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Conservative Therapy Versus Epidural Steroids for Cervical Radiculopathy

Primary Purpose

Cervical Radiculopathy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Gabapentin and/or Nortriptyline, Physical therapy
Epidural Steroid Injections (ESI)
Combination treatment
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervical Radiculopathy focused on measuring epidural steroid injection, neck pain, pharmacotherapy, radiculopathy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Cervical radicular pain based on history and physical exam (e.g. pain radiating into one or both extremities, sensory loss, muscle weakness, Spurling's test etc.)
  2. NRS arm pain score > 3
  3. MRI evidence of disc pathology consistent with symptoms

Exclusion Criteria:

  1. Untreated coagulopathy
  2. Previous spine surgery
  3. No MRI study
  4. Arm pain > 4 years duration
  5. Epidural steroid injection within past 3 years
  6. Radiculopathy not resulting from disc pathology (e.g. foraminal stenosis or tumor)
  7. Signs or symptoms or myelopathy or spinal cord compression
  8. Previous failed trials with gabapentin or pregabalin, and nortriptyline or amitriptyline
  9. Allergic reactions to gabapentin or nortriptyline
  10. Referrals from surgery for diagnostic injections for surgical evaluation
  11. Serious medical (e.g. congestive heart failure) or psychiatric (untreated depression) condition that might preclude optimal outcome
  12. Pregnancy

Sites / Locations

  • Walter Reed Army Medical Center
  • Johns Hopkins Medical Institutions

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Conservative treatment

Epidural Steroids

Combination Treatment

Arm Description

Pharmacotherapy with nortriptyline and/ or gabapentin, physical therapy (e.g. range of motion, therapeutic massage, strengthening exercises), and possibly others (e.g. acupuncture)

A series of up to 3 epidural steroid injections (ESI)with depo-methylprednisolone

These patients will receive both treatments. They can have up to 3 epidural steroid injections (ESI) with depo-methylprednisolone, and conservative treatment (i.e. pharmacotherapy with nortriptyline and/ or gabapentin, and physical therapy)

Outcomes

Primary Outcome Measures

numerical rating scale (NRS) arm pain scores
arm pain on a 0-10 scale

Secondary Outcome Measures

NRS Arm pain
0-10 scale
NRS arm pain
0-10 scale
NRS neck pain
0-10 scale
NRS neck pain
0-10 scale
NRS neck pain
0-10 scale
medication reduction
Cessation of non-opioid analgesic and/ or > 20% decrease in opioid consumption
Global perceived effect
categorical variable assessing "satisfaction" with treatment

Full Information

First Posted
June 14, 2010
Last Updated
April 23, 2014
Sponsor
Johns Hopkins University
Collaborators
Walter Reed Army Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01144923
Brief Title
Conservative Therapy Versus Epidural Steroids for Cervical Radiculopathy
Official Title
Randomized, Comparative-effectiveness Study Comparing Epidural Steroid Injections to Conservative Management With Medications and Physical Therapy in Patients With Cervical Radiculopathy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
Collaborators
Walter Reed Army Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The main objective of this study is to determine whether interventional treatment (i.e. epidural steroids), conservative therapy, or the combination, is superior for cervical radiculopathy. One hundred and sixty eight patients with radicular neck pain will be randomized in a 1:1:1 ratio to receive either cervical epidural steroid injections (CESI), non-interventional management with physical therapy and medications, or a combination of the two. The first follow-up visit will be at 1-month. In patients who obtain some benefit but continue to report significant pain, either a 2nd CESI can be done, the patient's medications can be adjusted, or both in the combination group. Those patients who fail to obtain any benefit will exit the study to receive another treatment or alternative care. The second follow-up visit will be at 3-months. Similar to the 1-month follow-up, the doctor may elect to change nothing in patients who are satisfied, adjust medications, schedule the patient for another CESI, or do both in the combination group. Patients who fail to obtain any benefit can exit the study to receive alternative treatment. The final follow-up visit will be at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Radiculopathy
Keywords
epidural steroid injection, neck pain, pharmacotherapy, radiculopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
169 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conservative treatment
Arm Type
Active Comparator
Arm Description
Pharmacotherapy with nortriptyline and/ or gabapentin, physical therapy (e.g. range of motion, therapeutic massage, strengthening exercises), and possibly others (e.g. acupuncture)
Arm Title
Epidural Steroids
Arm Type
Experimental
Arm Description
A series of up to 3 epidural steroid injections (ESI)with depo-methylprednisolone
Arm Title
Combination Treatment
Arm Type
Experimental
Arm Description
These patients will receive both treatments. They can have up to 3 epidural steroid injections (ESI) with depo-methylprednisolone, and conservative treatment (i.e. pharmacotherapy with nortriptyline and/ or gabapentin, and physical therapy)
Intervention Type
Other
Intervention Name(s)
Gabapentin and/or Nortriptyline, Physical therapy
Intervention Description
Nortriptyline up to 125 mg po qhs, and / or Gabapentin up to 1200 mg po q8h, Physical therapy (e.g. range of motion, strengthening, therapeutic massage, TENS)
Intervention Type
Procedure
Intervention Name(s)
Epidural Steroid Injections (ESI)
Intervention Description
Series of up to 3 cervical epidural steroid injections (ESI) with depo-methylprednisolone
Intervention Type
Other
Intervention Name(s)
Combination treatment
Intervention Description
Series of up to 3 cervical epidural steroid injections with depo- methylprednisolone plus Nortriptyline up to 125 mg po qhs and /or Gabapentin up to 1200 mg po q8h, and Physical therapy (e.g. TENS, exercise, range of motion)
Primary Outcome Measure Information:
Title
numerical rating scale (NRS) arm pain scores
Description
arm pain on a 0-10 scale
Time Frame
1 month after treatment
Secondary Outcome Measure Information:
Title
NRS Arm pain
Description
0-10 scale
Time Frame
3 months
Title
NRS arm pain
Description
0-10 scale
Time Frame
6 months
Title
NRS neck pain
Description
0-10 scale
Time Frame
1- month
Title
NRS neck pain
Description
0-10 scale
Time Frame
3 months
Title
NRS neck pain
Description
0-10 scale
Time Frame
6 months
Title
medication reduction
Description
Cessation of non-opioid analgesic and/ or > 20% decrease in opioid consumption
Time Frame
1-6 months
Title
Global perceived effect
Description
categorical variable assessing "satisfaction" with treatment
Time Frame
1-6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cervical radicular pain based on history and physical exam (e.g. pain radiating into one or both extremities, sensory loss, muscle weakness, Spurling's test etc.) NRS arm pain score > 3 MRI evidence of disc pathology consistent with symptoms Exclusion Criteria: Untreated coagulopathy Previous spine surgery No MRI study Arm pain > 4 years duration Epidural steroid injection within past 3 years Radiculopathy not resulting from disc pathology (e.g. foraminal stenosis or tumor) Signs or symptoms or myelopathy or spinal cord compression Previous failed trials with gabapentin or pregabalin, and nortriptyline or amitriptyline Allergic reactions to gabapentin or nortriptyline Referrals from surgery for diagnostic injections for surgical evaluation Serious medical (e.g. congestive heart failure) or psychiatric (untreated depression) condition that might preclude optimal outcome Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven P Cohen, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Salim Hayek, MD, PhD
Organizational Affiliation
Case Western
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rick Fisher, MD
Organizational Affiliation
Walter Reed National Military Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Walter Reed Army Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20307
Country
United States
Facility Name
Johns Hopkins Medical Institutions
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18204398
Citation
Hogg-Johnson S, van der Velde G, Carroll LJ, Holm LW, Cassidy JD, Guzman J, Cote P, Haldeman S, Ammendolia C, Carragee E, Hurwitz E, Nordin M, Peloso P; Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. The burden and determinants of neck pain in the general population: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Spine (Phila Pa 1976). 2008 Feb 15;33(4 Suppl):S39-51. doi: 10.1097/BRS.0b013e31816454c8.
Results Reference
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PubMed Identifier
18204388
Citation
Carragee EJ, Hurwitz EL, Cheng I, Carroll LJ, Nordin M, Guzman J, Peloso P, Holm LW, Cote P, Hogg-Johnson S, van der Velde G, Cassidy JD, Haldeman S; Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Treatment of neck pain: injections and surgical interventions: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Spine (Phila Pa 1976). 2008 Feb 15;33(4 Suppl):S153-69. doi: 10.1097/BRS.0b013e31816445ea.
Results Reference
background
PubMed Identifier
18204386
Citation
Hurwitz EL, Carragee EJ, van der Velde G, Carroll LJ, Nordin M, Guzman J, Peloso PM, Holm LW, Cote P, Hogg-Johnson S, Cassidy JD, Haldeman S; Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Treatment of neck pain: noninvasive interventions: results of the Bone and Joint Decade 2000-2010 Task Force on Neck Pain and Its Associated Disorders. Spine (Phila Pa 1976). 2008 Feb 15;33(4 Suppl):S123-52. doi: 10.1097/BRS.0b013e3181644b1d.
Results Reference
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Conservative Therapy Versus Epidural Steroids for Cervical Radiculopathy

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