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Orthopedic Study of the Aircast StabilAir Wrist Fracture Brace

Orthopedic Study of the Aircast StabilAir Wrist Fracture Brace

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00587795
Enrollment
1
Registered
2008-01-07
Start date
2006-04-30
Completion date
2008-11-30
Last updated
2017-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Radius Fractures

Brief summary

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.

Detailed description

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.

Interventions

DEVICEStabilAir Wrist Brace

Patient will be placed in a StabilAir Wrist Brace 10-14 days after initial injury and return for follow up visits at 6 weeks; 3, 6, 12 and 24 months.

OTHERPlacement of sugar tong splint or plaster cast

Patients will receive a sugar tong splint or plaster cast for their wrist fracture. They will return for x-rays and an exam at 6 weeks; 3, 6, 12 and 24 months.

Sponsors

AirCast LLC
CollaboratorINDUSTRY
Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Change in Distal Radius Fracture at 8 Weeksbaseline, 8 weeksThe 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).

Countries

United States

Participant flow

Recruitment details

One subject was recruited from the Mayo Clinic in Rochester, Minnesota in 2007.

Participants by arm

ArmCount
StabilAir Wrist Brace
One study group will consist of patients treated with the StabilAir Wrist Brace. StabilAir Wrist Brace: Patient will be placed in a StabilAir Wrist Brace 10-14 days after initial injury and return for follow up visits at 6 weeks; 3, 6, 12 and 24 months.
1
Control
Study arm will consist of patients that are treated with placement of sugar tong splint or plaster cast. Placement of sugar tong splint or plaster cast: Patients will receive a sugar tong splint or plaster cast for their wrist fracture. They will return for x-rays and an exam at 6 weeks; 3, 6, 12 and 24 months.
0
Total1

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyWithdrawal by Subject10

Baseline characteristics

CharacteristicStabilAir Wrist BraceControlTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
1 Participants0 Participants1 Participants
Age, Categorical
Between 18 and 65 years
0 Participants0 Participants0 Participants
Region of Enrollment
United States
1 participants1 participants
Sex: Female, Male
Female
0 Participants0 Participants
Sex: Female, Male
Male
1 Participants1 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 10 / 0
other
Total, other adverse events
0 / 10 / 0
serious
Total, serious adverse events
0 / 10 / 0

Outcome results

Primary

Change in Distal Radius Fracture at 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).

Time frame: baseline, 8 weeks

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026