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Mechanical Neck PainNCT07027631

Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal Shockwave Therapy on Chronic Mechanical Neck Pain

A study testing Magnesium Sulfate Iontophoresis, Shock Wave Therapy and stretching and strengthening in people with Mechanical Neck Pain, run by Beni-Suef University at 1 site in Egypt.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

The purpose of the study is to investigate the Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal shockwave therapy on Chronic Mechanical Neck Pain Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Mechanical Neck Pain
What is being tested?
Magnesium Sulfate Iontophoresis, Shock Wave Therapy and stretching and strengthening
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteEgypt
Study dates
20 Jun 2025to 1 Oct 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

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 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • medically competent men and women will be included
  • They had chronic MTrPs in the upper trapezius for more than 6 months
  • Diagnostic criteria of being a tight band with a palpable nodule and distant pain when subjected to pressure

Who cannot join

  • subjects with previous neck or shoulder pathology (e.g., fracture, sur¬gery, inflammatory and infectious diseases),
  • cervical disc pathology, systemic disorder, fibromyalgia,
  • those who underwent physical therapy for at least the previous 3 months

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Egypt1 site
  • Faculty of Physical Therapy

    Giza

Other trials in Egypt

About this study

Official title: Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal Shockwave Therapy on Chronic Mechanical Neck Pain. A Randomized Controlled Trial

The purpose of the study is to investigate the Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal shockwave therapy on Chronic Mechanical Neck Pain

Being tested
Magnesium Sulfate Iontophoresis, Shock Wave Therapy, stretching and strengthening
Keywords
shock wave therapy, Magnesium Sulfate iontophoresis, low back pain
Medical subject headings
Low Back Pain

What participants receive

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

  • Magnesium Sulfate IontophoresisDevice

    Magnesium Sulfate iontophoresis utilizing an iontophoretic drug delivery system

  • Shock Wave TherapyDevice

    using Shock Wave Therapy Device

  • stretching and strengtheningOther

    stretching and strengthening exercises

Study groups in NCT07027631
Study groupRoleWhat they receive
Magnesium Sulfate Iontophoresis groupExperimentalPatients in this group will receive Magnesium Sulfate Iontophoresis, two sessions per week for four weeks
Receives: Device: Magnesium Sulfate Iontophoresis
Shock Wave Therapy groupExperimentalPatients in this group will receive Shock Wave Therapy, one session per week for four weeks
Receives: Device: Shock Wave Therapy
Control groupPlacebo comparatorPatients in this group will receive stretching and strengthening exercises, two sessions per week for four weeks
Receives: Other: stretching and strengthening

What is being measured

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

  1. pain pressure threshold

    pain pressure threshold will be measured by the pressure algometer

    Measured: 0-4 weeks

  2. Pain intensity

    pain intensity will be measured by visual analogue scale

    Measured: 0-4 weeks

Secondary outcomes (1)
  1. Neck Disability Index

    Neck Disability Index is a questionnaire to measure function

    Measured: 0-4 Weeks

Timeline

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

  1. First posted18 Jun 2025
  2. Study start20 Jun 2025
  3. Primary completion20 Sep 2025 (estimated)
  4. Study completion1 Oct 2025 (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
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07027631
Sponsor's protocol ID
BeniSuefU24
Status last verified
Aug 2025
First submitted
11 Jun 2025
Last updated
7 Aug 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Magnesium Sulfate Iontophoresis, Shock Wave Therapy and stretching and strengthening in people with Mechanical Neck Pain, run by Beni-Suef University at 1 site in Egypt.

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 3 inclusion and 3 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: enrolling by invitation, as of the sponsor's last update on 7 Aug 2025. 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 Egypt. 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. Some participants in this study may receive a placebo. 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?

This study is still under way. Results are not available in the source record yet.

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?

pain pressure threshold (time frame: 0-4 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 7 Aug 2025.

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