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OpenTrials
Completed

NCT Number: NCT01715766

VIPER: Veterans Integrated Pain Evaluation Research

The purpose of the study is to learn about the causes of different types of pain that can occur in people who have had an amputation. By gathering information through blood tests, photographs, a nerve test, and questionnaires, we hope to de-code how each individual's special characteristics affect the type and amount of pain they experience in their amputated limb.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Walter Reed National Military Medical Center

Bethesda, Maryland, 20889, United States

About this study

Studies have already shown that pain following amputation might be caused by differences in a person's genes. This study may help us find out how genes affect the way you feel pain and why you may feel more or less or different kinds of pain than another person with a similar amputation. What we learn in this research study may lead to discoveries as to why some painkillers work better for some people than others.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female active duty military personnel age 18 years and older undergoing treatment at WRAMC and future WRNMMC with the diagnosis of post injury amputation of 1 limb, more than 3 but less than 18 months prior to enrollment. In particular, phantom limb pain patients will be included

Exclusion criteria

  • Severe Traumatic Brain Injury (Primary major head trauma and diagnosis of traumatic brain injury resulting in documented, permanent or prolonged cognitive deficits that would preclude participation in the study (i.e. decreased intellectual capacity, marked memory deficits, or inability to communicate verbally or in writing)
  • Significant cognitive deficits that would preclude participation in the study.
  • Substantial hearing loss without alternative means of communication.
  • Documented spinal cord injury with permanent or persistent deficits.
  • Diagnosis of fibromyalgia or other chronic pain syndrome such as chronic headaches.
  • Evidence of ongoing tissue damage pain, infection, bone spur, or poorly fitting prosthesis.

Treatment and study plan

Primary outcomes

  1. Proteomics

    Time frame: 1 day

    To determine which proteins represent circulating qualitative and quantitative biomarkers of pain.

Sponsors and collaborators

Lead sponsor

Defense and Veterans Center for Integrative Pain Management

Other

Collaborators

  • Duke University

Registry information

Official study title

VIPER: Veterans Integrated Pain Evaluation Research- Molecular Subtypes of Chronic Pain Syndromes

Acronym: VIPER

Important dates

Study start
2012
Primary completion
2013
Study completion
2017
First posted
Oct 29, 2012
Registry last updated
Aug 14, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.