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临床试验/NCT06727344
NCT06727344招募中不适用

Comparison of Conservative Treatment With Blood Flow Restriction With Standard Management in Total ACL Rupture. "Randomized Clinical Trial"

European University Cyprus1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
1
主要终点
Strength

研究概览

简要总结

The goal of this randomised clinical trial is to evaluate the effects of exercise with blood flow restriction (BFR) in patients with a complete anterior cruciate ligament (ACL) rupture.

The main questions it aims to answer are:

  1. Does blood flow restriction adds any additional benefits to conservative treatment of the ACL?
  2. Does bracing promotes spontaneous healing to the ACL

Researchers will compare bracing and BFR to bracing and sham BFR to see if the intervention provides any additional benefits to the conservative management of this injury.

Participants will:

  1. Use a knee brace for 6 weeks with adjustments according to protocol
  2. Follow and identical exercise plan with either BFR (intervention group) or BFR sham (control group)
  3. Follow a home based exercise program.

详细描述

Methodological design:

For the purposes of the present study, a double-blind, two-arm randomised clinical trial will be conducted. Participants in the intervention group will undergo and exercise protocol with the use of blood flow restriction (BFR). Participants in control group will follow the same exercise protocol but with sham BFR instead. Both groups will follow the same brace protocol.

Intervention group:

The intervention group will consist of people with a recent ACL tear who meet the eligibility criteria. Participants in this group will follow a splint use protocol. In particular, during the first 3 weeks (phase 1) a splint will be used with the knee immobilised at 90°, non-weight bearing walking with the use of walking aids according to age and mobility. During the 4th and 5th week (phase 2) the range of motion of the splint will be set to 60° to 90° and from 30° to 90° respectively. Walking will remain non-weight bearing. During the 6th week (phase 3) the degree of freedom of the splint will be placed at 0° allowing full flexion but preventing hyperextension of the joint. During this phase, partial bearing is allowed with the use of a walking aid. From the 7th week (phase 4) onwards the splint is removed and walking is done with no loading restrictions.

Regarding the exercise program, participants in this group, during phase 1, will perform isometric quadriceps and hamstring contractions guided by a visual stimulus from an electronic hand dynamometer. The exercise parameters will be 75 repetitions divided into 4 sets (30,15,15,15) at 30% of the 1st maximum of the opposite leg. During phase 2, the exercise protocol is maintained as phase 1 with the only differences that the exercises will be performed at 60 degrees too. Additionally, the "sliding" exercise will be added where the heel is dragged on the bed causing knee flexion as well as the skateboard sliding exercise from a seated position in the allowed range of motion. Exercise parameters remain the same for all exercises as previous phase. In the 3rd phase, single leg squats up to 45° are added. Exercise parameters remain the same. In the 4th phase, the exercise protocol changes. Subjects start at a stationary bike for 5 minutes (without BFR) and the quadriceps and hamstrings isometrics are replaced with resistance exercises for extension and knee flexion. Sliding and single-leg squats are performed at an increased range of flexion (up to 90°) and climbing a 30cm step is added. All exercise parameters remain the same as in the previous phases. During the last phase (5th) gait retraining on a treadmill for 5 minutes and Y balance exercise is added. Both of these exercises will be performed without BFR. The break between sets will be 30 seconds and between exercises 1 minute.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •MRI-confirmed complete rupture of ACL. Ability to communicate and read fluently in Greek and be willing to keep their leg immobilised for the required period based on the study protocol.

排除标准

  • •Heart disease, overweight, diabetes, pregnancy, thrombophilia, atrial fibrillation, heart failure, cancer, use of drugs that may increase blood clotting, use of hormones or contraceptives, any reason for not using BFR e.g., an open wound or serious skin problems and/or allergies to the cuff material.

研究组 & 干预措施

Brace and BFR exercise

Experimental

干预措施: Blood Flow Restriction (Other)

Brace and BFR exercise

Experimental

干预措施: Brace (Other)

Brace and BFR sham

Sham Comparator

干预措施: Brace (Other)

结局指标

主要结局

Strength

时间窗: Enrolment, week 2 and 4, end of intervention (12 weeks)

Quadriceps strength using a hand held dynamometer

次要结局

  • MRI(Enrolment and end of intervention at 12 weeks)
  • Knee laxity(enrolment and end of intervention at 12 weeks)
  • Balance(enrolment and end of intervention at 12 weeks)
  • Swelling(enrolment and end of intervention at 12 weeks)
  • Visual analog scale (VAS)(enrolment, week 2 and 4 and end of intervention at 12 weeks)
  • Lysholm scale(enrolment and end of intervention at 12 weeks)
  • Patient reported outcome measures(enrolment and end of intervention at 12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alexios Pitsillides

Alexios Pitsillides BSc, MSc, PhD (cand)

European University Cyprus

研究点 (1)

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