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OpenTrials
Completed

NCT Number: NCT06610032

The Effect of Mesotherapy and Intra-articular Steroid Injection in Shoulder Pain

Patients with chronic shoulder pain will be divided randomly into mesotherapy and intra-articular steroid injection groups. Pain severity, range of motion and functional impairment will evaluated before treatment, 30 minutes and 4 weeks after the injections.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Health Science University Haydarpasa Numune Research and Training Hospital

Istanbul, Üsküdar, 34668, Turkey (Türkiye)

About this study

The study will include 84 patients aged 18-75 who applied to physical medicine and rehabilitation out-patient clinic with chronic shoulder pain between May and July 2024. Patients will be randomly divided into two groups: a mesotherapy group and steroid injection group, using the closed-envelope method. In the first group, a total of 3 sessions of mesotherapy are applied to the shoulder areas of the patients, 7 days apart. A single-session intra-articular 20 mg triamcinolone hexacetonide injection will be administered for patients in group 2. Pain severity, range of motion and functional impairment will evaluated before treatment, 30 minutes and 4 weeks after the injections.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Ages 18-75
  • Having shoulder pain for 6 months
  • VAS (Visual Analog Scale) > 4
  • Patients who can receive verbal instructions and do not have cognitive deficits

Exclusion criteria

  • Physical therapy applied to the shoulder area in the last 3 months
  • Having had a shoulder joint injection in the last 3 months
  • History of previous upper extremity surgery
  • History of drug allergy
  • Use of anticoagulant drugs (warfarin, low molecular weight heparin), patients with coagulation disorder
  • History of malignancy
  • Psychiatric illness
  • A rheumatological diagnosis such as Polymyalgia Rheumatica, Rheumatoid Arthritis, Ankylosing Spondylitis
  • Kidney failure
  • Liver disease
  • Heart failure
  • Pregnancy
  • Presence of infection, wound, allergy, burn-like lesions in the application area

Treatment and study plan

Mesotherapy

Procedure

A total of 3 sessions of mesotherapy will be applied to the shoulder area of the patients, 7 days apart in group 1.

Other names: Intra-articular steroid injection

Intra-articular steroid injection

Procedure

Single session intra-articular 20 mg triamcinolone hexacetonide injection will be applied for patients in group 2.

Other names: Mesotherapy

Primary outcomes

  1. VAS (Visual Analouge Scale)

    Time frame: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.

    Pain Severity evaluation ((0 (no pain)-10 (unbearable pain))

  2. Shoulder Disability Questionnaire' (OSS) form

    Time frame: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.

    Functional Disability evaluation (0-100)

  3. Goniometric shoulder range of motion

    Time frame: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.

    shoulder range of motion evaluation

Sponsors and collaborators

Lead sponsor

Haydarpasa Numune Training and Research Hospital

Other

Registry information

Official study title

The Comparison o the Efficacy of Mesotherapy and Intra-articular Steroid Injection in Patients With Chronic Shoulder Pain

Acronym: Mesotherapy

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 24, 2024
Registry last updated
Dec 18, 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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