跳至主要内容
临床试验/NCT07335133
NCT07335133
招募中
不适用

Short- and Medium-term Postoperative Complications of Ankle Arthroscopy

Clinique Saint Jean, France1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2026年1月5日最近更新:

概览

阶段
不适用
状态
招募中
发起方
Clinique Saint Jean, France
入组人数
150
试验地点
1
主要终点
Complications occurring within one year following ankle arthroscopy

概览

简要总结

The goal of this clinical trial is to describe complications that occurred in the year following surgery, based on follow-up surgical consultations and physical therapy sessions.

The target population is any adult patient who has undergone ankle surgery performed under arthroscopy.

Primary outcome is description of all complications occurring within one year following ankle arthroscopy. This description will be based on clinical and functional examinations performed by surgeons and physical therapists.

Participants will be regularly monitored by the surgeon and physical therapist (15 days postoperative, 3 months, 6 months, and 1 year).

They will complete self-assessment questionnaires and undergo functional physical therapy tests, including ALR RSI, FAAM AVQ, FAAM Sport, CAIT, and Ankle Go.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

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

  • Adult patient who has been informed and has signed the consent form
  • Patient scheduled for arthroscopic ankle surgery.
  • Patient affiliated with or covered by a health insurance plan

排除标准

  • Recent traumatic injury (less than 1 month old), physical therapy assessment impossible
  • Inability to follow up for up to one year
  • Patient under legal protection
  • Pregnant woman, patient under guardianship or conservatorship
  • Patient who has already undergone ankle surgery

结局指标

主要结局

Complications occurring within one year following ankle arthroscopy

时间窗: One year

Description of all complications occurring within one year following ankle arthroscopy. This description will be based on clinical and functional examinations performed by surgeons and physical therapists.

次要结局

未报告次要终点

研究者

发起方
Clinique Saint Jean, France
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wayan HEBRARD

Principal Investigator

Clinique Saint Jean, France

研究点 (1)

Loading locations...

相似试验