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Comparing Short-term Function and Pain After No Treatment or Splinting for Boxer's Fracture

Comparing Short-term Function and Pain After No Treatment or Splinting for Boxer's Fracture

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02547181
Enrollment
40
Registered
2015-09-11
Start date
2014-09-30
Completion date
2018-01-31
Last updated
2016-10-24

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

Conditions

Metacarpal Fractures

Keywords

Fracture, Follow-up, metacarpal

Brief summary

This Study is being done because the investigators would like to know if pain and hand function after having a boxer's fracture differs between being treated with supportive splinting or without splinting, but with behavioral modifications.

Detailed description

After initial treatment in the emergency department, patients with boxer's features are referred to the division of plastic and reconstructive surgery at Sunnybrook hospital. During initial consultation with the hand surgeon, treatment is chosen. Patients are follow-up with their hand surgeon at 4-, 8-, and 12--week intervals. Supportive splinting: Patient's are given a removable plaster/fiberglass splint with a tensor bandage underneath. Behavioral Modifications: Patients are not splinted, but provided a tensor bandage. Patients are instructed on specific behaviours to prevent movement of the injured part of the hand. The purpose of the study is to compare pain and short-term hand function in patients who undergo supportive splinting compared to patients who undergo behavioral modifications treatment only to see which option is associated with shorter functional recovery and which option is associated with less pain during the first 4 weeks after initial treatment. On follow-up appointments at 4, 8,and 12 weeks, as well as initial consultation with the hand surgeon, participants will be asked to perform a grip strength test with a Jamal Hydraulic hand Dynanometer. Participants will be asked to fill out a Brief Michigan Hand Questionnaire along with the grip strength test as well as quick demographics survey at initial consultation with the hand surgeon. After the 12-week follow up appointment, study participation will end. If a patient is unable to follow-up with the hand surgeon, the Brief Michigan Hand Questionnaire will be done via phone whenever is most convenient for the patient. It's anticipated that about 40 people will participate in this study at a single centre in Toronto.

Interventions

Patient will be provided with tensor bandage and instructed on specific behaviors to prevent movement of the injured part of the hand.

BEHAVIORALSplint

fibreglass splint

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Diagnosis of true boxer's fracture * Candidate for either supportive splinting or tensor bandage * Speaking, read and write English

Exclusion criteria

* Prior surgical treatment for boxer's fractures or other hand conditions. * Concurrent hand/wrist injury

Design outcomes

Primary

MeasureTime frameDescription
hand function4 weeksmeasured by Brief Michigan Hand Questionnaire (MHQ)

Secondary

MeasureTime frameDescription
Grip strength4 weeksmeasured using Dynamometer

Countries

Canada

Contacts

Primary ContactCatherine McMillan, MSc
Catherine.mcmillan@sunnybrook.ca

Outcome results

None listed

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