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临床试验/NCT00587795
NCT00587795终止不适用

Orthopedic Study of the Aircast StabilAir Wrist Fracture Brace

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2006年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
Mayo Clinic
入组人数
1
试验地点
2
主要终点
Change in Distal Radius Fracture at 8 Weeks

研究概览

简要总结

Objectives:

  • To obtain clinical evidence for the safety and efficacy in using the StabilAir Wrist Fracture Brace for the following cases:
  1. Acute (emergency department) treatment of non-displaced, stable extra- articular distal radius fractures;
  2. To obtain comparative data between traditional therapies (sugar tong, plaster backslab, long arm or short arm cast) and the use of the StabilAir brace for each patient qualified by specific criteria.

Hypothesis:

  1. For stable, non-displaced fractures, the StabilAir Brace is as effective as a sugar tong splint in the acute setting. 2) In cases where full forearm immobilization is initially preferred, the StabilAir is effective as a follow-up to sugar tong splitting once the need for full immobilization has passed.

详细描述

Data Collection and Study Design:

This will be a single center, prospective, randomized controlled trial. The investigators planned to collect data from 80 patients with undisplaced distal radius fractures. Half were to be treated with the plastic back slab or sugar tong splint (if there were an ulnar styloid fracture) and half were to be treated with the StabilAir splint. The initial treatment, which was to occur upon the patient's arrival at the emergency room and prior to study randomization, required full forearm and wrist immobilization in the acute phase treated with sugar tong splinting. At the patient's follow-up visit, which was to happen ≤10 days post injury and initial evaluation, when it was determined that full forearm immobilization was no longer necessary, patients were informed of the study, consented, and randomized (as in the flip of a coin) to one of the two study groups using a computerized randomization process that was controlled by the study coordinator. One study group was to consist of patients treated with either sugar tong splint or plaster casting and the other study group was to consist of patients treated with the StabilAir brace. Throughout entire study, the sugar tong splint/casting patients was to be the control group.

Patients were to be asked to return for the following visits after they were randomized:

  • 10-14 days post randomization
  • 35 to 42 days (5 to 6 weeks) post randomization
  • 77 to 84 days (11 to 12 weeks) post randomization;
  • And at 12 and 24 months.

At each visit they were to have x-rays of their wrist and an exam with the physician. In addition, they were to be asked to complete questionnaires regarding their general health, daily activities and pain.

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

  • Males and Females Age ≥ 18 yrs
  • Undisplaced distal radial fractures (with/without ulnar styloid fractures)

排除标准

  • Age < 18 yrs
  • Intra-articular fracture - displaced
  • Loss of reduction after cast or brace treatment
  • Excessive comminution (> 50% metophysis)
  • Failed closed reduction (CR) (Unacceptable alignment status post CR: Short >2mm; Dorsal angulation >0° (neutral), Radial inclination < 15°)
  • Ipsilateral ulna fractures (not styloid)
  • Open fracture
  • Senile or dementia or lack of understanding of treatment
  • Previous fracture distal radius
  • Patients with displaced fractures that require pin fixation, external fixation, plate fixation or who qualify for "crystalline injection fracture healing protocol" are excluded from the study

研究组 & 干预措施

StabilAir Wrist Brace

Active Comparator

One study group will consist of patients treated with the StabilAir Wrist Brace.

干预措施: StabilAir Wrist Brace (Device)

Control

Placebo Comparator

Study arm will consist of patients that are treated with placement of sugar tong splint or plaster cast.

干预措施: Placement of sugar tong splint or plaster cast (Other)

结局指标

主要结局

Change in Distal Radius Fracture at 8 Weeks

时间窗: baseline, 8 weeks

The investigators planned to make radiographic assessments using the Stewart Score. The Stewart Score can range from 1 to 12, with a higher score indicating poor function: excellent (0), good (1-3), fair (4-6) and poor (7-12).

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

David Dennison

PI

Mayo Clinic

研究点 (2)

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