Skip to content

Clinical Study on Multilayer Low-Elastic Bandage Combined with Conventional Rehabilitation for Promoting Functional Recovery After Knee and Ankle Surgery

Clinical Study on Multilayer Low-Elastic Bandage Combined with Conventional Rehabilitation for Promoting Functional Recovery After Knee and Ankle Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100566
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Postoperative swelling of lower limb injury

Interventions

Experience group:Multilayer Low-Elastic Bandage +Routine rehabilitation programs

Sponsors

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18–60 years; (2) Diagnosed with swelling, pain, and functional impairment after knee or ankle surgery; (3) Limb circumference increased by >2 cm or volume increased by >10% compared with the contralateral side; (4) No severe postoperative complications, with stable vital signs; (5) Signed informed consent and willingness to participate in the study.

Exclusion criteria

Exclusion criteria: (1) Severe complications (e.g., infection, deep vein thrombosis, neurovascular injury, etc.); (2) Other systemic diseases (e.g., severe cardiovascular, pulmonary, hepatic, or renal disorders); (3) Patients with cognitive impairment or mental illness who were unable to cooperate with the required treatments and assessments; (4) Patients with allergies to multilayer low-elastic bandage materials; (5) Limb infection or severe ulceration; (6) Use of any medication affecting body fluids and electrolytes; (7) Any other condition deemed by the investigator to render the subject unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
HSS score;kaikkonen;

Secondary

MeasureTime frame
VAS score;Reduction rate of affected limb edema;ROM;Strength;6-minute walk test ;SF-36 Quality of Life Questionnaire score;Proprioception;Center of plantar;

Countries

China

Contacts

Public ContactRong Xu

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School

hanxiaofeng202203@163.com+86 159 5193 5159

Outcome results

None listed

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