Percutaneous Electrical Nerve Stimulation Compared to Passive Assisted Neurodynamics in Brachial Plexus Neuropathy
Primary Purpose
Percutaneous Electrical Nerve Stimulation, Peripheral Neuropathy, Neuropathic Pain
Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Percutaneous Electrical Nerve Stimulation
Neurodynamic and manual therapy
Sponsored by
About this trial
This is an interventional treatment trial for Percutaneous Electrical Nerve Stimulation
Eligibility Criteria
Inclusion Criteria:
- Subjects with upper limb neural symptomatology between 18 and 60 years of age, presenting two or more of the following conditions:
- Paresthesias in any territory of the shoulder girdle, arm or hand
- Pain at rest in any territory of the upper extremity.
- Pain at rest in any upper extremity territory
- Sensations of electric shock in any territory of the shoulder girdle, arm or hand.
- Allodynia or cutaneous hyperalgesia in any territory of the shoulder girdle, arm or hand.
Exclusion Criteria:
- Less than 2 weeks of evolution
- Fracture in the affected upper extremity
- Suffering from another joint disorder such as osteoarthritis or rheumatic disease
- Suffering from generalized neuropathies due to neuromuscular disease or medication
- Inability to understand instructions or sign informed consent.
- Wearing a pacemaker or any electrical device implanted in the body
- Epilepsy
- Aversion or fear of needles
- Pregnant.
Sites / Locations
- Physiotherapy and exercise center OrigenkinesisRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
PENS
Neurodynamics and manual therapy
Arm Description
Outcomes
Primary Outcome Measures
Lanss Scale
Useful to identify patients with a pain experience dominated by neuropathic mechanisms. It is based on the analysis of sensory description and exploration of sensory dysfunction at the patient's bedside. It consists of 7 items and is scored from 0 to 24. At a score of less than 12, the neuropathic component is considered unlikely. A score greater than or equal to 12 is considered probable neuropathic pain. It is a validated scale for patients with neuropathic pain.
Pain Detect Scale
Screening questionnaire for neuropathic pain. This scale consists of a section dedicated to pain intensity and another that is responsible for assessing the qualitative aspect of pain, i.e., identifying whether the pain is of neuropathic characteristics. In the total of this scale the maximum possible score is 38 points and the minimum -1. For screening purposes, a score less than or equal to 12 is considered an unlikely neuropathic component. A score greater than or equal to 19 concludes that the neurological component in pain is probable.
Numerical Pain Rating Scale (NPRS)
A unique 11-point numerical scale validated in patients with various painful conditions. Data obtained through NPRS are easily documented, intuitively interpretable, and meet regulatory requirements for pain assessment and documentation. This scale is reliable and validated for assessing patients with pain20. Score 0 corresponds to "no pain" and score 10 corresponds to "maximum possible pain". In this study, patients were asked to mark their maximum pain detected in the last week (NPRS Max) and their minimum pain detected in the last week (NPRS Min).
Secondary Outcome Measures
Neural stress test
Nerves react to certain mechanical stresses and forces, but to establish positivity of such tests, the possibilities of "false positivity" due to other non-nerve structures must first be eliminated. The determination of a positive neural test is established by provocation and symptom relief techniques. In this outcome measure only a positive or negative test was considered. The test was positive if the patient's neural symptoms were reproduced during provocation, or negative if no such symptoms occurred.
DASH scale
It is a validated scale for assessing upper limb functionality. It is an instrument that can be completed by the patient with the help of the physical therapist. It consists of 30 questions that assess certain symptoms, as well as the ability to perform activities, ranging from 1 to 5, with 1=no difficulty and 5=maximum difficulty. The higher the score, the greater the upper limb disability.
Thermography
A thermal camera, HT-02D infrared thermographic and visible light camera with IR 1024 pixels and -20~300°C, 6Hz refresh rate, infrared thermometer was used. The thermograph indicates the approximate temperature of the body segment to be examined by focusing it with the thermographic camera.
Full Information
NCT ID
NCT05432973
First Posted
June 21, 2022
Last Updated
June 21, 2022
Sponsor
Universidad Rey Juan Carlos
1. Study Identification
Unique Protocol Identification Number
NCT05432973
Brief Title
Percutaneous Electrical Nerve Stimulation Compared to Passive Assisted Neurodynamics in Brachial Plexus Neuropathy
Official Title
Efficacy of Percutaneous Electrical Nerve Stimulation Compared With Passive Assisted Neurodynamics in Brachial Plexus Neuropathy: a Pilot Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2022 (Actual)
Primary Completion Date
December 1, 2022 (Anticipated)
Study Completion Date
January 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad Rey Juan Carlos
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Brachial plexus neuropathies, specifically of the median, radial, ulnar, suprascapular, axillary and dorsal scapular nerves, can arise when a peripheral nerve trunk or nerve root is subjected to injury, compression, inflammation or ischemia, resulting in reduced physical capabilities of the peripheral nervous system. Although pharmacological treatments provide mild symptomatic relief in the short term, they are not without side effects.
Neurostimulation techniques may be an effective treatment option for peripheral brachial plexus neuropathies. Some of these procedures are transcutaneous electrical nerve stimulation (TENS) or percutaneous electrical nerve stimulation (PENS). Although some case series have documented a positive effect in relation to ultrasound-guided PENS for subjects with subacromial pain syndrome or postsurgical pain, the lack of studies, to our knowledge, analyzing the effects of percutaneous electrical nerve stimulation, in relation to pain and paresthesias in subjects with brachial plexus neuropathy, warrants investigation for this goal.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Percutaneous Electrical Nerve Stimulation, Peripheral Neuropathy, Neuropathic Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
11 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
PENS
Arm Type
Experimental
Arm Title
Neurodynamics and manual therapy
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Percutaneous Electrical Nerve Stimulation
Intervention Description
In the PENS treatment, a biphasic continuous waveform current with a frequency of 2 Hz, a pulse width of 50 microseconds and an intensity that produces visible motor responses of the innervated muscles was used, below the patient's pain threshold. The NT6021 Percutaneous Neuromodulation equipment of the Nutek® brand distributed by Fisiolab Ibérica® was used. This equipment has the CE marking, which denotes compliance with the requirements of the legislation of Royal Decree 414/1996 of March 1, which regulates medical devices. B.O.E. of April 24, 1996
Intervention Type
Procedure
Intervention Name(s)
Neurodynamic and manual therapy
Intervention Description
The manual therapy consisted of passive-assisted mobilization and massage therapy of the muscular and fascial tissue, beginning with the cervical area, kneading while asking the patient to rotate the neck and then in the same way along the muscles and soft tissues innervated by the target nerve.
Neurodynamic was performed in a passive-assisted manner, combining the patient's cervical mobilizations with the mobility of the upper limbs adapted to each case.
Primary Outcome Measure Information:
Title
Lanss Scale
Description
Useful to identify patients with a pain experience dominated by neuropathic mechanisms. It is based on the analysis of sensory description and exploration of sensory dysfunction at the patient's bedside. It consists of 7 items and is scored from 0 to 24. At a score of less than 12, the neuropathic component is considered unlikely. A score greater than or equal to 12 is considered probable neuropathic pain. It is a validated scale for patients with neuropathic pain.
Time Frame
10 minutes
Title
Pain Detect Scale
Description
Screening questionnaire for neuropathic pain. This scale consists of a section dedicated to pain intensity and another that is responsible for assessing the qualitative aspect of pain, i.e., identifying whether the pain is of neuropathic characteristics. In the total of this scale the maximum possible score is 38 points and the minimum -1. For screening purposes, a score less than or equal to 12 is considered an unlikely neuropathic component. A score greater than or equal to 19 concludes that the neurological component in pain is probable.
Time Frame
10 minutes
Title
Numerical Pain Rating Scale (NPRS)
Description
A unique 11-point numerical scale validated in patients with various painful conditions. Data obtained through NPRS are easily documented, intuitively interpretable, and meet regulatory requirements for pain assessment and documentation. This scale is reliable and validated for assessing patients with pain20. Score 0 corresponds to "no pain" and score 10 corresponds to "maximum possible pain". In this study, patients were asked to mark their maximum pain detected in the last week (NPRS Max) and their minimum pain detected in the last week (NPRS Min).
Time Frame
1 minute
Secondary Outcome Measure Information:
Title
Neural stress test
Description
Nerves react to certain mechanical stresses and forces, but to establish positivity of such tests, the possibilities of "false positivity" due to other non-nerve structures must first be eliminated. The determination of a positive neural test is established by provocation and symptom relief techniques. In this outcome measure only a positive or negative test was considered. The test was positive if the patient's neural symptoms were reproduced during provocation, or negative if no such symptoms occurred.
Time Frame
5 minutes
Title
DASH scale
Description
It is a validated scale for assessing upper limb functionality. It is an instrument that can be completed by the patient with the help of the physical therapist. It consists of 30 questions that assess certain symptoms, as well as the ability to perform activities, ranging from 1 to 5, with 1=no difficulty and 5=maximum difficulty. The higher the score, the greater the upper limb disability.
Time Frame
5 minutes
Title
Thermography
Description
A thermal camera, HT-02D infrared thermographic and visible light camera with IR 1024 pixels and -20~300°C, 6Hz refresh rate, infrared thermometer was used. The thermograph indicates the approximate temperature of the body segment to be examined by focusing it with the thermographic camera.
Time Frame
10 minutes
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects with upper limb neural symptomatology between 18 and 60 years of age, presenting two or more of the following conditions:
Paresthesias in any territory of the shoulder girdle, arm or hand
Pain at rest in any territory of the upper extremity.
Pain at rest in any upper extremity territory
Sensations of electric shock in any territory of the shoulder girdle, arm or hand.
Allodynia or cutaneous hyperalgesia in any territory of the shoulder girdle, arm or hand.
Exclusion Criteria:
Less than 2 weeks of evolution
Fracture in the affected upper extremity
Suffering from another joint disorder such as osteoarthritis or rheumatic disease
Suffering from generalized neuropathies due to neuromuscular disease or medication
Inability to understand instructions or sign informed consent.
Wearing a pacemaker or any electrical device implanted in the body
Epilepsy
Aversion or fear of needles
Pregnant.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Víctor Navarro López, PhD student
Phone
697371075
Email
victor.navarro@urjc.es
Facility Information:
Facility Name
Physiotherapy and exercise center Origenkinesis
City
Alcorcón
State/Province
Madrid
ZIP/Postal Code
28922
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Víctor Navarro López, PhD student
Phone
697371075
Email
victor.navarro@urjc.es
12. IPD Sharing Statement
Plan to Share IPD
Yes
Learn more about this trial
Percutaneous Electrical Nerve Stimulation Compared to Passive Assisted Neurodynamics in Brachial Plexus Neuropathy
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