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临床试验/NCT02505932
NCT02505932已完成不适用

Latarjet Procedure: Comparative Outcomes Study of Arthroscopic Versus Mini-open Approach With Minimum 2-year Follow-up

Hospital Ambroise Paré Paris2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2012年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
58
试验地点
2
主要终点
Average postoperative shoulder's pain on visual analogic scale from 0 (no pain) to 10 (maximum pain)

研究概览

简要总结

To date, use of arthroscopic procedure to perform Latarjet procedure is still technically demanding. The benefits of arthroscopic procedure need to be evaluated compared to the mini-invasive approach. The aim of this study was to assess postoperative pain during the first week, and the positioning of coracoid bone block at the anterior aspect of the glenoid. At minimum 2 years follow-up, the recurrence of shoulder instability and functional evaluation of patients according to the Western Ontario Score Index (WOSI) were assessed.

详细描述

This prospective comparative study was performed at two centers in 2012. Each center performed one procedure so this study was observational. All patients with a chronic anterior instability requiring bone grafting (Instability Severity Index Score>3) were included. The Latarjet procedure was performed by mini-open approach (set Arthrex, Naples, FL) in the first group, and by arthroscopic approach (set Depuy-Mitek, Raynham, MA) in the second group. The analgesic postoperative protocol was standardized (paracetamol, non-steroidal anti-inflammatory, tramadol).

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • chronic anterior instability requiring bone grafting (Instability Severity Index Score>3)

排除标准

  • Patient refusal

结局指标

主要结局

Average postoperative shoulder's pain on visual analogic scale from 0 (no pain) to 10 (maximum pain)

时间窗: Average during the first week

次要结局

  • Functional evaluation of patients(2-year minimal follow-up)
  • Recurrence rate of shoulder instability (number of recurrence/total number of patients)(2-year minimal follow-up)
  • Mean daily pain on visual analogic scale from 0 (no pain) to 10 (maximum pain)(Daily from day1 to day7)
  • analgesic consumption (Number of pills)(Daily from day1 to day7)
  • presence of postoperative discomfort symptoms (yes/no)(Daily from day1 to day7)
  • coracoid bone block position to the anterior aspect of the glenoid on the anterior-posterior and the lateral X-ray and on CT-scan(Between 3 to 6 months follow-up)

研究者

发起方
Hospital Ambroise Paré Paris
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shahnaz Klouche, MD

Physician responsible of clinical research

Hospital Ambroise Paré Paris

研究点 (2)

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