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Carpal Tunnel SyndromeNCT05681663

The Effectiveness of Extracorporeal Shock Wave Therapy for Management of Carpal Tunnel Syndrome

A study testing Electroshock Wave therapy in people with Carpal Tunnel Syndrome, run by Ahi Evran University Education and Research Hospital at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Peripheral nerve entrapment neuropathies are the most common mononeuropathies in clinical practice. Carpal Tunnel Syndrome (CTS), n. It occurs as a result of compression of the medianus as it passes through the carpal tunnel, a narrow osteofibrous canal. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Carpal Tunnel Syndrome
What is being tested?
Electroshock Wave therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Feb 2023to 1 May 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Those diagnosed with Carpal Tunnel Syndrome

Who cannot join

  • Those with systemic disease

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Kırşehir ahi Evran Üniversitesi

    Kırşehir, Central Anatolia

Other trials in Turkey (Türkiye)

About this study

Official title: The Effectiveness of Different Pressure of Extracorporeal Shock Wave Therapy for Management of Carpal Tunnel Syndrome: a Randomized Controlled Trial

Peripheral nerve entrapment neuropathies are the most common mononeuropathies in clinical practice. Carpal Tunnel Syndrome (CTS), n. It occurs as a result of compression of the medianus as it passes through the carpal tunnel, a narrow osteofibrous canal. CTS is the most common entrapment neuropathy of the upper extremity, affecting approximately 3% of the general adult population.

This study, which was designed as a randomized controlled study, will include 36 patients with CTS, aged between 18-65, who applied to Kırşehir Ahi Evran University Training and Research Hospital. In our study, both groups will be given 10 minutes of paraffin, 20 minutes of TENS, and 10 repetitions of tendon gliding exercise, 3 days a week for a total of 3 weeks (9 sessions). EESDT will be applied once a week in both groups (one group at 4 bar and the other at 1.5 bar pressure). Measurements will be made before treatment, after treatment, and at 12 weeks post-treatment.

In the literature, different pressure parameters were used in studies examining the efficacy of ESDT in the treatment of CTS. Although ESDT has been shown to have a curative effect on CTS, there is no consensus on which pressure parameter is more effective. Therefore, in this study, the effectiveness of ESDT applied at different pressure parameters in the treatment of CTS will be examined.

Read the detailed description

Compression of peripheral nerves in fibroosseous tunnels located at segmental passages in the body is called entrapment neuropathy. In this type of neuropathies, the peripheral nerve is exposed to a neuropraxia-type injury in the area where it is compressed (1, 2). As a result, a picture develops in the distal part of the injured area, which leads to long-term motor, sensory and autonomic pathologies, and reduces the quality of life and functionality (3).

Carpal Tunnel Syndrome (CTS) occurs when the median nerve is exposed to compression during its passage through the carpal tunnel (4). Although CTS is the most common impingement neuropathy in the upper extremity, it has been reported to affect approximately 3% of the adult population (5). Although the incidence of CTS in women is three times higher than in men, the prevalence and severity increase with age. Work-related activities that require high-frequency repetition and force or the use of hand-operated vibrating tools significantly increase the risk of CTS (6).

CTS symptoms are generally characterized by pain and paresthesia in the innervation area of the median nerve in the hand region. Although these symptoms vary, they can sometimes be seen in the entire hand, rarely in the forearm and shoulder region. Repetitive wrist movements such as driving a vehicle, doing repetitive work with hand tools, squeezing diapers, and opening jars are activities that provoke the existing pathology. Patients generally report that their complaints decrease when they hold their hands down and shake them. This condition is known clinically as the Flick Sign and is 93% sensitive and 96% specific for CTS (7). As the anatomical localization within the carpal tunnel, the sensory fibers are subjected to compression before compared to the motor fibers, and only pain and paresthesia are seen in acute CTS. In severe cases where motor fibers are also affected, muscle weakness characterized by thumb abduction and oposition weakness is added to the present picture (8).

There are two different treatment options in CTS, conservative and surgical. In the conservative treatment of CTS; Conservative treatment methods such as local steroid injection, nonsteroidal anti-inflammatory drugs, diuretics, pyridoxine, splint, daily living activities, tendon-nerve slide exercises, manipulation, physical therapy, acupuncture, vitamin B6 are used. The approach in surgical treatment is surgical decompression and it is performed to relax the median nerve by loosening the transverse carpal ligament (9).

Eisenmenger defined the physical properties of extracorporeal shock wave therapy (ESDT) for the first time in 1959 and stated that high-intensity sound waves are applied to the body in the EIST treatment method (10). Shock waves were first applied to break up kidney stones in the 1980s. As the changes in the ilium were noticed while breaking the lower ureteral stones, studies were also started on bone tissues. Since 1990, research has been carried out on the use of this method in orthopedic diseases (11). ESDT has recently been widely used by orthopedists in Europe and the interest in its application has increased, and thousands of patients are treated with this method in the world (12).

Shock waves are caused by sudden changes in pressure, and these changes in pressure create strong waves that cause tension and compression. Shock wave is defined as acoustic wave. In sinusoidal shock waves, the pressure rises rapidly with a positive pressure (100-1000 bar) in as little as a few nanoseconds (ns) (less than 1 microsecond), followed by a rapid decrease and negative pressure.

The phase time of the wave is very short, the phase duration is defined in an average of 10 milliseconds (ms). Its frequency ranges from 16 hertz (Hz) to 20 megahertz (MHz). In this way, the energy is broken and reflected as it passes through areas such as bone and soft tissue, and the resulting kinetic energy affects the tissues. With the energy of the shock wave, cavitation occurs in the tissue and a force such as pressure and fragmentation occurs. Absorption of shock waves into the tissue is provided by conductive gels (11, 13).

In one study, a systematic review and analysis of randomized controlled trials was conducted on the effect of ESDT on CTS. In this study, 6 randomized controlled trials were examined. In conclusion, this meta-analysis revealed that ESDT can improve symptoms, functional outcomes and electrophysiological parameters in patients with CTS (10). In the literature, different pressure parameters have been used in studies examining the effectiveness of ESDT in the treatment of CTS (14,15,16). Although ESDT has been shown to have a curative effect on CTS (17), there is no consensus on which pressure parameter is more effective. Therefore, in this study, the effectiveness of ESDT applied at different pressure parameters in the treatment of CTS will be examined.

Being tested
Electroshock Wave therapy
Medical subject headings
Carpal Tunnel Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Electroshock Wave therapyOther

    Also called Parafin, Hotpack, Exercises, Splinting

    Randomized- Controlled trial

Study groups in NCT05681663
Study groupRoleWhat they receive
1.5 bar groupExperimental1. TENS, Parafin, exercise and In addition, 5 hertz 2000 pulses 1.5 bar ESWT will be applied to this group.
Receives: Other: Electroshock Wave therapy
4 bar groupExperimental1. TENS, Parafin, exercise and In addition, 5 hertz 2000 pulses 4 bar ESWT will be applied to this group.
Receives: Other: Electroshock Wave therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual Analogue Scale (VAS)

    A Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.

    Measured: 6 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Jan 2023
  2. Study start1 Feb 2023 (estimated)
  3. Primary completion1 Mar 2023 (estimated)
  4. Study completion1 May 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Masking
Single blind
Who is masked
Investigator
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05681663
Sponsor's protocol ID
43834581758
Status last verified
Jan 2023
First submitted
29 Dec 2022
Last updated
12 Jan 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Ceylan I, Kurtuncuoglu B, Tuncay F, Canli M, Alkan H, Tayfur A. Comparison of high- and low-dose radial extracorporeal shock wave therapy in carpal tunnel syndrome. Rev Assoc Med Bras (1992). 2025 May 2;71(3):e20241815. doi: 10.1590/1806-9282.20241815. eCollection 2025.

    PubMed 40332277

Questions about this trial

What is this clinical trial studying?

A study testing Electroshock Wave therapy in people with Carpal Tunnel Syndrome, run by Ahi Evran University Education and Research Hospital at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 12 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analogue Scale (VAS) (time frame: 6 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05681663, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Jan 2023.

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