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Observation of curative effect of suspended lower limb rehabilitation robot in early stage after anterior cruciate ligament reconstruction

Observation of curative effect of suspended lower limb rehabilitation robot in early stage after anterior cruciate ligament reconstruction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081492
Enrollment
Unknown
Registered
2024-03-04
Start date
2023-04-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Reconstruction of anterior cruciate joint of knee joint

Interventions

Control group:Conventional rehabilitation training
Experimental group:Conventional rehabilitation training+ Suspended lower limb rehabilitation robot

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients with simple and unilateral anterior cruciate ligament reconstruction; (2) Patients with ACL reconstruction or combined meniscus repair surgery; (3) Age 18-65 years old; (4) Patients who have a thorough understanding of the treatment plan and are willing to actively cooperate with the plan for diagnosis and treatment.

Exclusion criteria

Exclusion criteria: (1) Patients who require brace fixation after ACL reconstruction surgery; (2) Patients with preoperative ACL injury combined with intercondylar or tibial plateau fractures; (3) Patients with multiple ligament injuries such as posterior cruciate ligament and collateral ligament before surgery; (4) Combined hip or hip joint injuries; (5) Patients with poor healing of surgical incisions or postoperative infection of the knee joint; (6) Lower limb deep vein thrombosis; (7) Those who have severe internal diseases such as cardiovascular and cerebrovascular diseases and cannot cooperate with treatment; (8) Patients who do not agree to conduct experimental research or are unable to cooperate with treatment plans; (9) Participating in another clinical trial.

Design outcomes

Primary

MeasureTime frame
Knee joint pain score;Knee joint function score;

Secondary

MeasureTime frame
Range of motion of knee joint ;Degree of swelling in the knee joint;Human body composition testing;Quantitative testing of knee joint effusion;Inflammatory biochemical indicators;Lower limb circumference measurement;Adverse event;Satisfaction with clinical efficacy;Skin temperature;Emotional and Psychological Scale: SAS, SDS, Pain Catastrophizing Scale, Fair of Pain Questionnaire;

Countries

China

Contacts

Public ContactFang Fanfu

Shanghai Changhai Hospital

fangfanfu@126.com+86 158 0071 9913

Outcome results

None listed

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