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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00695006
Other study ID # 5388642
Secondary ID
Status Active, not recruiting
Phase N/A
First received June 9, 2008
Last updated June 24, 2008
Start date September 2006
Est. completion date July 2008

Study information

Verified date June 2008
Source Rocky Mountain University of Health Professions
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To date, optimal strategies for the management of patients with Cervical Radiculopathy (CR) remain elusive. The purpose of this study was to compare the effects of manual therapy, exercise, and cervical traction to manual therapy, exercise, and sham traction on pain, function and disability in patients with CR.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 81
Est. completion date July 2008
Est. primary completion date December 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 3 of 4 positive on CPR, 18-70yrs

Exclusion Criteria:

- history of previous cervical or thoracic spine surgery

- bilateral upper extremity symptoms

- signs or symptoms of UMN disease

- medical "red flags"(tumor, fracture, rheumatoid arthritis, osteoporosis, prolonged steroid use)

- cervical spine injections (steroidal) in the past two weeks

- current use of steroidal medication prescribed for their radiculopathy symptoms

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Sham Traction
Traction <5lbs
Traction
Standard supine intermittent traction

Locations

Country Name City State
United States Advance Rehab at Fredericksburg Orthopaedics Fredericksburg Virginia

Sponsors (1)

Lead Sponsor Collaborator
Rocky Mountain University of Health Professions

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neck Disability Index 2wk, 4wk, 3mo, 6mo No
Primary Patient Specific Functional Scale 2wk, 4wk, 3mo, 6mo No
Primary Numeric Pain Rating Scale 2wk, 4wk, 3mo, 6mo No
Secondary Global Rating Of Change 2wk, 4wk, 3mo, 6mo No
Secondary Body Diagram 2wk, 4wk, 3mo, 6mo No
Secondary Fear Avoidance Belief Questionnaire 2wk, 4wk, 3mo, 6mo No
Secondary Satisfaction 2wk, 4wk, 3mo, 6mo No
Secondary Grip Strength 2wk, 4wk No
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