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Completed

NCT Number: NCT06573775

Evaluation of Pain Quality in Young Swimmers Suffering From Myofascial Pain Syndrome Using Lidocaine Phonophoresis

To evaluate pain quality by pain quality assessment scale (PQAS) using lidocaine phonophoresis on myofascial pain syndrome (MPS) in athletic children.

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Key information

Age range

10 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

College of Medicine

Ismailia, 41522, Egypt

About this study

Forty five males athletic swimmer children (10 to 14 years old) with MPS in the upper trapezius muscle were evaluated before and after treatment. They were randomly divided into three groups, n=15 children each. A (control), B and C (study groups). The three groups received spatial designed physical therapy program. The two study groups received pulsed ultrasound and lidocaine phonophoresis repectively. The duration of treatment was 40 minutes, three times / weeks for three successive months.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age range from 10 to 14 years.
  • All children have regional neck pain complaint.
  • Tenderness in cervical trigger points in the midpoint of the upper border of trapezius muscle, from grade II to grade IV according to tenderness grading scheme (Hubbard and Berkoff, 1993) (Appendix I )
  • The diagnosis of an active MTrP in the upper trapezius according to (Ardiçet al . , 2002 and Bruno, 2005):
  • Patients suffered from active MTrPs in the upper trapezius.
  • Tender spots in one or more palpable taut bands.
  • A typical pattern of referred pain distributed in the ipsilateral, posterolateral cervical paraspinal area, mastoid process or temporal area
  • Palpable or visible local twitch response on snapping palpation at the most sensitive spot in the taut band.
  • Restricted range of motion in lateral bending of the cervical spine to the opposite side.
  • Palpation of a trigger point elicits a stereotypic zone of referred pain specific to that muscle.
  • Identification of a palpable taut band, as well as a palpable, and exquisitely tender spot along the length of that taut band.
  • All children allowed to practice their regular sport activities.

Exclusion criteria

  • Neurological disorders.
  • Dermatological disorders.
  • Acute trauma prior to the study.
  • Fibromyalgia, systemic disease and drug allergy history were excluded from the study.
  • Having myofascial trigger points injection.
  • Chronic pain in both sides of the body.
  • History of findings of cervical injury whether orthopedic or soft tissue injury

Treatment and study plan

pulsed ultrasound

Device

treatment of myofacial trigger points with therapeutic ultrasound

Myofascial Release

Other

manual massage and range of motion exercises

Other names: myofascial trigger point realease

lidocaine phonophoresis

Device

transdermal tranmission of lidocaine molecules via ultrasound

Primary outcomes

  1. pain quality

    Time frame: 6 weeks

    pain quality assessment scale with zero indication of better outcome and twenty means the worst outcome

Secondary outcomes

  1. serum cortisol level

    Time frame: 6 weeks

    measurement of serum cortisol level

Sponsors and collaborators

Lead sponsor

New Ismailia National University

Other

Registry information

Official study title

Evaluation of Pain Quality in Young Swimmers Suffering From Myofascial Pain Syndrome Using Lidocaine Phonophoresis: A Randomized Controlled Trial

Acronym: MPS

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Aug 27, 2024
Registry last updated
Aug 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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