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Effects of anaesthesia method and tourniquet use on recovery following joint arthroplasty: a randomised controlled study

Effects of anaesthesia method and tourniquet use on recovery following joint arthroplasty: a randomised controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042075
Enrollment
Unknown
Registered
2021-01-13
Start date
2021-01-12
Completion date
Unknown
Last updated
2021-04-19

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

Conditions

joint arthroplasty

Interventions

Spinal anesthesia plus tourniquet group:Spinal anesthesia plus tourniquet
Spinal anesthesia without tourniquet group:Spinal anesthesia without tourniquet
General anesthesia plus tourniquet group:General anesthesia plus tourniquet
No tourniquet is added to general anesthesia:No tourniquet is added to general anesthesia

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: We included consenting patients, aged 18-75 years, with BMI 40 kg/m2, ASA physical status class I-III, severe knee osteoarthritis (Kellgrene Lawrence grade III-IV), failure of conservative treatment, and eligibility for joint arthroplasty.

Exclusion criteria

Exclusion criteria: We excluded patients with prior major surgery, severe malalignment of the target knee, or severe flexion or extension deficits. Other reasons for exclusion were contraindication to the studys medication or anaesthesia regimen, ongoing use of strong opioids, and a need for bridging anticoagulation. We excluded patients who were unable to understand written study information in China.

Design outcomes

Primary

MeasureTime frame
Analgesic depletion;Hemoglobin;Pain;Transfusion rate;Hospital complications;Hospital stays;Blood;

Countries

China

Contacts

Public ContactFeng Shuo

Affiliated Hospital of Xuzhou Medical University

xzfs0561@163.com+86 18552880088

Outcome results

None listed

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