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A Randomized Controlled Trial for Articular Cavity Injection Combined with Osteopathic Manipulation on Frozen Shoulder in Early and Middle Stages

Clinical Effect of Articular Cavity Injection Combined with Osteopathic Manipulation on Frozen Shoulder in Early and Middle Stages

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034174
Enrollment
Unknown
Registered
2020-06-27
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

Frozen shoulder

Interventions

Experimental group:Articular cavity injection combined with osteopathic manipulation
control group:Oral meloxicam tablets, external warm meridian stick plaster, meridian stick gel

Sponsors

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Pain of shoulder joint with limited movement for more than 4 weeks; 2. Patients with severe shoulder pain, affecting daily life or work; 3. Patients with nocturnal pain; 4. The movement of painful shoulder joint is limited, active and passive lifting or external rotation is limited; 5. There is no obvious abnormality in the imaging examination, and osteoporosis may occur in the elderly; 6. No secondary factors. Inclusion criteria: 1. patients with the above diagnostic criteria, aged >=50 years old; 2. The frequency of joint pain in the last month was more than 1 / 2 for patients with a duration of at least 1 month and less than 1 year; 3. The degree of pain should meet the VAS score >=5.0; 4. Patients who did not receive glucocorticoid injection in the past three months; 5. Patients who did not receive sodium hyaluronate injection in the past year; 6. The observation group received invasive treatment.

Exclusion criteria

Exclusion criteria: 1. Musculoskeletal system: In the past three months, there were clear pain caused by trauma or sports injury; Mechanical or pathological fracture; Shoulder pain caused by cervical spondylosis; In the past half a year, shoulder implant operation; Infectious, rheumatic, rheumatoid, ankylosing spondylitis and reactive arthritis; Shoulder pain caused by gout and abnormal metabolism of calcium and phosphorus; Severe joint swelling; Tendon rupture of supraspinatus or infraspinatus after trauma; Simple fasciitis or soft tissue strain; Polymyositis, dermatomyositis and other immune system diseases; 2. General status: Mental disorders such as severe anxiety or depression; Serious cardiovascular and cerebrovascular diseases; Recent cardiovascular and cerebrovascular events in the past six months; The function of liver and kidney was abnormal; Allergic constitution; Malignant tumor, bleeding disease, etc.

Design outcomes

Primary

MeasureTime frame
VAS;SPADI;

Secondary

MeasureTime frame
Fugl-Meyer shoulder range of motion scale;Constant-Murley Shoulder Function Assessment Form Score;

Countries

China

Contacts

Public ContactHan Qingmin

The Third Affiliated Hospital of Guangzhou University of Chinese Medicine

hqm@gzhtcm.edu.cn+86 13380011307

Outcome results

None listed

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