Validation Study of Neuropathic Pain

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2010 by University of Wisconsin, Madison.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of Wisconsin, Madison
ClinicalTrials.gov Identifier:
NCT00623961
First received: February 14, 2008
Last updated: June 24, 2010
Last verified: June 2010
  Purpose

This study seeks to validate clinically evoked or obtained objective pain signs with the patient's corresponding quantified subjective pain symptoms. This will allow for validation of objective clinical pain signs to then be used to begin to classify patients with pain based on symptoms and signs. This then can be used as a basis for further study of neuropathic pain mechanisms in human patients.


Condition
Neuropathic Pain From Spinal Cord Injury
Diabetic Peripheral Neuropathy
Post Herpetic Pain

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Validation Study of Positive Phenomena in Neuropathic Pain

Resource links provided by NLM:


Further study details as provided by University of Wisconsin, Madison:

Estimated Enrollment: 180
Study Start Date: April 2007
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients with neuropathic pain from the following diagnosis groups: post-herperic neuralgia, painful diabetic neuropathy, and spinal cord injury will be included in the study if their pain is of at least 6 months duration.

Criteria

Inclusion Criteria:

  • Subjects must be 18 years of age and older, and able to provide informed consent and communicate in English. Pain rating inclusion criteria will be pain greater than 3 up to 9, as rated on the 0-10 pain scale, where 10 is the worst pain imaginable. This rating is based on the numeric pain rating scale (NPRS).
  • PHN - Subjects with PHN will have a history of pain of at least 6 months duration in the area that was the site of a zoster rash resulting in nerve injury. In most cases, subjects experience a number of sensory abnormalities in the affected area, ranging from pain to numbness, and various degrees of hypersensitivity. Subjects with PHN must otherwise be in stable health. Pain rating inclusion criteria for PHN subjects will be pain greater than 3 up to 9, as rated on the 0-10 pain scale, where 10 is the worst pain imaginable.
  • PDN - Subjects with diabetes mellitus and neuropathy who have a history of pain, predominantly in the lower extremities, of at least 6 months duration qualify for the diagnosis of PDN for purposes of this study. In most cases PDN is due to small fiber neuropathy, so physical examination should yield sensory abnormalities, such as pain, paresthesiae and numbness. Motor function and stretch reflex abnormalities are common but not necessary for inclusion. PDN patients in whom large fiber functions are affected, experience weakness and decreased or absent stretch reflexes, respectively, and are eligible for this study. Other causes of neuropathy will be excluded. PDN patients with pain rating of greater than 3 up to 9 on 0-10 scale will be included.
  • SCI pain - Subjects with SCI and pain of at least 6 months duration will be invited to participate. In most cases, these subjects' sensory, motor and stretch reflex abnormalities are consistent with SCI. Sensory findings range form complete loss of sensation to preservation of all sensory modalities. Motor findings range from mild weakness to complete paralysis. Stretch reflexes are most frequently increased though in a few patients they can be absent. Based on the constellation of sensory and motor findings in particular patients, diagnosis of complete versus incomplete SCI is made. In this study we will study patients with incomplete SCI who have pain at level of injury or below level of injury, or both. Subjects with SCI who have pain rating of greater than 3 up to 9 on 0-10 scale will be included.

Exclusion Criteria:

  • Patients with pain due to disorders other than PDN, PTN, or SCI, as well as unknown causes, will be excluded.
  • Patients with neuropathies from causes such as vasculitis, demyelinating polyneuropathies, HIV-associated neuropathy, and paraneoplastic and post-infectious neuropathies will be excluded.
  • Patients with chemotherapy-induced neuropathy will be excluded.
  • Patients who suffer from pain due to different pain mechanisms will be excluded.
  • Patients with other pain (at a different site) that is more severe than their PDN or PTN pain will be excluded.
  • Patients with a history of recent or ongoing alcohol or other drug addiction disorders (as self-reported or previously documented in the medical record) will be excluded.
  • Patients who are determined to have cognitive and reading impairments which would preclude them from completing questionnaires will be excluded.
  • Patients whose chronic medical and psychiatric comorbidities are not under optimal control, or who are currently experiencing an acute exacerbation of a medical or psychiatric comorbidity, will be excluded.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00623961

Contacts
Contact: Miroslav Backonja, MD 608-263-9550 backonja@Neurology.wisc.edu

Locations
United States, Wisconsin
UW Hospitals and Clinics Recruiting
Madison, Wisconsin, United States, 53792
Contact: Miroslav Backonja, MD    608-263-9550    backonja@neurology.wisc.edu   
Principal Investigator: Miroslav Backonja, MD         
Sponsors and Collaborators
University of Wisconsin, Madison
Investigators
Principal Investigator: Miroslav Backonja, MD University of Wisconsin, Madison
  More Information

No publications provided

Responsible Party: Miroslav Backonja, MD, University of Wisconsin
ClinicalTrials.gov Identifier: NCT00623961     History of Changes
Other Study ID Numbers: 2006-0425
Study First Received: February 14, 2008
Last Updated: June 24, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by University of Wisconsin, Madison:
Neuropathic Pain

Additional relevant MeSH terms:
Neuralgia
Peripheral Nervous System Diseases
Spinal Cord Injuries
Diabetic Neuropathies
Wounds and Injuries
Pain
Neurologic Manifestations
Nervous System Diseases
Neuromuscular Diseases
Signs and Symptoms
Spinal Cord Diseases
Central Nervous System Diseases
Trauma, Nervous System
Diabetes Complications
Diabetes Mellitus
Endocrine System Diseases

ClinicalTrials.gov processed this record on July 24, 2014