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Clinical Trials/NCT02485795
NCT02485795
Unknown
Not Applicable

A Multicenter Longitudinal Observational Study Evaluating Genotypic Association wIth Clinical Outcomes in Interventional Pain Management Modalities

Proove Bioscience, Inc.31 sites in 1 country50,000 target enrollmentSeptember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Proove Bioscience, Inc.
Enrollment
50000
Locations
31
Primary Endpoint
Medication dosage prescribed to the participants
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the impact of genetic testing on healthcare decisions and patient outcomes in interventional pain management clinical care. Results of genetic testing will also be compared with the clinical outcome measures collected to discover novel genetic factors that may influence patient care.

Detailed Description

Specific genetic variations have been identified that result in alteration of expression or function of receptors, enzymes, and transporters that are relevant to the safety and efficacy of a medical treatment. By providing information regarding the genetic risks and the most effective therapy for an individual patient, clinicians may improve the efficacy of treatment and decrease the risk of adverse events. The purpose of this study is to evaluate how currently available genetic tests are being implemented in various interventional pain management clinics around the United States, and whether this information results in benefits to patient care. Considering patient genotype correlates with pain sensitivity and perception, as well as autonomic nervous system dysfunction due to variations in sodium and potassium channels, genotypic associations can significantly improve outcomes in interventional pain management modalities including: * Injections (also called nerve blocks using medications), such as steroids and opioids, including epidural steroid injections, facet joint injections, single nerve root blocks, and sacroiliac joint injections; * Radiofrequency Rhizotomy (radiofrequency ablation and neuroablation), using x-ray guidance and a needle with an electrode at the tip that gets heated, to temporarily turn off a nerve's ability to send pain messages to the brain; and, * Intrathecal pump implants which provide potent medications straight to the source of pain. Patient that are receiving Proove Bioscience's genetic testing will complete validated questionnaires to measure specific outcomes related to their treatment at each clinical visit, including medication efficacy, reduction in adverse drug events, and healthcare utilization. Physicians will document any changes made to treatment regimens, including adjustments to medications or non-pharmacological treatments, and any improvements in the outcome measures. Statistical analysis will be performed to calculate relationships between genotypic and phenotypic data points collected in this study. The results of this study will provide a measurable understanding of the medical and economic value of implementing genetic testing into interventional pain management. Furthermore, data points collected will be used to examine novel correlations and associations between single nucleotide polymorphisms and longitudinal clinical outcome measures.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
August 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Proove Bioscience, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Provide signed and dated informed consent form
  • Willing to comply with all study procedures and be available for the duration of the study
  • Male or Female, at least 18 years of age
  • Currently taking or a candidate for opioid pain medication
  • Documented or recent complaint of pain within 90 days (location to be documented in the case report form) with initial date of onset

Exclusion Criteria

  • Severe hepatic or renal disease (where current pharmaceutical dosing is affected and/or requires adjustment of standard dosing prior to PGx testing)
  • Significant diminished mental capacity that is unable to understand the protocol, surveys and questionnaires; unable to read/write English or Spanish.
  • Recent febrile illness that precludes or delays participation by more than 1 month
  • Pregnancy or lactation
  • Participation in a clinical study that may interfere with participation in this study
  • Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study

Outcomes

Primary Outcomes

Medication dosage prescribed to the participants

Time Frame: 60 days

Pain Scores on the Pain Numeric Rating Scale (NRS)

Time Frame: 60 days

Number of Participants that Experience of Adverse Events

Time Frame: Up to 2 years

Severity of Adverse Events Experienced by Participants

Time Frame: Up to 2 years

Function/Disability assessment on the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

Time Frame: 60 days

Type of Adverse Events Experienced by Participants

Time Frame: Up to 2 years

Type of treatments selected for participants

Time Frame: 60 days

Self-rated response levels to prescribed medications

Time Frame: 60 days

Frequency of participant urine drug screens

Time Frame: 60 days

Secondary Outcomes

  • Assessment of previous treatments(60 days)
  • Co-occurring disorders reported by ICD-9/10 code(60 days)
  • Urine drug screen results(60 days)

Study Sites (31)

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