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Clinical Study to Evaluate Clinical Impact of PGx-Guided Treatment for Patients Undergoing Elective Spinal Surgical Procedures

Primary Purpose

Acute Pain, Surgery

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
NeuroIDgenetix Test Panel
Sponsored by
AltheaDx
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Acute Pain focused on measuring PGx, pharmacogenetic testing, IDgenetix, Pain Management, AltheaDx, Post-Operative Pain Management

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female subjects over the age of 18;
  • Patients undergoing an elective spine surgical procedures
  • Willing and able to comply with study procedures
  • Able to provide written informed consent
  • Surgery timing - scheduled to occur after PGx testing and IDgenetix test report review (at least 4 days after Pre-Op visit)

Exclusion Criteria:

  • Unwilling or unable to provide written informed consent and to comply with study procedures
  • Any subject for whom providing a buccal swab sample would be contraindicated or not possible
  • Subject with a history of chronic renal dysfunction, Chronic Kidney Disease (Stage 4 or 5)
  • abnormal hepatic function within the last 2 years (INR >1.2 not attributable to anticoagulant medications, AST/aspartate aminotransferase or ALT/alanine aminotransferase >1.5x normal, or suspected cirrhosis)
  • a history of malabsorption (short gut syndrome)
  • any gastric or small bowel surgery less than 3 months prior to study enrollment
  • Patients with a significant unstable medical condition or life threatening disease
  • History of prior pharmacogenetic testing

Sites / Locations

  • Ochsner Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

NeuroIDgenetix Test Panel Intervention

Control

Arm Description

The medical provider for the NeuroIDgenetix-guided group will make post-operative pain management recommendations based on test results. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.

The medical provider for the control group will not receive the NeuroIDgenetix Test Panel results and will make post-operative pain management recommendations based as usual. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.

Outcomes

Primary Outcome Measures

Comparison of length of post-surgical hospital stay between the two treatment arms.
Duration of the post-surgical hospital stay
Comparison of patient well being between the two treatment arms as measured by pain scores
Comparison of patient well being between the two treatment arms as measured by pain scores.
Comparison of patient well being between the two treatment arms as measured by disability scores
Comparison of patient well being between the two treatment arms as measured by disability scores.

Secondary Outcome Measures

Comparison of post-operative narcotic consumption between the two treatment arms
Comparison of post-operative narcotic consumption between the two treatment arms
Comparison of opioid-related adverse effects between the two treatment arms
Comparison of opioid-related adverse effects between the two treatment arms
Comparison of time to mobilization between the two treatment arms
Comparison of time to mobilization between the two treatment arms

Full Information

First Posted
October 23, 2015
Last Updated
July 5, 2018
Sponsor
AltheaDx
Collaborators
Ochsner Health System
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1. Study Identification

Unique Protocol Identification Number
NCT02599870
Brief Title
Clinical Study to Evaluate Clinical Impact of PGx-Guided Treatment for Patients Undergoing Elective Spinal Surgical Procedures
Official Title
Prospective Randomized Clinical Study to Evaluate the Clinical Impact of Pharmacogenetics-Guided Treatment for Patients Undergoing Elective Spinal Surgical Procedures
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Terminated
Study Start Date
September 2015 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AltheaDx
Collaborators
Ochsner Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effect of pharmacogenetic (PGx) guided treatment when implemented into the pre-operative process for patients undergoing an elective spinal surgical procedure and requiring post-operative acute pain management, as compared to a group of subjects with the same attributes without the guidance of PGx testing for their post-surgery pain management. This study will also evaluate whether PGx testing can reduce narcotic consumption, opioid-related adverse effects, time to mobilization, medical visits and costs.
Detailed Description
The incidence of opioid related adverse drug events can reach as high as 50% in surgical patients and poor pain management is a significant risk factor for early readmission. In addition, the rate of non- response to certain analgesics is double in patients who are poor metabolizers as demonstrated by mutations in both CPY26d alleles. Finally, there is a growing body of literature that ineffective acute pain management contributes significantly to the risk of chronic pain syndromes. Genetics and drug interactions can alter both the pharmacokinetics and pharmacodynamics of a multitude of drug compounds and in turn influence both the safety and efficacy of selected therapeutic regimens. Pharmacogenetic-guided therapy selection can enhance patient response by facilitating the selection of the most appropriate medication at the most effective dose in the shortest possible time. In this prospective, randomized, single-blind study, the investigators will evaluate the clinical impact of pharmacogenetics-guided treatment on the duration of the post-surgical hospital stay and on patient well-being as determined by post-op pain assessments. Additionally, the impact of PGx-guided treatment on narcotic consumption, number of adverse events, re-admission rates and costs will be evaluated during the study duration.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Pain, Surgery
Keywords
PGx, pharmacogenetic testing, IDgenetix, Pain Management, AltheaDx, Post-Operative Pain Management

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NeuroIDgenetix Test Panel Intervention
Arm Type
Experimental
Arm Description
The medical provider for the NeuroIDgenetix-guided group will make post-operative pain management recommendations based on test results. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The medical provider for the control group will not receive the NeuroIDgenetix Test Panel results and will make post-operative pain management recommendations based as usual. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.
Intervention Type
Genetic
Intervention Name(s)
NeuroIDgenetix Test Panel
Other Intervention Name(s)
IDgenetix Neuro Test, PGx Testing
Intervention Description
The NeuroIDgenetix Test Panel is used to make recommendations on post-operative pain medication therapy that may be impacted by the genetic background of the patient.
Primary Outcome Measure Information:
Title
Comparison of length of post-surgical hospital stay between the two treatment arms.
Description
Duration of the post-surgical hospital stay
Time Frame
From date of surgery until hospital discharge, assessed up to 3 months
Title
Comparison of patient well being between the two treatment arms as measured by pain scores
Description
Comparison of patient well being between the two treatment arms as measured by pain scores.
Time Frame
3 months
Title
Comparison of patient well being between the two treatment arms as measured by disability scores
Description
Comparison of patient well being between the two treatment arms as measured by disability scores.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Comparison of post-operative narcotic consumption between the two treatment arms
Description
Comparison of post-operative narcotic consumption between the two treatment arms
Time Frame
3 months
Title
Comparison of opioid-related adverse effects between the two treatment arms
Description
Comparison of opioid-related adverse effects between the two treatment arms
Time Frame
3 months
Title
Comparison of time to mobilization between the two treatment arms
Description
Comparison of time to mobilization between the two treatment arms
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female subjects over the age of 18; Patients undergoing an elective spine surgical procedures Willing and able to comply with study procedures Able to provide written informed consent Surgery timing - scheduled to occur after PGx testing and IDgenetix test report review (at least 4 days after Pre-Op visit) Exclusion Criteria: Unwilling or unable to provide written informed consent and to comply with study procedures Any subject for whom providing a buccal swab sample would be contraindicated or not possible Subject with a history of chronic renal dysfunction, Chronic Kidney Disease (Stage 4 or 5) abnormal hepatic function within the last 2 years (INR >1.2 not attributable to anticoagulant medications, AST/aspartate aminotransferase or ALT/alanine aminotransferase >1.5x normal, or suspected cirrhosis) a history of malabsorption (short gut syndrome) any gastric or small bowel surgery less than 3 months prior to study enrollment Patients with a significant unstable medical condition or life threatening disease History of prior pharmacogenetic testing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wale Sulaiman, MD
Organizational Affiliation
Ochsner Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ochsner Health System
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States

12. IPD Sharing Statement

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Clinical Study to Evaluate Clinical Impact of PGx-Guided Treatment for Patients Undergoing Elective Spinal Surgical Procedures

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