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Accuracy of Point of Care (POC) or In-office Urine Drug Testing (Immunoassay) in Chronic Pain Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01052155
First Posted: January 20, 2010
Last Update Posted: October 12, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Millennium Laboratories
Information provided by:
Pain Management Center of Paducah
  Purpose
Accuracy of Point of Care (POC) or In-office Urine Drug Testing (Immunoassay) in Chronic Pain Patients: A Prospective Analysis of Immunoassay and Liquid Chromatography Tandem Mass Spectometry (LC/MS/MS)

Condition Intervention
Chronic Pain Other: Urine Drug Testing

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Accuracy of Point of Care (POC) or In-office Urine Drug Testing (Immunoassay) in Chronic Pain Patients: A Prospective Analysis of Immunoassay and Liquid Chromatography Tandem Mass Spectometry (LC/MS/MS)

Resource links provided by NLM:


Further study details as provided by Pain Management Center of Paducah:

Primary Outcome Measures:
  • Diagnostic accuracy [ Time Frame: 72 hours ]

Estimated Enrollment: 1000
Study Start Date: February 2010
Study Completion Date: June 2010
Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Urine Drug Testing
    LC/MS/MS Laboratory Evaluation
    Other Name: In-office Urine Drug Testing (Immunoassay)
Detailed Description:

Recruitment is indicated in patients with chronic pain management with or without controlled substance therapy.

This is a diagnostic accuracy study performed in an interventional pain management referral center in the United States.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with chronic pain management with or without controlled substance therapy.
Criteria

Inclusion criteria:

• Chronic pain management with or without controlled substance therapy.

Exclusion criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01052155


Sponsors and Collaborators
Pain Management Center of Paducah
Millennium Laboratories
Investigators
Principal Investigator: Laxmaiah Manchikanti, MD Ambulatory Surgery Center, Paducah
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Laxmaiah Manchikanti, MD/Medical Director, Pain Management Center of Paducah and Ambulatory Surgery Center
ClinicalTrials.gov Identifier: NCT01052155     History of Changes
Other Study ID Numbers: Protocol 26
First Submitted: January 18, 2010
First Posted: January 20, 2010
Last Update Posted: October 12, 2017
Last Verified: March 2011

Keywords provided by Pain Management Center of Paducah:
Controlled substances
Opioids
Benzodiazepines
Illicit drugs
Immunoassay drug testing
Point of care (POC) testing
Liquid Chromatography Tandem Mass Spectometry

Additional relevant MeSH terms:
Chronic Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms