跳至主要内容
临床试验/NCT05736640
NCT05736640已完成不适用

The Effect of Denosumab on Periprosthetic Bone Mineral Density in Six Transfemoral Amputees Treated With Osseointegrated Implants: The Observations From a Terminated Randomized Controlled Trial

University of Aarhus0 个研究点目标入组 6 人开始时间: 2013年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
6
主要终点
change in periprosthetic bone mineral density

研究概览

简要总结

Femur amputated patients often suffer from several problems with conventional socket prosthesis. Some experience changes in gait, discomfort when sitting, altered skin conditions (infection, irritation, rashes, sweat), phantom pain or lack of stabilization between the prosthesis and the residual limb. Many have a low score on "health-related quality of life" questionnaires (HRQL).

Some femur amputated patients may be a candidate to osseointegrated prosthesis. Osseointegrated prosthesis is an implant, where the fixture is inserted into the femur canal and an abutment screw, on which the leg-prostheses is inserted, protrudes the skin. By this procedure the patient have a high score on HRQL and experience fewer problems. They have improved gait, reduced discomfort when sitting, increased prosthetic use, and experience fewer skin and pain problems.

Femur amputee patients formerly mobilized on socket prosthesis have a reduced bone mineral density in the affected femur and pelvis.

The Phd-theses compromise of three studies. The aim of the first study is to follow patients with oosseointegrated prosthesis before and after surgery with DXA-scans to monitor the BMD. In the second study patients will be randomised to receive medical treatment with an RANKL-inhibitor, approved for treatment of osteoporosis, and monitored with DXA, microdialysis and radiostereometry. Depending on the DXA-results patients in the third study may receive fast track rehabilitation.

The hypothesis is that patients with osseointegrated prosthesis will have an increased BMD after surgery, 2 years follow up. Patients receiving RANKL inhibitor will have increased BMD, stability of the prosthesis, and some receive fast-track rehabilitation due to high BMD.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18-70 years
  • Scheduled for OI-implant surgery
  • Body mass index <30
  • Female patients of childbearing age must produce a negative pregnancy test and use effective contraception
  • informed consent

排除标准

  • Diabetes with complication
  • Atherosclerosis
  • Drug abuse
  • Treatment with NSAID or cytostatic
  • Active cancer
  • Liver or kidney insufficiency
  • Hip flexion contracture on the affected side >10 degrees
  • Body weight >100 kg
  • Hypocalcaemia
  • Contraindications to denosumab

研究组 & 干预措施

Denosumab

Active Comparator

干预措施: Denosumab (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

change in periprosthetic bone mineral density

时间窗: 30 months po

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

相似试验