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The impact of preoperative blood flow restriction training on postoperative pain and knee joint function following anterior cruciate ligament reconstruction: a prospective, randomized, parallel-controlled study

The impact of preoperative blood flow restriction training on postoperative pain and knee joint function following anterior cruciate ligament reconstruction: a prospective, randomized, parallel-controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088027
Enrollment
Unknown
Registered
2024-08-09
Start date
2024-08-31
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Anterior cruciate ligament injury

Interventions

Blood flow restriction training group:Undergoing blood flow restriction training
Control group:none

Sponsors

China-Japan Union Hospital of jilin university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Participants aged between 18 and 50 years old (inclusive), of any gender, with mature skeletal structure and closed epiphyses. (2) Diagnosis of planned ACL tear confirmed through clinical examination and MRI within the past 8-10 weeks; no prior history of ACL injury in the involved or contralateral limb with reconstruction. (3) Stable vital signs and normal liver and kidney function. (4) Body Mass Index (BMI) between 18 and 35. (5) Not participated in any other clinical trials within the past 3 months. (6) Participants fully understand the benefits and risks of the trial, voluntarily agree to participate, and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Lower limb conditions such as skin lesions, ulceration, swelling, soft tissue injuries, and vascular damage. (2) Bleeding disorders. (3) Severe primary diseases affecting cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems. (4) Patients with abnormal mental behavior who cannot cooperate. (5) Recent use of specific medications such as antiepileptic drugs, immunosuppressants, etc. (6) Inability to undergo preoperative rehabilitation training. (7) Blood pressure >200/110 mm Hg or <90/60 mm Hg. (8) Complete knee joint dislocation or need for repair of structures within the knee joint other than the ACL and meniscus. (9) Other reasons deemed unsuitable by researchers, such as inability to assess efficacy, etc.

Design outcomes

Primary

MeasureTime frame
VAS score ;HSS score;IKDC ligament score;

Secondary

MeasureTime frame
complications;patient satisfaction;Quadriceps strength, quadriceps morphology, knee flexion angle;Postoperative inflammatory indicators;

Countries

China

Contacts

Public Contactzuo jianlin

China-Japan Union Hospital of Jilin University

zuojl@jlu.edu.cn+86 178 0807 1178

Outcome results

None listed

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