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临床试验/NCT05527548
NCT05527548招募中4 期

The Effect of Oral Administration of Alendronate on Knee Functions Following Anterior Cruciate Ligament Reconstruction - A Multi-Centre, Double-Blind, Placebo-Controlled, Randomized Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年12月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
100
试验地点
1
主要终点
Single-leg Hop Test (SLH)

研究概览

简要总结

Anterior cruciate ligament (ACL) is the key ligament connecting the femur to tibia that helps stabilising the knee joint. ACL tear is common. It accounts for over 50% of all knee injuries and affects more than 200,000 people in the United States each year. Patients with ACL tear have a higher risk of developing post-traumatic osteoarthritis. ACL reconstruction (ACLR) with the attachment of tendon grafts within bone tunnels are commonly performed to restore the stability of the joint and thereby minimise injury to both the chondral surface and surrounding tissues. About 130,000 ACLR was performed in the United States in 2006. Both the incidence rates of ACL injuries and ACLR are on the rise, particularly in children and adolescents. Conventional ACLR is not a universally successful procedure, with long healing time and high rates of graft failure (2.8%) and graft laxity (18%). The average cost of an ACLR in the United States was about USD 24,707 ±15,644. The cost for revision surgery and societal cost due to absence from work and sport are expected to be even higher. The demand for a better intervention to improve the outcomes after ACLR and reduce the healing time is huge.

ALN was chosen for the pilot study because it is the most studied BPs, with high bone-binding affinity and more prolonged duration of action. As a member of amino BPs, it also has higher anti-resorptive activities compared to non-amino BPs. Our encouraging results on ALN in the animal studies also provide evidence to support the trial of ALN in human.

ALN have been shown to have a very good safety and tolerability profile. The common side effects of ALN are stomach pain, constipation, diarrhoea, gas, or nausea. Oral ALN seems can induce mild gastro-intestinal disturbances. However, two studies, with subjects treated with ALN for 10 months and 2.9 years, respectively, showed that ALN was not associated with any increased incidence of upper GI tract events. The serious adverse event, oesophageal cancer, has been associated with ALN. However, two published papers with long term observations of 9 and 4.5 years, respectively, showed that ALN was not significantly associated with incident oesophageal or gastric cancer compared with the control group.

This study aims to evaluate the effects of oral administration of ALN on knee stability (primary), peri-tunnel bone loss, tunnel bone formation, knee laxity, knee muscle strength as well as self-reported knee symptoms, function and sports activity over 12 months in patients undergoing ACLR in a pilot study of single-blind randomised controlled trial.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
14 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Male and female with age 14 or above at the time of surgery
  • •First ACLR
  • •Single leg involvement
  • •Able to attend pre-operative assessment
  • •Voluntarily agreed to participate and signed the informed consent form

排除标准

  • •Known chronic disease or receiving long-term medications affecting bone metabolism including BPs
  • •Contraindication to alendronate therapy such as poor dental fitness
  • •ACL injury less than 6 weeks
  • •Injury on duty cases
  • •Patients who have undergone arthroscopy or open surgery in the index knee in the last 12 months
  • •Other associated injuries (fractures and other ligament involvement such as neurovascular bundles injury)
  • •Chondral lesion with concomitant intervention
  • •Presence of X-ray features of osteoarthritis including decrease in joint space, presence of osteophytes and subchondral cysts
  • •Neurological deficit
  • •Pregnant or breastfeeding
  • •Inability to give informed consent

研究组 & 干预措施

PCB Group

Placebo Comparator

patients receive weekly dose of placebo and a standard rehabilitation program

干预措施: Placebo (Drug)

ALN group

Experimental

Patients receive weekly dose of 70mg of ALN and a standard rehabilitation program

干预措施: Alendronate (ALN) (Drug)

结局指标

主要结局

Single-leg Hop Test (SLH)

时间窗: Change from baseline SLH at 4.5 months

SLH test measures the functional stability of the knee with high intraclass correlation coefficients ranging from 0.97 to 0.99 (59). The patient will be asked to perform single-leg hop on both the injured and non-injured legs three times and the hop distance will be recorded. An index score, calculated by dividing the averaged hop distances of the injured leg by that of the non-injured leg, will be reported.

Single-leg Hop Test (SLH)

时间窗: Change from baseline SLH at 6 months

SLH test measures the functional stability of the knee with high intraclass correlation coefficients ranging from 0.97 to 0.99 (59). The patient will be asked to perform single-leg hop on both the injured and non-injured legs three times and the hop distance will be recorded. An index score, calculated by dividing the averaged hop distances of the injured leg by that of the non-injured leg, will be reported.

Single-leg Hop Test (SLH)

时间窗: Change from baseline SLH at 12 months

SLH test measures the functional stability of the knee with high intraclass correlation coefficients ranging from 0.97 to 0.99 (59). The patient will be asked to perform single-leg hop on both the injured and non-injured legs three times and the hop distance will be recorded. An index score, calculated by dividing the averaged hop distances of the injured leg by that of the non-injured leg, will be reported.

次要结局

未报告次要终点

研究者

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

Pauline Lui

Professor

Chinese University of Hong Kong

研究点 (1)

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