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Treatment for Ulnar Neuropathy at the Elbow (UNETREAT)

Primary Purpose

Peripheral Nervous System Diseases, Nerve Compression Syndromes, Cubital Tunnel Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
Slovenia
Study Type
Interventional
Intervention
Simple decompression of the ulnar nerve
Conservative treatment
Sponsored by
University Medical Centre Ljubljana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Nervous System Diseases focused on measuring Ulnar neuropathy at the elbow, Electromyography, Ultrasonography, Treatment, Surgery, Conservative treatment

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • continuous numbness or paresthesias in the 5th finger,
  • weakness of the ulnar-innervated muscles or hand clumsiness.

Exclusion Criteria:

  • previous elbow fracture or surgery,
  • polyneuropathy, symptoms of polyneuropathy, conditions causing polyneuropathy (e.g., diabetes) or multiple mononeuropathy,
  • motor neuron disorders (e.g., monomelic amyotrophy, amyotrophic lateral sclerosis - ALS).

Sites / Locations

  • University Medical Center Ljubljana, Department of Neurology, Institute of Clinical NeurophysiologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

UNE at HUA_HUA release

UNE at HUA_conservative treatment

UNE at RTC_HUA release

UNE at RTC_conservative treatment

Arm Description

Patients with UNE under the HUA randomly distributed for simple decompression of the ulnar nerve. Patients will also receive pictured recommendations with descriptions, which limb positions should be avoided. Control neurological examination will be performed every 3 months and identical protocol as at the time of diagnostic evaluation at 1 year follow-up.

Patients with UNE under the HUA randomly distributed for conservative treatment. Patients will receive pictured recommendations with descriptions, which limb positions should be avoided. In order to prevent deterioration in conservatively treated group of patients with UNE at HUA control neurological examination will be performed every 3 months. Criteria for surgical HUA release will be clinical deterioration or lack of clinical improvement after 12 months. Prior to surgical HUA release and at 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.

Patients with UNE in the RTC groove randomly distributed for simple decompression of the ulnar nerve. Patients will also receive pictured recommendations with descriptions, which limb positions should be avoided. At 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.

Patients with UNE in the RTC groove randomly distributed for conservative treatment. Patients will receive pictured recommendations with descriptions, which limb positions should be avoided. At 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.

Outcomes

Primary Outcome Measures

Improvement/remission
Primary outcome of the study will be percentage of patients with at least moderate symptoms improvement or complete remission

Secondary Outcome Measures

UNE symptoms
Percentage of patients without UNE symptoms or with minimal UNE symptoms

Full Information

First Posted
August 27, 2018
Last Updated
March 8, 2021
Sponsor
University Medical Centre Ljubljana
Collaborators
Slovenian Research Agency
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1. Study Identification

Unique Protocol Identification Number
NCT03651609
Brief Title
Treatment for Ulnar Neuropathy at the Elbow
Acronym
UNETREAT
Official Title
Treatment for Ulnar Neuropathy at the Elbow - a Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
September 1, 2022 (Anticipated)
Study Completion Date
September 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Centre Ljubljana
Collaborators
Slovenian Research Agency

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to investigate utility and appropriateness of treatment interventions taking into account the presumed mechanisms of two main varieties of ulnar neuropathy at the elbow (UNE). The investigators hypothesize that in patients with UNE under the humeroulnar aponeurosis (HUA) surgical HUA release (simple decompression) is superior to conservative treatment. By contrast, in patients with UNE at the retroepicondylar (RTC) groove surgical HUA release (simple decompression) should not be superior to conservative treatment.
Detailed Description
Ulnar neuropathy at the elbow (UNE) is the second most common focal neuropathy with annual incidence rate of 21 per 100.000. Therefore, in Slovenia UNE each year affects approximately 420 and in Europe 156.000 patients. In previous publications evidence was presented that idiopathic UNE consists of two conditions occurring 2-5 cm apart. In the first condition, affecting about 15% of UNE patients, the ulnar nerve is entrapped 2-3 cm distal to the medial epicondyle (ME) under the humeroulnar aponeurosis (HUA), i.e., in the cubital tunnel. In the second condition, affecting the majority (about 85%) of patients, the lesion is located at the ME or up to 4 cm proximally in the retroepicondylar (RTC) groove. As no anatomical structure constricting the ulnar nerve is usually found in that segment, the most probable cause of UNE at this location is extrinsic ulnar nerve compression against the underlying bone. The investigators believe that these two groups of UNE patients need different therapeutic approaches: (1) surgical release for ulnar nerve entrapment distal to ME and (2) conservative treatment for extrinsic nerve compression in the RTC groove. The efficiency of this therapeutic approach was already evaluated and significant clinical improvement was found in 80% of UNE patients. However, the design of that study did not enable to obtain an indisputable evidence that outcome was a result of treatment approach. It is still possible that improvement observed in patient population was a consequence of natural history rather than therapy. To resolve this problem a properly designed randomized control trial is needed. The investigators believe such trial would prevent numerous unnecessary and delayed operations in UNE patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Nervous System Diseases, Nerve Compression Syndromes, Cubital Tunnel Syndrome
Keywords
Ulnar neuropathy at the elbow, Electromyography, Ultrasonography, Treatment, Surgery, Conservative treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients with suspected UNE will be prospectively recruited in a single secondary referral center. First of three blinded examiners will obtain patients' history and perform focused neurological examination. The second examiner will perform electrodiagnostic (EDx) and the third ultrasonographic (US) studies. Patients with UNE under the HUA and in the RTC groove will be randomly distributed in two groups for surgical HUA release and conservative treatment. During surgical intervention the surgeon will cut the HUA with minimal incision technique. All patients (including surgically treated) will be given pictured recommendations with descriptions, which limb positions should be avoided. In order to prevent deterioration in conservatively treated group of patients with UNE at HUA, control neurological examination will be performed every 3 months. At 1 year follow-up we will use identical protocol as at the time of initial diagnostic evaluation.
Masking
Investigator
Masking Description
Three examiners will perform one part of diagnostic evaluation that will include: (1) patients' history and focused neurological examination, (2) (EDx) and (3) US studies. They will be blinded to the findings of the other parts of the evaluation.
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
UNE at HUA_HUA release
Arm Type
Experimental
Arm Description
Patients with UNE under the HUA randomly distributed for simple decompression of the ulnar nerve. Patients will also receive pictured recommendations with descriptions, which limb positions should be avoided. Control neurological examination will be performed every 3 months and identical protocol as at the time of diagnostic evaluation at 1 year follow-up.
Arm Title
UNE at HUA_conservative treatment
Arm Type
Active Comparator
Arm Description
Patients with UNE under the HUA randomly distributed for conservative treatment. Patients will receive pictured recommendations with descriptions, which limb positions should be avoided. In order to prevent deterioration in conservatively treated group of patients with UNE at HUA control neurological examination will be performed every 3 months. Criteria for surgical HUA release will be clinical deterioration or lack of clinical improvement after 12 months. Prior to surgical HUA release and at 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.
Arm Title
UNE at RTC_HUA release
Arm Type
Experimental
Arm Description
Patients with UNE in the RTC groove randomly distributed for simple decompression of the ulnar nerve. Patients will also receive pictured recommendations with descriptions, which limb positions should be avoided. At 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.
Arm Title
UNE at RTC_conservative treatment
Arm Type
Active Comparator
Arm Description
Patients with UNE in the RTC groove randomly distributed for conservative treatment. Patients will receive pictured recommendations with descriptions, which limb positions should be avoided. At 1 year follow-up identical protocol as at the time of diagnostic evaluation will be performed.
Intervention Type
Procedure
Intervention Name(s)
Simple decompression of the ulnar nerve
Intervention Description
Surgical HUA release 2-3 cm distal to medial epicondyle with minimal-incision technique .
Intervention Type
Behavioral
Intervention Name(s)
Conservative treatment
Intervention Description
Patients will be given pictured recommendations with descriptions, which limb positions should be avoided.
Primary Outcome Measure Information:
Title
Improvement/remission
Description
Primary outcome of the study will be percentage of patients with at least moderate symptoms improvement or complete remission
Time Frame
2 years
Secondary Outcome Measure Information:
Title
UNE symptoms
Description
Percentage of patients without UNE symptoms or with minimal UNE symptoms
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Muscle wasting_subjective
Description
Percentage of patients without hand muscle wasting
Time Frame
2 years
Title
Muscle wasting_objective
Description
Cross section area of the first dorsal interosseous (FDI) muscle measured by ultrasonography (US)
Time Frame
2 years
Title
Muscles strength_subjective
Description
Percentage of patients with near normal (4+/5 on MRC) or normal (5/5 on MRC) ulnar hand muscles strength
Time Frame
2 years
Title
Muscles strength_objective
Description
Improvement in strength of the first dorsal interosseous (FDI) muscle as measured by dynamometer (microFET2)
Time Frame
2 years
Title
Ulnar_CMAP_AMP
Description
Increase in amplitude (AMP) of the ulnar compound muscle action potential (CMAP)
Time Frame
2 years
Title
Ulnar_MNCV
Description
Increase of motor nerve conduction velocity (MNCV) in the most affected 2 cm segment
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: continuous numbness or paresthesias in the 5th finger, weakness of the ulnar-innervated muscles or hand clumsiness. Exclusion Criteria: previous elbow fracture or surgery, polyneuropathy, symptoms of polyneuropathy, conditions causing polyneuropathy (e.g., diabetes) or multiple mononeuropathy, motor neuron disorders (e.g., monomelic amyotrophy, amyotrophic lateral sclerosis - ALS).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gregor Omejec, PT, DSc
Phone
+386 1 522 1502
Email
gregor.omejec@kclj.si
First Name & Middle Initial & Last Name or Official Title & Degree
Simon Podnar, MD, DSc
Phone
+386 1 522 3076
Email
simon.podnar@kclj.si
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon Podnar, MD, DSc
Organizational Affiliation
Department of Neurology, University Medical Center Ljubljana
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Ljubljana, Department of Neurology, Institute of Clinical Neurophysiology
City
Ljubljana
ZIP/Postal Code
1000
Country
Slovenia
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No planning to share individual participant data.
Citations:
PubMed Identifier
25743266
Citation
Omejec G, Podnar S. Precise localization of ulnar neuropathy at the elbow. Clin Neurophysiol. 2015 Dec;126(12):2390-6. doi: 10.1016/j.clinph.2015.01.023. Epub 2015 Feb 14.
Results Reference
background
PubMed Identifier
26093933
Citation
Omejec G, Podnar S. What causes ulnar neuropathy at the elbow? Clin Neurophysiol. 2016 Jan;127(1):919-924. doi: 10.1016/j.clinph.2015.05.027. Epub 2015 Jun 17.
Results Reference
background
PubMed Identifier
29934265
Citation
Simon NG. Treatment of ulnar neuropathy at the elbow - An ongoing conundrum. Clin Neurophysiol. 2018 Aug;129(8):1716-1717. doi: 10.1016/j.clinph.2018.06.006. Epub 2018 Jun 18. No abstract available.
Results Reference
background
PubMed Identifier
29887400
Citation
Omejec G, Podnar S. Long-term outcomes in patients with ulnar neuropathy at the elbow treated according to the presumed aetiology. Clin Neurophysiol. 2018 Aug;129(8):1763-1769. doi: 10.1016/j.clinph.2018.04.753. Epub 2018 Jun 1.
Results Reference
background
PubMed Identifier
25541522
Citation
Omejec G, Zgur T, Podnar S. Diagnostic accuracy of ultrasonographic and nerve conduction studies in ulnar neuropathy at the elbow. Clin Neurophysiol. 2015 Sep;126(9):1797-804. doi: 10.1016/j.clinph.2014.12.001. Epub 2014 Dec 8.
Results Reference
background
PubMed Identifier
24985195
Citation
Omejec G, Podnar S. Normative values for short-segment nerve conduction studies and ultrasonography of the ulnar nerve at the elbow. Muscle Nerve. 2015 Mar;51(3):370-7. doi: 10.1002/mus.24328. Epub 2015 Jan 10.
Results Reference
background
PubMed Identifier
26971477
Citation
Omejec G, Podnar S. Proposal for electrodiagnostic evaluation of patients with suspected ulnar neuropathy at the elbow. Clin Neurophysiol. 2016 Apr;127(4):1961-7. doi: 10.1016/j.clinph.2016.01.011. Epub 2016 Jan 28.
Results Reference
background
PubMed Identifier
27552333
Citation
Omejec G, Zgur T, Podnar S. Can neurologic examination predict pathophysiology of ulnar neuropathy at the elbow? Clin Neurophysiol. 2016 Oct;127(10):3259-64. doi: 10.1016/j.clinph.2016.08.002. Epub 2016 Aug 9.
Results Reference
background
PubMed Identifier
27815973
Citation
Omejec G, Bozikov K, Podnar S. Validation of preoperative nerve conduction studies by intraoperative studies in patients with ulnar neuropathy at the elbow. Clin Neurophysiol. 2016 Dec;127(12):3499-3505. doi: 10.1016/j.clinph.2016.09.018. Epub 2016 Oct 13.
Results Reference
background
PubMed Identifier
29266317
Citation
Omejec G, Podnar S. Neurologic examination and instrument-based measurements in the evaluation of ulnar neuropathy at the elbow. Muscle Nerve. 2018 Jun;57(6):951-957. doi: 10.1002/mus.26046. Epub 2018 Jan 23.
Results Reference
background
PubMed Identifier
28345147
Citation
Podnar S, Omejec G, Bodor M. Nerve conduction velocity and cross-sectional area in ulnar neuropathy at the elbow. Muscle Nerve. 2017 Dec;56(6):E65-E72. doi: 10.1002/mus.25655. Epub 2017 Apr 15.
Results Reference
background
PubMed Identifier
27859367
Citation
Leis AA, Smith BE, Kosiorek HE, Omejec G, Podnar S. Complete dislocation of the ulnar nerve at the elbow: a protective effect against neuropathy? Muscle Nerve. 2017 Aug;56(2):242-246. doi: 10.1002/mus.25483. Epub 2017 Jan 4.
Results Reference
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Treatment for Ulnar Neuropathy at the Elbow

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