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Investigation of Hypermobility, Biomarkers, and Pain Generators in Chronic Pain Patients

TerminatedNCT02761928
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Observational study of axial spine pain and hyperflexibility. Patients will receive physical exam maneuvers (traditional straight leg raise, FABER, facet loading as well as Beighton's hypermobility score) and blood / urine / saliva collection. They will also be separated into pain groups based on their response to injections. A correlation between exam findings and procedure group will be measured.

Study details

Official title
Investigation of Hypermobility, Biomarkers, and Pain Generators in Chronic Pain Patients
Conditions
Interventions
  • Other: Beighton score for hypermobility
Sponsor
The University of Texas Health Science Center, Houston
Start date
2016-01
Primary completion
2017-08-01
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Clinical diagnosis of axial back pain (neck, mid-back, lower back) or pain radiating to the extremity, with suspected diagnosis of a specific pain generator amenable to a pain procedure, including disorders of the nerves, joints, and muscles as listed immediately below. * Clinical decision to schedule patient for a pain procedure, including procedures targeting the following disorders: * Facet arthropathy: intra-articular facet joint injection, medial branch block, medial branch radiofrequency ablation * Sacroiliac joint dysfunction: sacroiliac joint injection, lateral branch block, lateral branch radiofrequency ablation * Myofascial pain syndrome: trigger point injection * Radiculopathy, spinal stenosis, or herniated nucleus pulposus: epidural steroid injection, selective nerve root block * Piriformis syndrome: piriformis injection * Greater trochanteric bursitis: greater trochanteric bursa injection * Able to provide HIPAA authorization to share prior medical records/imaging. Exclusion Criteria: * Previous diagnosis of cancer. * Currently pregnant. * Previously enrolled for the same procedure or the same pain generator site. (For example, this would exclude a patient who had an intra-articular facet joint injection at the right L5/S1 if: 1) he had the same injection 3 months ago and was enrolled at that time, or 2) the patient was already enrolled for a medial branch block at the right L5 and sacral ala, as this targets the same facet joint.) * Inability or unwillingness of subject or legal guardian/representative to give informed consent (e.g., ward of the state)

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02761928