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Tracking Outcomes in Pain Patients Using Fitness Devices

NCT02420457 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2019-04-25

No results posted yet for this study

Summary

The investigators are assessing the validity of fitness devices as surrogate measures of chronic pain survey outcomes.

Conditions

Interventions

PROCEDURE

Epidural injection

After evaluation by their pain physician, if the clinician offers an epidural injection for their back pain, they will be followed for this study before and after the injection.

DRUG

Epidural steroid injection as determined by routine care provider

Betamethasone Triamcinolone Dexamethasone Methylprednisolone Lidocaine Bupivacaine Ropivacaine Normal saline

Sponsors & Collaborators

  • North Carolina Translational and Clinical Sciences Institute

    collaborator OTHER

  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Matthew C Mauck, MD PhD · Assistant Professor

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2018-05-31
Completion
2018-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02420457 on ClinicalTrials.gov