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临床试验/NCT07560657
NCT07560657进行中(未招募)不适用

RHEVOLUTION Clinical Trial: Radial Head Arthroplasty for the Treatment of Acute Traumatic Elbow Instability, a Randomized Trial Comparing Two Implant Designs

Hospital Universitario La Paz1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2026年4月4日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
90
试验地点
1
主要终点
Mayo Elbow Performance Score (MEPS)

研究概览

简要总结

RHEVOLUTION Clinical Trial: Radial Head Arthroplasty for the Treatment of Acute Traumatic Elbow Instability, a Randomized Trial Comparing Two Implant Desings

Principal Investigator/collaborators: Dr. Raúl Barco, Dr. Blanca Diez Sánchez, Dr. Juan Ameztoy Gallego, Dr. Luis Palacios, Dr. Alfonso Vaquero-Picado and Dr. Samuel Antuña,

Department: Orthopedic Surgery and Traumatology Institution: La Paz University Hospital

Introduction: Participants are being invited to participate in a clinical research study. Our intention is to provide participants with clear and sufficient information so that participants may decide whether or not wish to participate. The investigators will answer any questions participants may have at any time. Participants may also discuss this information with anyone participants consider appropriate before making the decision.

Voluntary Participation: Participants' participation in this study is entirely voluntary. Participants may decide not to participate or withdraw the consent at any time without providing any explanation. Participants' decision will not affect the relationship with the doctor nor the medical care it is received in any way.

Study Description and Objectives: Participants are being invited to participate in a clinical study that aims to compare the outcomes of two elbow arthroplasties commonly used at our center to replace a portion of the elbow fractured by a fall that cannot be fixed. The fracture affects the radial head, and when fixation is not viable, the radial head is replaced with an arthroplasty.

Many different radial head arthroplasties have been designed to replace the bone, and overall, they have enabled patients with complex elbow fractures to regain mobility, stability, and return to sports activities at a level similar to before the fracture. However, some patients experience stiffness, nerve irritation, clicking sounds, or episodes of instability that they consider limiting in their lives. In these cases, it is sometimes necessary to remove the prosthesis if the symptoms are limiting.

Currently, although all prosthesis models have demonstrated good performance and achieve good results, the investigators do not know which design is best for each patient and type of fracture. The purpose of this study is to compare two types of radial head arthroplasties commonly used in La Paz Hospital for these fractures, to determine if they achieve similar clinical outcomes after 24 months of follow-up. The investigators want to analyze whether there are differences in satisfaction, range of motion, and functionality in patients operated on with one design or the other, with a stable elbow in both groups.

This is a randomized clinical trial, meaning that participants will be assigned to one of the two designs by chance (similar to flipping a coin). The operation will be the same for everyone, only the design of the arthroplasty used will change. One group of patients will receive an anatomic design (Align model from Skeletal Dynamics) and the other group will receive a spacer design (Evolve model from Stryker). Both procedures are performed by experienced surgeons and are safe.

Follow-up will include clinical and radiological examinations for at least 24 months after surgery. The clinical follow-up and treatment will be the same whether participants decide to get involved in the study or not, as all procedures correspond to standard clinical practice. Participants' medical care will not depend on participation in this study.

If participants decide to participate, it is necessary to sign an Informed Consent form. This study will be conducted at La Paz University Hospital and aims to include approximately 90 patients.

The study has been approved by the Research Ethics Committee in La Paz University Hospital in accordance with European Regulation 2017/745 and National Royal Decree 192/2023, which regulates medical devices.

Participants may not directly benefit from participating in this study. However, the results may contribute to improved knowledge regarding radial head fractures and arthroplasty in patients who had a complex elbow fracture.

Financial Compensation: The participation will not result in any additional cost to participants. No financial compensation will be provided.

Contact Information: If participants have any questions regarding the study, the use of medical data, or if participants have concerns or complaints related to the study, the contact will be:

Dr. Blanca Diez Sánchez, Dr. Juan Ameztoy Gallego or Dr. Raul Barco Laakso Telephone: +34 91 727 70 00 Ext. 47425

详细描述

Study Title: RHEVOLUTION Clinical Trial: Radial Head Arthroplasty for the Treatment of Acute Traumatic Elbow Instability, a Randomized Trial Comparing Two Implant Desings

Principal Investigator: Dr. Blanca Diez Sánchez, MD, PhD. Orthopaedic Department blanca.diez@salud.madrid.org Collaborators: Dr. Raúl Barco, Dr. Juan Ameztoy Gallego, Dr. Luis Palacios, Dr. Alfonso Vaquero-Picado and Dr. Samuel Antuña Institution: Hospital Universitario La Paz

  1. Abstract:

Study design: A randomized, parallel-group, single-blind clinical trial that will use two radial head arthroplasty designs (an anatomic design from Skeletal Dynamics and a smooth-stemmed spacer from Stryker) for the treatment of elbow fracture-dislocations. These two arthoplasty designs are already used in routine clinical practice at our center. However, patients are currently assigned one or the other based on availability and surgeon preference, not randomized. In the RHEVOLUTION clinical trial, patients will be randomly assigned to one radial head arthroplasty or the other, so that the patient (single-blind) will not know which implant they have received. There will be no active patient recruitment; instead, patients will be enrolled in the study if they meet the inclusion criteria and are referred consecutively to the department.

Inclusion criteria: Age over 18 years, acute, non-reconstructable radial head fracture, able to understand the informed consent and provide written consent and compliant with the planned clinical follow-up: at 6 weeks, 3 months, 6 months, 12 months, and 24 months. Only patients who underwent acute surgery using either of the two designs will be included.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age over 18 years
  • Acute, non-reconstructable radial head fracture scheduled for radial head replacement.
  • Able to understand the informed consent and patient information sheet and provide written consent.
  • Able to and compliant with the planned clinical follow-up: at 6 weeks, 3 months, 6 months, 12 months, and 24 months.
  • Underwent acute surgery, excluding treatment for sequelae.
  • Radial head replacement using either of the two study designs.

排除标准

  • Previous elbow surgeries or ligamentous or bone injuries managed conservatively.
  • Medical contraindications for surgery.
  • Medical comorbidities that may interfere with rehabilitation or participation in the study: advanced osteoarthritis, associated chondral lesions, advanced rheumatoid arthritis, neuromuscular or neurovascular disorders, chronic infections or immunodeficiencies, advanced cardiovascular, renal, or pulmonary disease, concurrent or past cancer
  • Allergy or contraindication to the use of prosthesis materials.

研究组 & 干预措施

Align radial head arthoplasty (Skeletal Dynamics)

Active Comparator

press-fit anatomic design

干预措施: Randomized selection of the implant used for surgery (Procedure)

Evolve radial head arthroplasty (Stryker Corporation)

Active Comparator

smooth-stem spacer

干预措施: Randomized selection of the implant used for surgery (Procedure)

结局指标

主要结局

Mayo Elbow Performance Score (MEPS)

时间窗: 24 months

The primary outcome of the study, corresponding to the main objective, will be the Mayo Elbow Performance Score (MEPS) at 24 months of follow-up. This score is measured using a validated, self-administered questionnaire that assesses pain, function, stability, and range of motion of the elbow. The scale ranges from 0 (worst) to 100 (best). The primary endpoint will be assessed as the average MEPS score for each intervention group at 24 months of post-intervention follow-up.

次要结局

  • Range of motion in flexion(24 months)
  • Range of motion in extension(24 months)
  • Range of motion in pronation(24 months)
  • Range of motion in supination(24 months)
  • Degree of pain(24 months)
  • Degree of satisfaction(24 months)
  • Grip strength(24 months)
  • Oxford Elbow Score(24 months)
  • Disabilities of the Arm, Shoulder and Hand Scale (Quick-DASH)(24 months)
  • Postoperative complications: infection(24 months)
  • Postoperative complications: neuropathies(24 months)
  • Postoperative complications: revision surgery(24 months)
  • Radiological analysis: implant malposition(6 weeks, 3 months, 6 months, 12 months and 24 months)
  • Radiological analysis: loosening(6 weeks, 3 months, 6 months, 12 months and 24 months)
  • Radiological analysis: stress shielding(6 weeks, 3 months, 6 months, 12 months and 24 months)
  • Radiological analysis: heterotopic ossifications(6 weeks, 3 months, 6 months, 12 months and 24 months)

研究者

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

Blanca Diez Sánchez, MD, PhD

Medical Doctor, PhD

Hospital Universitario La Paz

研究点 (1)

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