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Clinical study on the treatment of frozen shoulder by manipulation under brachial plexus anesthesia

Clinical study on the treatment of frozen shoulder by manipulation under brachial plexus anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006033
Enrollment
Unknown
Registered
2022-05-24
Start date
2019-06-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Frozen Shoulder

Interventions

The control group:Celecoxib combined with functional exercise
Experimental group:Manual release under brachial plexus anesthesia combined with functional exercise

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 between 40 and 70; (2) In line with the diagnostic criteria of Frozen Shoulder, shoulder joint activity was significantly limited; (3) Before treatment, MRI of shoulder joint was taken to exclude perishoulder tendon and ligament rupture, rotator cuff injury, tumor and other intraarticular or organic lesions; (4) Outpatient review for more than 3 months and insist on functional exercise.

Exclusion criteria

Exclusion criteria: In any of the following circumstances, it cannot be included in this test: (1) Those who do not meet the inclusion criteria; (2) allergic to narcotic drugs; (3) shoulder pain and mobility disorders mainly caused by cervical spondylosis, some connective tissue diseases and obvious skin contracture after burns and scalds around the shoulder; (4) complicated with serious heart, liver, kidney, blood and other internal diseases; (5) the existence of depression, mania and other mental and psychological diseases; (6) Patients with long-term fever and skin damage, ulceration or infection at the anesthesia puncture site; (7) Pregnant women and lactating women; (8) those who refuse observation or treatment; (9) currently participating in other clinical trials; (10) Other conditions that the investigator considers inappropriate for inclusion in this study or treatment.

Design outcomes

Secondary

MeasureTime frame
Range of motion of shoulder joint(including flexion, extension, abduction, pronation, extension and internal pronation);"Simple Mcgill" pain Scale;

Primary

MeasureTime frame
Constant-Murley shoulder function score;

Countries

China

Contacts

Public ContactWang xiang
w8x@163.com13816985219

Outcome results

None listed

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