跳至主要内容
临床试验/NCT04049279
NCT04049279招募中不适用

Migration in Total Hip Arthroplasty with a Cemented BiMobile Cup: Better Stability with More Cement? (Be-Mobile)

JointResearch2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
2
主要终点
Migration of the acetabular cup

研究概览

简要总结

Objective: The main objective of this study is to compare the (early) migration of the cemented BiMobile cup at two year post-surgery between two different cup sizes after standard optimal reaming, and consequently adjusting the cement mantle into circa 2 or 4 mm, in patients with a primary cemented total hip arthroplasty (THA). Additionally, the results of the BiMobile cup will be compared to the Avantage cup, which is placed with a standard cup size, resulting in a cement mantle of approximately 2 mm.

Study design: A prospective single centre blinded randomised controlled trial.

Study population: All patients who meet the criteria to undergo a cemented THA.

详细描述

Rationale: Total hip arthroplasty (THA) is a commonly performed surgery in patients with end-stage osteoarthritis (OA) of the hip. Although it is known as a successful procedure, (recurrent) dislocation after THA is a major problem and results in a deterioration in quality of life. Dislocation after THA is the number one cause of early revision surgery.

Dual-Mobility (DM) acetabular cups should provide more stability and biomechanically reduce the risk of (early) dislocation. Potential disadvantages of DM cups are increased liner wear, psoas impingement and loosening. This might result in more revision surgery at mid- and longer-term follow-up for the cemented cups. If the cemented fixation technique improves, this might diminish the disadvantages of more revisions due to loosening in cemented cups. High quality evidence guiding the best technique for cemented fixation is however lacking. The risk of implant loosening might be reduced by increasing the amount of cement used for cup fixation. It is currently unknown whether size of the implant, and thereby the amount of cement, affects stability and survival. To fill this gap in knowledge, this study will compare cup migration, as an indicator for loosening, in a new dual mobility cup (BiMobile, Waldemar Link GmbH & Co. KG, Hamburg, Germany), using a larger or smaller cup size (and thereby different amounts of cement: approximately 2mm or 4mm cement mantle). These results will also be compared with the Avantage cup (ZimmerBiomet), which is yet considered as a standard dual mobility cup in the Netherlands. Migration will be measured with Rontgen Stereophotogrammetry Analysis (RSA), which is currently the gold standard for measuring early migration and predicting long term survival. A relatively new and less intensive way to measure migration of prostheses is the use of computer tomography (CT) scans, however there is still little scientific evidence on how accurately this can be done. This study therefore also measures the accuracy with which migration is measured, between CT scans and RSA.

Objective: The main objective of this study is to compare the (early) migration of the cemented BiMobile cup at two year post-surgery between two different cup sizes after standard optimal reaming, and consequently adjusting the cement mantle into circa 2 or 4 mm, in patients with a primary cemented THA. Additionally, the results of the BiMobile cup will be compared to the Avantage cup, which is placed with a standard cup size, resulting in a cement mantle of approximately 2 mm.

Study design: A prospective single centre blinded randomised controlled trial.

Study population: At the outpatient clinic of OLVG, all patients who meet the criteria to undergo a cemented THA will be screened for the in- and exclusion criteria.

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
Single (Participant)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient requiring an elective primary cemented THA.
  • Male patient ≥70 years old and female patient ≥65 years old.
  • Ability and willingness to follow instructions and to return for follow-up evaluations.
  • The patient is able to understand the meaning of the study and is willing to sign informed consent.
  • Understanding the Dutch language.

排除标准

  • The patient is morbidly obese, defined as Body Mass Index (BMI) of ≥
  • The patient is expected to need lower limb joint replacement for another joint within one year.
  • The patient has a systemic or metabolic disorder leading to progressive bone deterioration.
  • The patient has a deformity or disease located in other joints than the hip that needs surgery and that is limiting their ability to walk.
  • The patient has an active or suspected latent infection in or around the hip joint.
  • The patient's bone stock is compromised by a disease or infection which cannot provide adequate support and/or fixation to the prosthesis.
  • The patient is unable or unwilling to sign informed consent for this study.
  • The patient is deemed unsuitable for participation in the study based on the investigator's judgment.

结局指标

主要结局

Migration of the acetabular cup

时间窗: 2 years postoperative

Migration of the acetabular cup, measured with rontgen stereophotogrammetry analysis (RSA).

次要结局

  • Patient reported outcomes on physical functioning(prior to surgery, 6 months, 1 year, 2 years and 5 years after surgery)
  • Patient reported outcomes on quality of life.(prior to surgery, 6 months, 1 year, 2 years and 5 years after surgery)
  • Migration of the acetabular cup(6 weeks, 6 months and 1 year postoperative)
  • Patient Satisfaction(prior to surgery, 6 months, 1 year, 2 years and 5 years after surgery)
  • Patient reported outcomes on pain(prior to surgery, 6 months, 1 year, 2 years and 5 years after surgery)

研究者

发起方
JointResearch
申办方类型
Other
责任方
Sponsor

研究点 (2)

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