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Comparative Outcomes Between Foot Cast and Short Leg Cast in the Patients With Acute Closed Fracture of Proximal Fifth Metatarsal (Zone II)

Comparative Outcomes Between Foot Cast and Short Leg Cast in the Patients With Acute Closed Fracture of Proximal Fifth Metatarsal (Zone II)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03170687
Enrollment
72
Registered
2017-05-31
Start date
2017-01-24
Completion date
2018-09-01
Last updated
2018-09-18

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

Conditions

Acute Closed Fracture of Proximal Fifth Metatarsal (Zone II)

Brief summary

This study aims to compare outcomes of short leg cast and foot cast for treatment acute fifth metatarsal fracture (Zone II).

Detailed description

A randomized controlled trial will conducts between January 2017 and January 2019, participants with acute fifth metatarsal fracture (Zone II) will recruit for this study at the orthopedic outpatient clinic of a police general hospital, Bangkok, Thailand. A total of 100 patients will randomly allocate to receive foot cast or short leg cast. acute closed fracture of proximal fifth metatarsal (zone II) patients.

Interventions

DEVICEshort foot cast

metatarsal foot cast

full short leg cast

Sponsors

Police General Hospital
CollaboratorOTHER
Jatupon Kongtharvonskul
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

acute closed fracture of proximal fifth metatarsal (zone II) with following criteria 1. History of trauma and pain at lateral side of foot 2. Tenderness at base of 5th metatarsal 3. Radiographic finding shown fracture line at proximal 5th metatarsal bone

Exclusion criteria

1. more than 1 week 2. comminuted or multiple fracture 3. Open fracture 4. Ligament and tendon injury 5. Previous injury complication: nonunion, delayed union 6. Malignancy 7. refuse to inform consent

Design outcomes

Primary

MeasureTime frameDescription
VAS8 weeksvisual analog score

Secondary

MeasureTime frameDescription
AOFAS8 weeksfoot score
union rate8 weeksradiographic union
complication8 weeksskin ulcer or compartment syndrome

Other

MeasureTime frameDescription
rescue medication8 weeksparacetamol or NSAIDs

Countries

Thailand

Outcome results

None listed

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