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Study on preemptive analgesia for repairing the rotator cuff with arthroscopic suture bridge technique

Study on preemptive analgesia for repairing the rotator cuff with arthroscopic suture bridge technique

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051413
Enrollment
Unknown
Registered
2021-09-23
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Disease of shoulder joint

Interventions

Experimental group:Anesthesia was given in advance during the operation
Control group:Do not give anesthetics in advance during the operation

Sponsors

Shanghai Changzheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 80 years; 2.Patients who intend to undergo arthroscopic rotator cuff suture bridge repair; 3.Agree to participate in this study.

Exclusion criteria

Exclusion criteria: 1.Emergency operation; 2.Open operation; 3.Neurological, cognitive or mental diseases, including stroke, dementia, and schizophrenia with language disorders, or any disease that makes a meaningful postoperative visit impossible; 4.Cardiovascular disease: defined as low-output heart failure with preoperative left ventricular ejection fraction < 30%, active coronary artery disease, severe valvular heart disease with shortness of breath, symptomatic arrhythmia, pacemaker arrhythmia or AICD placement; 5.Complicated with severe lung, liver and kidney dysfunction.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale;

Countries

China

Contacts

Public ContactZhu Yunli

Shanghai Changzheng Hospital

1434074814@qq.com+86 13917907968

Outcome results

None listed

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