Clinical Trials Directory

Trials / Completed

CompletedNCT02130258

Somatosensory Profiling in Radicular Pain Patients And it's Correlation With Treatment Outcome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
Massachusetts General Hospital · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The investigators hypothesize that there may exist different quantitative sensory profiles between radicular pain patients who respond and those who do not respond to the standard therapy of epidural steroid injections (ESI).

Detailed description

The investigators are comparing warm/cold sensation, heat/cold pain threshold, heat/cold pain tolerance, wind-up, and conditioned pain modulation (CPM) as measured by Quantitative Sensory Testing (QST) between subjects with a radicular pain condition. The investigators are comparing those who respond and those who do not respond to standard therapy (ESI) before and after the treatment.

Conditions

Interventions

TypeNameDescription
DEVICEQuantitative Sensory Testing (QST)Subjects will undergo hot and cold temperature testing using the QST device at two points: 1) Before ESI and 2) after ESI.
PROCEDUREEpidural Steroid Injection (ESI)Subjects will receive an ESI by their clinical physician as part of their clinical treatment. This procedure is not given as part of the research study.

Timeline

Start date
2012-05-01
Primary completion
2016-12-01
Completion
2017-12-01
First posted
2014-05-05
Last updated
2018-02-08
Results posted
2018-02-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02130258. Inclusion in this directory is not an endorsement.