War Wounded, a Comparison of Two Pain Management Approaches

NCT01620411 | Withdrawn DMC

• 1 other identifier: 120565
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 1

Brief Summary

This study aims to investigate the relative effectiveness of two different pain management plans for injuries sustained while active duty in the military. One arm of the study has subjects undergo standard comprehensive medical management, while the other adds the placement of a spinal cord stimulator, a common procedure for the alleviation of pain.

Conditions

Injuries; Pain

Keywords

Active Duty; Comprehensive Medical Management; Spinal Cord Stimulator; Veteran; sustained; military

Outcome Measures

Primary Outcomes (1)

• Decreased Pain Ratings

  Pain rating using the Numeric Pain Rating Scale (NPRS) over time. The NPRS is assessing the patients pain on a 11-point rating scale from 0 - 10 with 0 being no pain at all and 10 being the worst imaginable pain. The test is self-reported and can also be administered by an interviewer.

  3 years

Study Arms (2)

Comprehensive Medical Management (CMM)

EXPERIMENTAL

This arm will receive standard of care treatment for injuries sustained while on active duty. Non-Invasive.

Other: Comprehensive Medical Management

CMM + Spinal Cord Stimulator (SCS)

EXPERIMENTAL

This arm will combine comprehensive medical management with placement of a spinal cord stimulator.

Procedure: Spinal Cord Stimulator

Interventions

Comprehensive Medical Management OTHER

Standard of care for failed back surgery syndrome sustained while on active duty, primarily focused on physical therapy, medication including: opioid analgesics, muscle relaxants, non-opioid analgesics, etc.

Comprehensive Medical Management (CMM)

Spinal Cord Stimulator PROCEDURE

This arm combines comprehensive medical management (as above) with the trial and possible eventual permenant placement of a spinal cord stimulator, a common pain management procedure.

CMM + Spinal Cord Stimulator (SCS)

Eligibility Criteria

• Age: 18 Years+
• Sex: male
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subject is a veteran or active duty service member injured while on active military duty receiving care for pain related to the injury(ies) in the Department of Defense health care system or through the Department of Veteran's Affairs.
• Subject is 18 years of age or older.
• The elapsed time since the active-duty injury leading to chronic pain is not less than 3 months.
• Subject reports constant or daily episodes of injury-related pain of at least moderate severity, graded 4 or higher on an 11-point NPRS (point estimate by subject and Investigator at time of enrolment based on overall pain or pain at a specific site). Pain may be nociceptive, neuropathic, or mixed. Phantom pain associated with amputation of an extremity or extremities is allowed.
• Attempts to control pain with commercially available systemic analgesics have not provided adequate relief, in the judgment of the managing physician and subject.
• Subject is an acceptable candidate for surgical placement of an indwelling spinal cord stimulation device.
• Subject is judged an appropriate candidate for treatment using the available techniques and interventions encompassed within the protocol's definition of comprehensive medical management.
• For the duration of the trial, subject is willing to limit interventions for control of chronic pain to those approved by the Investigator.
• The subject is judged psychologically appropriate for either treatment intervention, based on the impression of an interviewing psychologist or psychiatrist.
• Subject provides informed consent.

You may not qualify if:

• Subject experiences phantom pain associated with amputation of both an upper and lower extremity.
• Subject has headache or visceral truncal pain or other non-musculoskeletal pain as the only pain that results in constant or daily scores of ≥4 on the 11-point NPRS.
• Subject has spinal disease that would, in the judgment of the investigator, preclude placement of a spinal cord stimulator.
• Subject has ongoing chronic infection or a medical condition associated with an unacceptably increased risk of infection related to device implantation.
• Subject has a current diagnosis or history of psychosis, cognitive impairment, hallucinations, or unexplained loss of consciousness, whether or not related to a combat injury that, in the opinion of the investigator, would exclude the patient from participating in the trial.
• Subject has a cardiac pacemaker.
• Subject has any significant medical or psychiatric condition that would interfere with the conduct of the study or with the outcome measures.
• Subject is pregnant or is breast feeding.
• Subject has participated in any drug or device trial in the past 30 days.
• Subject has any planned elective or semi-elective surgery during the 6 months of the Primary Treatment Phase, including stump revisions or grafting.
• Subject has a psychological condition of great enough severity that it would unacceptably increase the medical risks associated with implantation and care of the devices required for the treatment on the CMM + SCS arm, or would likely interfere with the subject's ability to sustain participation in a research study of long duration. Investigators are encouraged to include the medical monitor and the coordinating investigator in discussions about individual candidate subjects who have psychological diagnoses as part of the polytrauma syndrome before enrollment or treatment on this protocol.

Sponsors & Collaborators

• University of California, San Diego: lead

Study Sites (1)

VA Hospital San Diego

La Jolla, California, 92093, United States

Location

Related Links

• Location of study
• Primary Investigator Profile

MeSH Terms

Conditions

Wounds and Injuries; Pain

Condition Hierarchy (Ancestors)

Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• Tobias Moeller-Bertram

  UCSD

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Clinical Professor of Anesthesiology

Study Record Dates

• First Submitted: June 13, 2012
• First Posted: June 15, 2012
• Study Start: June 1, 2012
• Primary Completion: June 1, 2016
• Study Completion: June 1, 2017
• Last Updated: August 12, 2019

Record last verified: 2019-08

Locations

US (1)