跳至主要内容
临床试验/NL-OMON55672
NL-OMON55672招募中不适用

A prospective study to evaluate long-term clinical outcomes of the GTS cementless femoral stem - H36 GTS international

Zimmer Biomet0 个研究点目标入组 23 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
Zimmer Biomet
入组人数
23

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Male and non-pregnant females : >= 18 years and <= 70 years
  • 2. Patients requiring primary THR, suitable for the use of the GTS stem.
  • 3. The patient is diagnosed with osteoarthritis (OA) or avascular necrosis.
  • 4. The individual is physically and mentally willing and able to comply with
  • postoperative functional evaluation and able to participate in an appropriate
  • rehabilitation schedule.
  • 5. ASA classification score I-III.
  • 6. Patients who signed the Ethics Committee approved specific Informed Consent
  • Form prior to surgery.
  • 7. Surgical technique is planned to be Anterior Supine Intramuscular (ASI), or
  • patient has already received a GTS hip on the contralateral side.

排除标准

  • 1. Patients who had a THA on contralateral side more than 6 months ago and the
  • rehabilitation period outcome is considered unsatisfactory or not good.
  • (Patients with contra-lateral THA >6 months ago with good outcome (Harris Hip
  • Score >85) can be included in the study).
  • 2. Patients who had a THA on contralateral side less than 6 months ago.
  • 3. Patients with a major surgical procedure during the 12 weeks before the
  • study-related

研究者

发起方
Zimmer Biomet

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