Condition or disease | Intervention/treatment | Phase |
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Ankle Fractures | Other: Postoperative protocol (Immediate weight bearing) Other: Postoperative Protocol (Delayed Weight Bearing) | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 25 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | Diabetic patients with ankle fractures will be manage operatively and then randomized to be prescribed a hindfoot offloading brace 2 weeks after surgery or be randomized to follow a non-immediate weight bearing rehabilitation protocol |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Immediate Vs. Delayed Weight Bearing Postoperative Protocol in Diabetic Ankle Fractures |
Actual Study Start Date : | August 1, 2020 |
Estimated Primary Completion Date : | June 15, 2025 |
Estimated Study Completion Date : | June 15, 2025 |
Arm | Intervention/treatment |
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Experimental: Hindfoot Offloading Braces / Immediate Weight-bearing
Diabetic patients over 18 years of age who sustained an isolated (non-pilon) ankle fracture will undergo ORIF of the ankle fracture within 3 weeks of the event
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Other: Postoperative protocol (Immediate weight bearing)
After ORIF of the ankle fracture, the patient will be randomized to follow an immediate weight bearing rehabilitation protocol using an offloading hindfoot brace
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Placebo Comparator: No Hindfoot Offloading Braces / Delayed Weight-Bearing
Diabetic patients over 18 years of age who sustained an isolated (non-pilon) ankle fracture will undergo ORIF of the ankle fracture within 3 weeks of the event
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Other: Postoperative Protocol (Delayed Weight Bearing)
After ORIF of the ankle fracture, the patient will be randomized to follow a standard delayed weight-bearing rehabilitation protocol
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Adverse Events by type over time, severity, seriousness, and relatedness. AEs will be tabulated and summarized as counts and percentages. AEs will also be cross-tabulated according to:
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Stacee W Clawson, RN | (573) 884-9017 | clawsons@health.missouri.edu | |
Contact: Ennio Rizzo Esposito, MD | 3468126445 | eardvb@health.missouri.edu |
United States, Missouri | |
University of Missouri Health System | Recruiting |
Columbia, Missouri, United States, 65212 | |
Contact: Stacee Clawson, BSN, RN 573-884-9017 clawsons@health.missouri.edu |
Principal Investigator: | Kyle M Schweser, MD | Assistant Professor Orthopaedic Trauma/Foot and Ankle |
Tracking Information | |||||||||
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First Submitted Date ICMJE | May 24, 2019 | ||||||||
First Posted Date ICMJE | May 29, 2019 | ||||||||
Last Update Posted Date | September 18, 2020 | ||||||||
Actual Study Start Date ICMJE | August 1, 2020 | ||||||||
Estimated Primary Completion Date | June 15, 2025 (Final data collection date for primary outcome measure) | ||||||||
Current Primary Outcome Measures ICMJE |
Adverse Events [ Time Frame: 12 months ] Adverse Events by type over time, severity, seriousness, and relatedness. AEs will be tabulated and summarized as counts and percentages. AEs will also be cross-tabulated according to:
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Original Primary Outcome Measures ICMJE | Same as current | ||||||||
Change History | |||||||||
Current Secondary Outcome Measures ICMJE |
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Original Secondary Outcome Measures ICMJE |
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Current Other Pre-specified Outcome Measures | Not Provided | ||||||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||||||
Descriptive Information | |||||||||
Brief Title ICMJE | Immediate Vs. Delayed Weight Bearing Postoperative Protocol in Diabetic Ankle Fractures | ||||||||
Official Title ICMJE | Immediate Vs. Delayed Weight Bearing Postoperative Protocol in Diabetic Ankle Fractures | ||||||||
Brief Summary | Operatively managed diabetic ankle fractures have significant risk for complications. The cause for failure is likely multifactorial, however, a component of failure has to do with an inability to process pain and pressure normally. This loss of protective sensation allows for an increase in abnormal stresses placed on the recently repaired fractures. Historically, diabetics have been kept non weight bearing for extended periods of time, which has its own functional and cardiovascular issues. The purpose of the study is to determine if a protocol of immediate weight bearing with a hindfoot offloading brace after surgically corrected ankle fracture in a diabetic patient will maintain adequate motion, have no difference in complications when compared to regular non-immediate weight bearing protocols, and lead to good outcome scores and patient satisfaction scores | ||||||||
Detailed Description |
Operatively managed diabetic ankle fractures have significant risk for complications. The cause for failure is likely multifactorial, however, a component of failure has to do with an inability to process pain and pressure normally. This loss of protective sensation allows for an increase in abnormal stresses placed on the recently repaired fractures. Historically, diabetics have been kept non weight bearing for extended periods of time, which has its own functional and cardiovascular issues. The purpose of the study is to determine if a protocol of immediate weight bearing with a hindfoot offloading brace after surgically corrected ankle fracture in a diabetic patient will maintain adequate motion, have no difference in complications when compared to regular non-immediate weight bearing protocols, and lead to good outcome scores and patient satisfaction scores Patients will be recruited from the trauma and foot & ankle service lines. Patients who have experienced an isolated ankle fracture (excluding pilon fracture) and will undergo operative fixation within 3 weeks of injury will be approached for consent. Patients will then be screened based on the inclusion and exclusion criteria. Up to 25 patients will be enrolled The following protocol will be applied after enrollment
1. Placement into short leg, non-weight bearing splint to allow for wound healing and brace fabrication ii. Research Specific: 1. Fitted for brace (will be custom made and take approximately 1-2 weeks) b. 2 week visit (standard of care timepoint) i. Standard of Care:
1. Placement into brace so it offloads the hindfoot to 15 pounds of pressure or less 2. Education by prosthetist, physiatrist, and/or attending physician about proper brace wear and maintenance, and the importance of weight bearing only in brace. c. 3 Week visit (not standard of care timepoint) i. Research Specific 1. Ankle radiographs d. 4 weeks, 6 weeks, 12 Weeks, 26 weeks, and 1 year visits (standard of care time points) i. Standard of Care
1. Counseling regarding brace wear 2. Brace adjustments as needed e. 8 week, 10 week, 14 week, 16 week, (non-standard of care biweekly visits until healing occurs) i. Research Specific
Upon study completion, patients will continue with post-operative rehab following the surgeon's standard of care. If a patients is removed prematurely or if the study ends prematurely, they will receive standard of care procedures going forward |
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Study Type ICMJE | Interventional | ||||||||
Study Phase ICMJE | Not Applicable | ||||||||
Study Design ICMJE | Allocation: Randomized Intervention Model: Parallel Assignment Intervention Model Description: Diabetic patients with ankle fractures will be manage operatively and then randomized to be prescribed a hindfoot offloading brace 2 weeks after surgery or be randomized to follow a non-immediate weight bearing rehabilitation protocol Masking: None (Open Label)Primary Purpose: Treatment |
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Condition ICMJE | Ankle Fractures | ||||||||
Intervention ICMJE |
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Study Arms ICMJE |
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Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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Recruitment Information | |||||||||
Recruitment Status ICMJE | Recruiting | ||||||||
Estimated Enrollment ICMJE |
25 | ||||||||
Original Estimated Enrollment ICMJE | Same as current | ||||||||
Estimated Study Completion Date ICMJE | June 15, 2025 | ||||||||
Estimated Primary Completion Date | June 15, 2025 (Final data collection date for primary outcome measure) | ||||||||
Eligibility Criteria ICMJE |
Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender ICMJE |
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Ages ICMJE | 18 Years and older (Adult, Older Adult) | ||||||||
Accepts Healthy Volunteers ICMJE | No | ||||||||
Contacts ICMJE |
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Listed Location Countries ICMJE | United States | ||||||||
Removed Location Countries | |||||||||
Administrative Information | |||||||||
NCT Number ICMJE | NCT03966027 | ||||||||
Other Study ID Numbers ICMJE | 2014997 | ||||||||
Has Data Monitoring Committee | No | ||||||||
U.S. FDA-regulated Product |
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IPD Sharing Statement ICMJE |
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Responsible Party | Kyle Schweser MD, University of Missouri-Columbia | ||||||||
Study Sponsor ICMJE | Kyle Schweser MD | ||||||||
Collaborators ICMJE | Not Provided | ||||||||
Investigators ICMJE |
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PRS Account | University of Missouri-Columbia | ||||||||
Verification Date | September 2020 | ||||||||
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |