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Ankle Sprain clinical trials

View clinical trials related to Ankle Sprain.

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NCT ID: NCT04095598 Recruiting - Ankle Sprain Clinical Trials

Computed Tomography With Stress Maneuvers for Evaluation of Distal Tibiofibular Syndesmosis Instability (CTMETS)

CTMETS
Start date: September 1, 2018
Phase:
Study type: Observational

The main aim of this study was to investigate which strategy can diagnose more accurately syndesmotic instability among an existing index test (ankle CT in neutral position) and two new add-on index tests (ankle CT in a stress position with extended-knees and ankle CT in a stress position with flexed-knees). This study hypothesized that the two add-on ankle CT with stress maneuvers (CTSM) have a more accurate capability of diagnosing syndesmotic instability than ankle CT in a neutral position (CTNP) alone. The secondary objective is to investigate the participants' disability outcomes by applying the Foot and Ankle Ability Measure questionnaire.

NCT ID: NCT02945618 Recruiting - Ankle Sprain Clinical Trials

Neurocryostimulation for Acute Lateral Ankle Sprain

Start date: June 2015
Phase: N/A
Study type: Interventional

The objective of this exploratory randomized control trial is to compare, in participants with acute lateral ankle sprain (LAS) , the reduction of symptoms and functional limitations between two groups of subjects who undergo a conventional rehabilitation program with (experimental group) or without CRYOFOS (comparison group). The hypothesis is that CRYOFOS will lead to a faster reduction of symptoms and functional limitations, and a faster return to daily living activities.Thirty-six participants of 18 years of age and older with acute LAS (sustained a LAS three days or less before the first evaluation session) will be recruited and randomly assigned to either a group receiving conventional rehabilitation program with the addition of CRYOFOS (experimental group; n=18), or to a group only receiving the conventional rehabilitation program (comparison group; n=18). This single-blind (evaluator), parallel-group RCT will include five evaluation sessions over 6 weeks (baseline, day 7, week 2, week 4 and week 6) and 8 treatment sessions (1st and 2nd weeks: 3 sessions/week; 3rd and 4th weeks: 1 session/week) during a 4-week period. The primary outcome will be the functional limitations, evaluated using the Lower Extremity Functional Scale (LEFS).

NCT ID: NCT02491736 Recruiting - Ankle Sprain Clinical Trials

Ketoprofen Gel vs Placebo in Children With Ankle Sprain

Start date: June 2015
Phase: Phase 4
Study type: Interventional

The aim of this study is to analyse the effect of ketoprofen gel in children presented with ankle sprain to the emergency department.

NCT ID: NCT01117909 Recruiting - Ankle Sprain Clinical Trials

Effects of Talocrural Joint Mobilizations in the Treatment of Subacute Lateral Ankle Sprains

Start date: April 2010
Phase: N/A
Study type: Interventional

The goal is to determine if standard therapy including joint mobilizations of the ankle performed 3 times per week for 2 weeks will increase self-reported function and decrease pain in patients with mild lateral ankle sprains.