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A randomized controlled trial for Shi's shoulder joint manipulation lysis in the treatment of frozen shoulder

A randomized controlled trial for Shi's shoulder joint manipulation lysis in the treatment of frozen shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036666
Enrollment
Unknown
Registered
2020-08-24
Start date
2021-01-01
Completion date
Unknown
Last updated
2020-09-21

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:Shi's shoulder joint manipulation release
The control group:Intraarticular injection of the shoulder joint

Sponsors

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 40-70 years; 2. Meet the diagnostic criteria of frozen shoulder, shoulder joint activity was significantly limited; 3. To be able to understand the accidents and risks that may occur in the process of release of Shi's manipulation after anesthesia and anesthesia; 4. Before treatment, shoulder orthostatic X-ray or shoulder MRI were taken to exclude other injuries around the shoulder; 5. Patients who have been in the clinic for more than 3 months and insist on functional exercise.

Exclusion criteria

Exclusion criteria: 1. Allergic to anesthetic drugs; 2. Patients with severe osteoporosis; 3. Complicated with serious circulatory, digestive, urinary and other diseases of the internal system; 4. Patients with diabetes, thyroid disease, stroke, hyperlipidemia, myocardial infarction, tuberculosis, emphysema and Parkinson's disease; 5. Those who are unable to cooperate due to mental and psychological diseases; 6. Patients with long-term fever due to skin breakage, ulceration or infection at the anesthetic puncture site; 7. Pregnant and lactating women; 8. Those who do not accept observation and do not want treatment; 9. Currently participating in other clinical trials; 10. Other conditions that the researcher considers inappropriate to join the study or undertake treatment.

Design outcomes

Primary

MeasureTime frame
Shoulder range of motion;Shoulder pain score;Shoulder function score;

Secondary

MeasureTime frame
Curative effect evaluation;Efficacy satisfaction;

Countries

China

Contacts

Public ContactWang Xiang

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine

w8x@163.com+86 13816985219

Outcome results

None listed

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