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Study on clinical anesthesia pathway for arthroscopic rotator cuff repair

Study on clinical anesthesia pathway study for Arthroscopic Shoulder Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072110
Enrollment
Unknown
Registered
2023-06-02
Start date
2022-01-02
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

Anesthesia for arthroscopic rotator cuff repair

Interventions

Sponsors

Sichuan Provincial Orthopedic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled for elective unilateral Arthroscopic Shoulder Surgery; 2. Aged 40 to 59 years, regardless of gender; 3. American Society of Anesthesiologists (ASA) Physical Status classification I to II; 4. Body mass index was not less than 19kg/?, and not more than 30 kg/?; 5. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who had bleeding diathesis or who had using anticoagulant; 2. Preexisting hypertension, coronary heart disease and other cardiovascular diseases; 3. Preexisting diabetes mellitus and hyperlipidemia; 4. Allergy to local anesthetics, or contraindications to peripheral nerve block;

Design outcomes

Primary

MeasureTime frame
the duration of elevated pressure irrigation;surgeon satisfaction with the surgical field visibility;

Secondary

MeasureTime frame
Duration of operation;Edema of neck tissue;Edema of chest tissue;The occurrence of pulmonary edema;irrigation volume;PaO2 and PaCO2;SPO2 and PH;PaO2/FiO2;Hct and HB;

Countries

China

Contacts

Public ContactLi Su

Sichuan Provincial Orthopedic Hospital

309565338@qq.com+86 180 9630 5451

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026