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Clinical Trials/NCT03639454
NCT03639454CompletedNot Applicable

Effect on Symptomatic Release of Dry Needling on Patients With Biceps Tendinopathy

China Medical University Hospital1 site in 1 country30 target enrollmentStarted: September 18, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Visual Analog Scales

Study Overview

Brief Summary

Biceps tendinopathy is a common cause in shoulder-pain symptoms. The major mechanism is overuse of the biceps muscles. The long-term accumulated and poor repaired trauma causes myofascial trigger points in the related muscles.

We will conduct the randomized, single blind experiment to evaluate the immediate, short-term, and long-term effect of DN.

Detailed Description

Biceps tendinopathy is a common cause in shoulder-pain symptoms. The major mechanism is overuse of the biceps muscles. The long-term accumulated and poor repaired trauma causes myofascial trigger points in the related muscles. Common symptoms are pain in the anterior shoulders and radiating pain in the biceps. Pain can be further elicited with lifting, pulling and repetitive overhead activity. Therefore, it can have a major impact on the patient's activity of daily life.

The investigator performed dry needle (DN) treatments with acupuncture needles. Stimulating the effected muscle , the investigator move the needle forward and backward several times. Muscle twitch may occur by our procedure. The pain caused by myofascial trigger points can be decreased effective simultaneously. So far, there is no solid research or clinical trial to evaluate the efficacy of the treatment yet.

The investigator will conduct the randomized, single blind experiment to evaluate the immediate, short-term, and long-term effect of DN. Outcome measures include visual analog scale, shoulder pain and disability index, pressure pain threshold, pain-free grip test, muscle tone changes and ultrasonographic evaluation of biceps peritendinous effusion.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Subjects older than 20 years of age who can cooperate with the experimental volunteers.
  • •Suffering from biceps tendon lesions for more than one month, and subjective pain intensity (VAS) greater than 5 points.
  • •There is a local tender point in front of the shoulder, and the shoulder joint pronation test can induce pain.
  • •Under soft tissue ultrasound, the thickness of Biceps Peritendinous Effusion (BPE) on the affected side of the biceps tendon is greater than 1 mm.

Exclusion Criteria

  • •There are contraindications to general treatment, such as serious medical problems, recent serious trauma, or pregnant women.
  • •There has been a history of drug abuse (including excess alcohol) that affects pain assessors.
  • •Have received shoulder, neck or upper back surgery.
  • •People with central or peripheral nerve disease.
  • •Cognitive impairment, unable to cooperate with the experimenter.
  • •Patients currently receiving other treatments for Biceps tendinopathy

Arms & Interventions

Dry needling

Experimental

In this arm, the subjects will receive the intervention of DN on Day1, Day2 and Day4, in total 3 treatments and will be arrange to take efficacy two assessment on Day8 and Day15, separately.

Intervention: dry needling (Procedure)

Transcutaneous Electric Nerve Stimulation

Active Comparator

In this arm, the subjects will receive the intervention of Transcutaneous Electric Nerve Stimulation on Day1, Day2 and Day4, in total 3 treatments and will be arrange to take efficacy two assessment on Day8 and Day15, separately.

Intervention: Transcutaneous electrical nerve stimulation (Procedure)

Outcomes

Primary Outcomes

Visual Analog Scales

Time Frame: 1 day

The visual analogue scale or visual analog scale is a psychometric response scale which can be used in questionnaires. This tool used to help a person rate the intensity of certain sensations and feelings, such as pain. A straight line of 100mm is actually marked with 0 mm on the far left and 100mm on the far right. Two faces are drawn on both ends. Explain to the patient that 0 mm means no pain and 100 mm means very painful. From the left end The right shift indicates more and more pain. Take a pen and let the patient draw a short line vertically on the line, representing his painful position, and record the measured cm value. In this test, if the score of the subject decreases, it can represent the treatment is helpful for the improvement of the patient's pain.

Secondary Outcomes

  • Pressure Pain Threshold(1 day)
  • Muscle tension(1 day)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Li-Wei Chou

Minister of Rehabilitation

China Medical University Hospital

Study Sites (1)

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