Skip to content

Effect analysis of preoperative Blood Flow Restriction training combined with postoperative CPM in elderly patients after total knee arthroplasty

Effect analysis of preoperative Blood Flow Restriction training combined with postoperative CPM in elderly patients after total knee arthroplasty

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094134
Enrollment
Unknown
Registered
2024-12-17
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Arthritis of the knee

Interventions

experimental group:Preoperatively, in addition to routine care, pressurised resistance training was used, i.e., knee extension and straight leg raising exercises were performed while using a pressuris
control subjects:Preoperatively, he received routine care without compression training, and postoperatively, he received routine rehabilitation training, including CPM . The CPM machine was started on

Sponsors

The Third Bethune Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Subjects aged 65 years or older (including 65 years old), gender is not limited; (2) Blood pressure 90/60 mm Hg, normal liver and kidney function; (3) Body mass index 18 <= BMI <= 30; (4) Pre-existing unilateral primary total knee arthroplasty; (5) Have not participated in other clinical trials within 3 months; (6) Subjects are fully aware of the benefits and risks of this trial and are still willing to participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Lower limbs with skin breakdown, history of deep vein thrombosis or potential deep vein thrombosis, vesicular swelling, soft tissue injury and vascular injury; (2) Suffering from bleeding disorders or coagulation disorders; (3) Comorbidity with serious primary diseases such as cardiovascular, cerebrovascular, hepatic, renal and haematopoietic systems; (4) Patients with abnormal mental behaviour who cannot cooperate; (5) Those who have recently taken special drugs, such as antiepileptic drugs and immunosuppressants; (6) Those who cannot accept long-term postoperative rehabilitation training; (7) Others who are not suitable for enrolment in the opinion of the investigators, such as those who cannot perform efficacy judgement.

Design outcomes

Primary

MeasureTime frame
pain ;Range of motion; knee function;

Secondary

MeasureTime frame
Degree of swelling (knee circumference);Muscle strength;Ability to live in daily living;C-reactive protein;

Countries

China

Contacts

Public ContactQiheng Zhao

THE THIRD BETHUNE HOSPITAL OF JILIN UNIVERSITY

zhaoqh@jlu.edu.cn+86 139 4418 8035

Outcome results

None listed

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