

170 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Having spine surgery and recovery is a vulnerable period when opioid naive patients may transition into long-term use of opioids, and when previously opioid tolerant patients may be at risk to continue towards long-term opioid use and dependence. However, little is known about risk for developing opioid misuse, taking opioids differently than indicated or prescribed, and later OUD. This study addresses the question of whether behavior, cognitive features, and genomic markers can predict misuse of opioids, persistent pain and disability in individuals after spine surgery. To determine if impulsivity, inhibitory control, drug choice, and/or cognitive distortions predict opioid misuse and disability in spine surgery patients with differential gene expression. This is a prospective observational longitudinal study characterizing behavioral phenotypes in adults undergoing spine surgery using both patient-reported survey measures, cognitive testing and blood sampling. Outcome measures include correlations between impulsivity measures, opioid drug choice responses and cognitive distortion scores, and opioid misuse with spine related disability, and gene expression counts.

CONDITIONS

Official Title

Neurocognitive and Genomic Predictors of Persistent Pain and Opioid Misuse After Spine Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18
  • Diagnosed with lumbar, cervical, or thoracic spine pathology
  • Scheduled to undergo elective spine surgery with or without instrumentation
Not Eligible

You will not qualify if you...

  • Severe psychiatric condition interfering with study participation
  • Major cardiac, pulmonary, renal, infectious, or hepatic condition interfering with study participation
  • Polytrauma
  • Prolonged hospitalization longer than 10 days
  • Pregnancy
  • Known surgery cancellation within study period

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mount Sinai Spine Center

New York, New York, United States, 10029

Actively Recruiting

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Research Team

C

Chinwe Nwaneshiudu, MD PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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