Treatment Clinical Trial
Official title:
Hard-soled Shoe Versus Short Leg Walking Cast for a Fifth Metatarsal Avulsion Fracture: A Randomized Multicenter Noninferiority Trial
Fifth metatarsal avulsion fractures are common and can usually be treated conservatively.
Symptomatic care consisting of protected weightbearing in a hard-soled shoe, air-cast
walking boot, or below-knee walking cast have been successful. Several papers reported that
early rehabilitation may decrease ankle stiffness, muscle and bone atrophy, and aids in
early return to activities. However, early motion of the ankle joint may have the risk of
displacement of the fifth metatarsal avulsion fractures. However, studies using hard-sole
shoe for protected weightbearing and allowing motion of the ankle joint had successful
results. Clapper et al. compared the results of hard-soled shoe and walking cast for a fifth
metatarsal avulsion fracture and reported that all avulsion fractures healed uneventfully
and that the results were similar between the two. However, this was not a randomized
controlled trial.
Devices such as air-cast walking boot, plaster slipper, or Jone's dressing can also be used
for the treatment. However, we decided to compare results of hard-soled shoe and short leg
walking cast for the treatment of a fifth metatarsal avulsion fracture.
We hypothesized that the 100mm visual analogue scale (VAS) assessed on 6 months after a
fifth metatarsal avulsion fracture treated with protected weightbearing in a hard-soled shoe
is not inferior to protected weightbearing in a short leg walking cast but is superior to
short leg walking cast with respect to time to return to normal daily life and patient's
satisfaction.
This study is a noninferiority, randomized controlled trial of patients presenting to
multiple centers. The primary outcome measure is the 100mm VAS assessed on 6 months after a
fifth metatarsal avulsion fracture. 100mm VAS was compared between the experimental group
(hard-soled shoe) and the control group (short leg walking cast) on 6 months follow-up
examination. The 100mm VAS is widely used self assessment tool for evaluating pain after
fracture. The secondary objectives were to determine whether hard-soled shoe was superior to
short leg walking cast with respect to time until return to normal daily life and patient's
satisfaction.
The sample size was determined using methods appropriate for noninferiority trials, assuming
90% power and a significance level of 0.05. We performed a pilot study on 18 patients and
assessed 100mm VAS on 6 months. Pooled standard deviation was 16.6. To find out whether the
hard-soled shoe is not inferior to short leg walking cast for a fifth metatarsal avulsion
fracture, 74 patients were required to have 90% power that the lower limit of an one-sided
95% confidence interval for the difference between two treatments will be above the
noninferiority margin of -10. We assumed the drop-out rate to be 20%. Adding this number, 96
patients were required for the study.
Determination of the noninferiority margin was based on clinical significance. Todd et al.
reported on a study of 48 patients that the minimum clinically significant difference of
100mm VAS was 13mm and that differences of less than this amount, even if statistically
significant, are unlikely to be of clinical significance. We decided that the noninferiority
margin at 10 mm difference which is less than this amount will be adequate to prove
noninferiority of the experiment group (hard-soled shoe) over the control group (short leg
walking cast).
After 1 weeks of immobilization in a short leg posterior splint, patients are randomized to
experiment group (hard-soled shoe) and control group (short leg walking cast). Randomization
was stratified by the study centers. Block randomization were used and the investigators
were blinded to the block sizes being used to ensure allocation concealment. Delayed union
was defined as a lack of bridging callus on 3 of 5 cortices at 12 weeks. Nonunion was
defined as lack of cortical bridging or a clearly visible fracture line, at 14 weeks post
injury.
If a subject had discontinued prior to completion of 6 months, the last observation was
carried forward for the intent-to-treat analysis. Subjects who crossed over to the other
treatment arm, for an example, patients in experiment group(hard-soled shoe) who changed to
short leg walking cast or in control group (short leg walking cast) who changed to
hard-soled shoe, were analyzed according to their initial group allocation for the
intent-to-treat analysis. Additionally, an as-treated (per-protocal) analysis was also
conducted on patients who completed the 6 months follow-up with the protocol assigned.
Although previous studied have not documented an increase risk of reduction loss with
protected weightbearing in a hard-soled shoe protocol, a safety rule was put in place to
assure patients, clinicians, and the health research ethics board that the safety of our
patients was a priority. Reduction loss was not a primary outcome, but it was monitored
carefully regardless of published evidence. A safety rule established a priori eliminated
any dissent among the research team and participating surgeons about stopping the study in
the event of an apparent adverse outcome related to protected weightbearing in a hard-soled
shoe. If a difference of greater than three spontaneous reduction loss occurred between the
groups, the intervention would be halted. A reduction loss or metal failure was defined as
one that occurred without patient instigation of inappropriate activity. The reduction loss
was to be monitored by study personnel not involved in the outcome assessment.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05243134 -
The Influence of Anatomic Deformities on the Clinical Efficacy in the Patients With Patellar Dislocation
|
||
Completed |
NCT02486874 -
Clinical Evaluation of PoreSkin
|
Phase 1 | |
Active, not recruiting |
NCT04592640 -
Stem Cells for Uremic Calciphylaxis Patients
|
N/A | |
Recruiting |
NCT04599686 -
Stereotactic Body Radiotherapy (SBRT) for Oligometastatic Prostate Cancer
|
N/A | |
Recruiting |
NCT03351842 -
Surgery With or Without Chemotherapy for Stage I NSCLC With Micropapillary Component ≥ 20%
|
Phase 2 | |
Completed |
NCT02782442 -
Cognitive Training Delivered Remotely to Individuals With Psychosis (ROAM)
|
N/A | |
Completed |
NCT03439930 -
The Effect of Balance Training on Neuromuscular Control in Subjects With CAI
|
N/A | |
Not yet recruiting |
NCT05537155 -
Buccal Acupuncture for Delirium Treatment in Older Patients Recovering From Orthopedic Surgery
|
N/A | |
Recruiting |
NCT02971982 -
PCD Versus RCD for the Treatment of Patients With Waldenstrom's Macroglobulinemia
|
Phase 1/Phase 2 | |
Completed |
NCT02820272 -
Water for Reducing Pain in Negative Pressure Wound Therapy
|
Phase 2 | |
Completed |
NCT00984958 -
Bulkamid Treatment of Stress Incontinence in Women With Urinary Stress Incontinence and Not Suitable to TVT-procedure
|
N/A | |
Completed |
NCT00575224 -
Pegasys and Copegus for Asian Patients With Treatment-naive Hepatitis C Genotypes 6, 7, 8, 9
|
Phase 4 | |
Completed |
NCT00164307 -
Assisting Children With Prenatal Alcohol Exposure in Developing Peer Friendships
|
Phase 1/Phase 2 | |
Completed |
NCT00164528 -
Intervening With Children/Adolescents With FAS/ARND
|
Phase 1/Phase 2 | |
Recruiting |
NCT04603586 -
Stereotactic Radiotherapy in Locally Advanced Pancreatic Cancer With Different Biological Effective Doses
|
N/A | |
Recruiting |
NCT03375424 -
Vedolizumab Study With Inflammatory Bowel Disease Patients in Germany
|
N/A | |
Not yet recruiting |
NCT04062370 -
Ranibizumab Treatment for Macular Edema Secondary to Retinal Vein Occlusion
|
Phase 4 | |
Not yet recruiting |
NCT02931136 -
Early Diagnosis and Early Treatment of Alzheimer's Disease Based on Senile Plaque Imaging
|
Phase 4 | |
Completed |
NCT04661228 -
Diagnostic Survey of Mental and Substance Use Disorders in HUNT (PsykHUNT)
|
||
Recruiting |
NCT03365141 -
Efficacy of Intralesional Triamcinolone Injection in the Treatment of Vitiligo
|
N/A |