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A Study on the Efficacy of Manual Release Combined with New Rapid Rehabilitation Strategy under Sedation and Analgesia in the Treatment of Shoulder Periarthritis

A Study on the Efficacy of Manual Release Combined with New Rapid Rehabilitation Strategy under Sedation and Analgesia in the Treatment of Shoulder Periarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112882
Enrollment
Unknown
Registered
2025-11-20
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

periarthritis of shoulder

Interventions

Traditional group:After the patient received manual release treatment under sedation and analgesia, routine anti-inflammatory and anti-swelling symptomatic treatment was administered, and guidance was
Analgesic pump group:After the patient received the same manual loosening techniques and routine anti-inflammatory and anti-swelling treatment, a new rapid recovery strategy was implemented, including

Sponsors

The Second Affiliated Hospital of Xiamen Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients were diagnosed with frozen shoulder according to the criteria in the "Guidelines for Clinical Diagnosis and Treatment of Orthopedic and Traumatic Diseases in Traditional Chinese Medicine: Periarthritis of the Shoulder," and met the following inclusion criteria: aged between 45 and 70 years, disease duration of more than one month, no severe underlying conditions such as heart disease, neurological disorders, or coagulation dysfunction, and voluntarily participated in this study by signing an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Shoulder X-ray examination to exclude patients with shoulder fractures or dislocations, and MRI examination to exclude patients with rotator cuff injuries of grade three or above, as well as those with tendon ruptures; 2. Patients who have received other invasive shoulder treatments in the past half month; 3. Shoulder pain caused by other reasons; 4. Patients with local skin infections in the treatment area, blood system diseases, mental illnesses who cannot cooperate with treatment, or contraindications to invasive procedures.

Design outcomes

Primary

MeasureTime frame
Shoulder joint range of motion measurement form;Numerical Rating Scale;Pittsburgh Sleep Quality Index;Changes in the medication regimen;

Countries

China

Contacts

Public ContactZhang Guanghui

The Second Affiliated Hospital of Xiamen Medical College

372499021@qq.com+86 159 6003 6903

Outcome results

None listed

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