- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05307211
Are Stabilization Exercises Effective After Epidural Steroid Injection in Patients With Cervical Radiculopathy?
May 17, 2023 updated by: Marmara University
Evaluation of the Effect of Stabilization Exercises on Interlaminar Epidural Steroid Injection Treatment Results in Cervical Radiculopathy
Cervical radiculopathy was first described in 1943 by researchers named Semmes and Murphy, years later than lumbosacral radiculopathy.
It is a neurological condition caused by dysfunction in the cervical spinal nerves, nerve roots, or both.
This compression occurs as a result of disc herniation, spondylosis, trauma, spinal tumors, etc.
As the first symptom, it manifests as pain.
When pain radiates from the neck to the shoulder and arm and is accompanied by sensory complaints and motor weakness, cervical radiculopathy should be suspected.
It is a significant cause of morbidity and disability in both men and women, and it occurs in middle age.
As a result, clinicians must quickly diagnose and determine the best treatment method.
The majority of the information in the literature on the incidence of cervical radiculopathy is based on the findings of a large population-based study conducted between 1976 and 1990 by the Mayo Clinic in Rochester, Minnesota.
The incidence rate of cervical radiculopathy was reported to be 83.2 per 100,000 per year in this study, which included 561 cases.
The primary goals of treatment are to alleviate pain, restore neurological function, and prevent a recurrence.
According to the literature, cervical radiculopathy recurs at a rate of 31.7%, and 26% of them go to surgery.
Treatment options vary depending on whether the symptoms are acute or chronic and their severity.
In the treatment of cervical radiculopathy, either conservative (non-operative) or surgical treatments are used.
In patients with chronic neck pain with or without radiculopathy, a cervical epidural steroid injection is one of the most frequently used interventional therapeutic options.
Chronic neck pain or radicular pain caused by disc herniation, spinal stenosis, or discogenic pain can also be treated with cervical epidural injections.
Cervical stability training is an exercise program that is used to strengthen the cervical spine, relieve pain, and improve functionality.
Changes in dynamic scapula stabilization are observed in patients with chronic neck pain.
The scapula connects the neck and shoulder, so it plays an important role in stabilizing the neck and shoulder complex.
Because of the interaction between the neck and the scapula, scapular stability becomes more important in these patients.
Study Overview
Status
Completed
Conditions
Detailed Description
Many studies in the literature separately investigate the effectiveness of Cervical Interlaminar Epidural Steroid Injection (CIESI) in radiculopathy due to cervical disc herniation or the effectiveness of stabilization exercises and physical therapy modalities in these patients.
However, there have been no studies on the effectiveness of post-injection exercise training as far as we are aware.
Our study aims to investigate the benefit of stabilization exercises after interlaminar epidural steroid injection in patients with radiculopathy caused by cervical disc herniation, add a new study to the literature, and guide future research.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Umut İslam Tayboğa, RA
- Phone Number: +905397173931
- Email: umutislamtayboga@outlook.com
Study Contact Backup
- Name: Osman Hakan Gündüz, MD
- Email: drhakang@gmail.com
Study Locations
-
-
Pendik
-
Istanbul, Pendik, Turkey, 34890
- Marmara University, Faculty of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Between the ages of 18-65
- Cervical radiculopathy has caused neck and arm pain for at least three months.
- Sign a consent form and volunteer to take part in the study.
Exclusion Criteria:
- Previous surgical/interventional procedure for the cervical region
- Presence of other musculoskeletal disorders (such as lateral epicondylitis, tendinitis, entrapment neuropathy) that may cause diagnostic confusion in terms of pain pattern and localization
- Signs of trauma, fracture, malignancy, or active infection
- Rheumatological (RA, AS, etc.), endocrinological (such as osteoporosis, Paget's disease), or another systemic disease that may change the anatomical or physiological structure of the relevant regions Presence of coagulopathy
- History of whiplash injury, cervical spinal stenosis, cervical spondylosis
- Being pregnant and breastfeeding
- Presence of mental deterioration or psychiatric/neurological disease that can affect the flow of the study.
- Having a history of allergic reactions to the injectables that will be used.
- Presence of cardiopulmonary disease that may lead to exercise intolerance (heart failure, chronic obstructive pulmonary disease, etc.)
- Failure to implement the exercise program regularly.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: GROUP 1 (CIESI Only)
Only interlaminar epidural steroid injection will be administered to patients in this arm with the same method as in the other arms (one session, week 0).
Staying active will be the only recommendation, and no exercise prescription will be provided.
|
Fluoroscopy-guided cervical interlaminar epidural steroid injection will be administered to patients with chronic neck pain due to cervical disc herniation.
The injection area is cleaned 3 times with an antiseptic solution and covered with a sterile cloth.
Local anesthesia with 2 ccs 3% prilocaine will be applied to the skin and subcutaneous tissues in the area of interest.
Under fluoroscopy guidance, the needle is advanced into the C7-T1 intervertebral disc level.
With the help of the loss of resistance technique, it is understood that the needle is in the epidural space, and second control is provided by administering contrast material.
After the confirmation of needle place is done, a mixture of 12 mg dexamethasone, 1 cc 2% lidocaine, 1 cc saline is injected.
The patient is taken to the restroom after the procedure and followed up for any complications.
|
Experimental: GROUP 2 (CIESI plus NECK STABILIZATION EXERCISES)
After the interlaminar epidural steroid injection, the patients will be taken to an exercise program in the physical therapy unit, in the company of a physiotherapist, within 24 hours, within 72 hours at the latest.
|
Fluoroscopy-guided cervical interlaminar epidural steroid injection will be administered to patients with chronic neck pain due to cervical disc herniation.
The injection area is cleaned 3 times with an antiseptic solution and covered with a sterile cloth.
Local anesthesia with 2 ccs 3% prilocaine will be applied to the skin and subcutaneous tissues in the area of interest.
Under fluoroscopy guidance, the needle is advanced into the C7-T1 intervertebral disc level.
With the help of the loss of resistance technique, it is understood that the needle is in the epidural space, and second control is provided by administering contrast material.
After the confirmation of needle place is done, a mixture of 12 mg dexamethasone, 1 cc 2% lidocaine, 1 cc saline is injected.
The patient is taken to the restroom after the procedure and followed up for any complications.
The physiotherapist will design an exercise protocol for neck stabilization.
Each exercise will be applied three days a week throughout a 4-week program, accompanied by a physiotherapist, and will begin with 7 to 10 repetitions at first, increasing to 10 to 15 repetitions in the following weeks, taking into account the patient's condition.
After the physiotherapist-assisted exercises are completed, the protocol will continue as home-based exercises until the assessments are completed.
|
Experimental: GROUP 3 ( CIESI plus NECK and SCAPULAR STABILIZATION EXERCISES)
After the interlaminar epidural steroid injection, the patients will be taken to an exercise program in the physical therapy unit, in the company of a physiotherapist, within 24 hours, within 72 hours at the latest.
|
Fluoroscopy-guided cervical interlaminar epidural steroid injection will be administered to patients with chronic neck pain due to cervical disc herniation.
The injection area is cleaned 3 times with an antiseptic solution and covered with a sterile cloth.
Local anesthesia with 2 ccs 3% prilocaine will be applied to the skin and subcutaneous tissues in the area of interest.
Under fluoroscopy guidance, the needle is advanced into the C7-T1 intervertebral disc level.
With the help of the loss of resistance technique, it is understood that the needle is in the epidural space, and second control is provided by administering contrast material.
After the confirmation of needle place is done, a mixture of 12 mg dexamethasone, 1 cc 2% lidocaine, 1 cc saline is injected.
The patient is taken to the restroom after the procedure and followed up for any complications.
The physiotherapist will design an exercise protocol for neck and scapular stabilization.
Each exercise will be applied three days a week throughout a 4-week program, accompanied by a physiotherapist, and will begin with 7 to 10 repetitions at first, increasing to 10 to 15 repetitions in the following weeks, taking into account the patient's condition.
After the physiotherapist-assisted exercises are completed, the protocol will continue as home-based exercises until the assessments are completed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of pain severity from baseline to each checkpoints
Time Frame: from pre-interventional time to post-interventional 1st hour, 1st month, 3rd month
|
The numerical rating scale (NRS) is widely used in research and clinical settings to represent pain intensity.
NRS is defined as 0 for the absence of pain and 10 as the worst possible pain.
The NRS is moderately reliable and has a clinically important difference (CID) value of 1.0.
|
from pre-interventional time to post-interventional 1st hour, 1st month, 3rd month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of functionality from baseline to each checkpoints
Time Frame: from pre-interventional time to post-interventional 1st month, 3rd month
|
The Neck Disability Index (NDI) is a validated 10-item questionnaire that measures a patient's self-reported disability due to neck pain.
The score ranges from 0 (no disability) to 100 (completely disabled).
The minimum detectable change (MDC) for patients with cervical radiculopathy is 10 points, and the clinically important difference (CID) is 14 points.
|
from pre-interventional time to post-interventional 1st month, 3rd month
|
Change of life quality from baseline to each checkpoints
Time Frame: from pre-interventional time to post-interventional 1st month, 3rd month
|
Short Form-12 (SF-12) is a scale that was developed in 1994 to evaluate the quality of life for the last four weeks without focusing on a specific age and disease group.
It consists of 12 questions, all selected from the SF-36 Health Questionnaire.
SF-12 consists of physical functionality, physical role, pain, general health, emotional role, mental health, social functionality, and vitality sub-components.
|
from pre-interventional time to post-interventional 1st month, 3rd month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Savaş Şencan, MD, Marmara University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 23, 2022
Primary Completion (Actual)
January 6, 2023
Study Completion (Actual)
April 29, 2023
Study Registration Dates
First Submitted
March 22, 2022
First Submitted That Met QC Criteria
March 23, 2022
First Posted (Actual)
April 1, 2022
Study Record Updates
Last Update Posted (Actual)
May 18, 2023
Last Update Submitted That Met QC Criteria
May 17, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 04.03.2022.357
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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