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Dry needling of shoulder pain

Comparison of the effect of the two different methods of dry needling in patients with shoulder impingement syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190409043210N1
Enrollment
66
Registered
2020-01-11
Start date
2020-02-04
Completion date
Unknown
Last updated
2020-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder impingement syndrome. Impingement syndrome of shoulder

Interventions

Intervention 1: First intervention group: Ten consecutive sessions of routine physical therapy for shoulder, including exercise and interferential therapy with hot pack and three sessions of deep dry

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: Impingement syndrome cases with positive Hawkins-kennedy and Neer’s sig presence of at least one active or inactive trigger point in the infraspinatus muscle matching Pattern of trigger points with patient pain based on references age between 20-55

Exclusion criteria

Exclusion criteria: Shoulder injection history shoulder surgery history glenohumeral instability Shoulder physiotherapy in the last 3 months Symptoms indicate systemic disorders Taking corticosteroid anti-inflammatory drugs over the past 3 months history of sport & over head activity Patients with any restrictions on dry needling

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before the intervention, at the end of tenth session, and four weeks after the last session of treatment. Method of measurement: Numeric pain rating scale.;Shoulder pain and disability. Timepoint: Before the intervention, at the end of tenth session, and four weeks after the last session of treatment. Method of measurement: Shoulder Pain and Disability Index.;Pressure pain threshold. Timepoint: Before the intervention, at the end of tenth session, and four weeks after the last session of treatment. Method of measurement: Digital pain pressure algometer (Wagner RS232).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Emani

Shiraz University of Medical Sciences

m_emani@sums.ac.ir+98 71 3627 1551

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026