A single-center, randomized controlled trial on the effect of short-term compression dressing on rehabilitation after primary total knee arthroplasty

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100052219

Enrollment

Unknown

Registered

2021-10-22

Start date

2021-10-06

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

knee osteoarthritis

Interventions

Experimental group:Compression dressing for 4 hours

Control group:Compression dressing for 24 hours

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with knee osteoarthritis who underwent primary unilateral total knee arthroplasty, aged approximately 18 years and < 80 years.

Exclusion criteria

Exclusion criteria: 1. The patient has a history of peripheral vascular disease, peripheral neuropathy, coagulation dysfunction, and deep vein thrombosis. 2. Severe valgus and varus knees require extensive soft tissue release.

Design outcomes

Primary

Measure	Time frame
Subjective feelings;Visual analogue scale;Circumference of knee joint;Circumference of thigh;Circumference of calf;Knee range of motion;''Stand up-walk'' timing test assessment;Pittsburgh sleep quality inventory;Epworth sleepiness score;	—

Countries

China

Contacts

Public ContactJiang Yunqi

Zhongshan Hospital, Fudan University

jiang.yunqi@zs-hospital.sh.cn+86 13817012898

Outcome results

None listed

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