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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02779244
Other study ID # 16-00720
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date July 1, 2023

Study information

Verified date November 2023
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this randomized, controlled trial is to estimate the safety of early weight bearing on post ankle surgery. Patients who are indicated to have surgery for unstable ankle fractures by an attending trauma physician will be consented for participation in the study. After surgery patients will be randomized to either weight bearing as tolerated at two weeks with a cam boot or non-weight bearing with a cam boot. Randomization will be performed by number allocation with odd numbers in the early weight bearing group and even numbers in the non-weight bearing group. The surgeon will be blinded to this until after the surgery. The patients will all be placed in a short leg cast post operative and made non-weight bearing for 2 weeks until sutures are removed which is current standard treatment. Both groups will be asked to initiate weight bearing at two weeks post operatively by wearing a cam boot that is non weight bearing in a cam boot, the latter being standard treatment.


Recruitment information / eligibility

Status Completed
Enrollment 107
Est. completion date July 1, 2023
Est. primary completion date June 14, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Operative unstable ankle fractures Exclusion Criteria: - Requirement of syndesmotic fixation - Pilon fractures - Open fractures - Patients with diabetic neuropathy - BMI>40 - Polytrauma patients - Patients who are unable to comply with non-weight bearing - Patients who are unable to follow up

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Early Weight bearing + Cam Boot
Patients will be transitioned to weight bearing as tolerated in a cam boot.
Non-Weight Bearing + Cam Boot
Subject will be transitioned to non weight bearing cam boot, standard treatment.

Locations

Country Name City State
United States New York University Langone Medical Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Olerud Molander Ankle Score The Olerud Molander score is scored between 0 - 100 as painless and functionally perfect ankle. 1 year
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