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A Multi-centre, Double-blind RCT to Investigate the Effect of Alendronate on Knee Function Following ACLR

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Enrollment target: 64 to 100 Primary completion date: Oct 31, 2025 to Jul 22, 2028 · Primary endpoints: 4 to 3 · Completion date: Dec 31, 2025 to Jul 22, 2028 · 3 morev4 Show 6 more changesShow less
    • Primary completion date: Oct 31, 2025 to Jul 22, 2028
    • Primary endpoints: 4 to 3
    • Completion date: Dec 31, 2025 to Jul 22, 2028
    • Interventions: Alendronate (ALN) (Drug) to Alendronate (ALN) (Drug), Placebo (Drug)
    • Eligibility criteria expanded, about 2 words
    • Study title expanded, about 1 word

    See this version in full on ClinicalTrials.gov ↗

  2. Notable Primary completion date: Oct 31, 2023 to Oct 31, 2025 Completion date: Dec 31, 2023 to Dec 31, 2025v3 Show 1 more changeShow less
    • Completion date: Dec 31, 2023 to Dec 31, 2025
  3. Notable Trial status: Not Yet Recruiting to Recruiting Start date changed from estimate of Nov 1, 2022 to Dec 22, 2022 · Site details revisedv2 Show 2 more changesShow less
    • Start date changed from estimate of Nov 1, 2022 to Dec 22, 2022
    • Site details revised
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05527548
Lead Sponsor Chinese University of Hong Kong
Conditions ACL Reconstruction
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov