Unna Boots for Ankle Fracture Swelling

Sponsor
Medical University of South Carolina (Other)
Overall Status
Withdrawn
CT.gov ID
NCT04086927
Collaborator
(none)
0
2
11

Study Details

Study Description

Brief Summary

This study will evaluate the difference in soft tissue swelling prior to surgery and wound complications after surgery between unna boot application versus standard splint application. An unna boot is an extra zinc covered wrap around your leg followed by standard splint application (cotton dressing, plaster, then soft dressing). Prior to surgery the participant's swelling will be measured and compared to the standard splint application group. After surgery, the participant will be monitored for wound complications, pain, and range of motion.

Condition or Disease Intervention/Treatment Phase
  • Device: Unna Boot
N/A

Detailed Description

The purpose of this study is to compare preoperative swelling and frequency of wound complications in ankle fractures through standard splint and an unna boot compressive dressing with a splint. Quantitative and qualitative measurements will be analyzed to compare edema and wound complications. Secondary goals are to evaluate the quantitative differences in ankle range of motion and visual analogue scale (VAS) pain scores. The hypothesis of this proposed study is that there will be less soft tissue swelling and wound complications with the use of an unna boot when compared to the standard splint. The investigators also hypothesize that there will be improved ankle range of motion and visual analogue scale (VAS) pain scores with the use of an unna boot when compared to a standard splint. Participants will be randomized to either the standard splint or an unna boot and quantitative and qualitative measures will be collected. This data could change the practice for preoperative management of soft tissue swelling following ankle fractures.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Unna Boot: A Technique to Decrease Preoperative Soft Tissue Swelling Following Ankle Fractures
Anticipated Study Start Date :
Jan 31, 2021
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Group

Patients will not receive compression dressing

Experimental: Experimental Group

Patients will receive compression dressing

Device: Unna Boot
The unna boot is a zinc coated compression dressing

Outcome Measures

Primary Outcome Measures

  1. Baseline swelling using Figure-8 Measurement [Baseline (Initial encounter)]

    Physician uses tape measure to measure angles to determine swelling severity of ankle. This measurement is taken by making a figure eight pattern on the foot and ankle. The measurement is taken three times and then averaged to give the final total.

  2. Mean swelling using Figure-8 Measurement [6 weeks follow up visit]

    Physician uses tape measure to measure angles to determine swelling severity of ankle. This measurement is taken by making a figure eight pattern on the foot and ankle. The measurement is taken three times and then averaged to give the final total.

  3. Mean pain scores on visual analogue scale at initial encounter [Baseline (initial encounter)]

    patients report a pain score of 1-10. 1 being the lowest and 10 being the highest

  4. Mean pain scores on visual analogue scale at 6 week follow up visit [6 weeks follow up visit]

    patients report a pain score of 1-10. 1 being the lowest and 10 being the highest

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • acute ankle fracture
Exclusion Criteria:
  • low energy ankle fracture

  • open ankle fracture

  • unwillingness to participate

  • allergy to zinc

  • revision surgery

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Medical University of South Carolina

Investigators

  • Principal Investigator: Christopher E Gross, M.D., Orthopaedic Surgeon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT04086927
Other Study ID Numbers:
  • 00092143
First Posted:
Sep 12, 2019
Last Update Posted:
Jan 12, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 12, 2021