Effect of different place anesthesia on analgesia after total knee arthroplasty

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000033810

Enrollment

Unknown

Registered

2020-06-13

Start date

2020-07-01

Completion date

Unknown

Last updated

2020-06-15

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

Conditions

Total knee arthroplasty

Interventions

Group 1:posterior and side infiltration anesthesia group

Group 2:anterior infiltration anesthesia group

Eligibility

Sex/Gender

All

Age

50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of knee osteoarthritis; 2. Unilateral initial TKA; 3. Varus deformity of knee joint < 25 degrees, varus deformity < 15 degrees. 4. American doctors' association (ASA) class for I - II.

Exclusion criteria

Exclusion criteria: 1. Having a definite mental or mental illness; 2. Previous knee fracture or operation history; 3. Abnormal muscle strength or activity of lower limbs caused by history of cerebrovascular disease or neurological disease; 4. Intolerance to Tramadol; 5. No subcutaneous congestion around the joint; 6. Related complications occurred after operation.

Design outcomes

Primary

Measure	Time frame
VAS;KSS;	—

Secondary

Measure	Time frame
WOMAC;Tramadol dosage;	—

Countries

China

Contacts

Public ContactBo Zhang

Beijing Chaoyang Hospital

chaoyangyiyuan2020@126.com+86 010-85231653

Outcome results

None listed

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