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Ankle Injuries clinical trials

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NCT ID: NCT02276339 Completed - Ankle Injuries Clinical Trials

Muscle Activation in Chronic Ankle Instability and the Effect of an Exercise Programme

Start date: October 2014
Phase: N/A
Study type: Interventional

This study aims to investigate the activity patterns of the peroneal muscle group, in individuals with a history of chronic ankle instability (CAI) of the ankle injuries compared with individuals without ankle problems. The study also aims to determine the effect of a targeted exercise programme on this muscle group in patients with CAI. Research on this topic may provide important insight on the roles of these muscles in chronic ankle instability and investigate whether specific strengthening programmes are effective in this complex patient category.

NCT ID: NCT02252276 Completed - Ankle Sprains Clinical Trials

Effects of Manual Therapy and Exercise in the Treatment of Ankle Sprains

Start date: January 2014
Phase: N/A
Study type: Interventional

Objectives: To analyze the effects of proprioceptive and strengthening exercises versus the same exercises and manual therapy on the recurrent ankle sprain management. Design: A randomized clinical trial with two intervention groups and triple blind. Settings: University Hospital. Participants: Fifty-four patients with previous history of recurrent ankle sprains, regular sports practice and pain during the physical activity, randomly assigned to experimental or control group. Intervention: Control group performed 4 weeks of proprioceptive and strengthening exercises; experimental group performed 4 weeks of the same exercises combined with manual therapy. Main Outcomes Measures: Pain, ankle instability, pressure pain threshold (PPT), ankle eversion strength, and active range of motion in ankle joint. The measures were taken before, after and one month after the interventions.

NCT ID: NCT02187406 Completed - Ankle Injuries Clinical Trials

Ankle Athletic Taping Fatigue After a Standard Tennis Warm up

Start date: June 2014
Phase: N/A
Study type: Interventional

Identify, quantify and compare the fatigue caused in two ankle athletic tapes after the completion of a tennis warm-up.

NCT ID: NCT02115217 Completed - Clinical trials for Sprain and Strain of Ankle

Effect of Kinesiotaping on Ankle Stability

Start date: February 2014
Phase: N/A
Study type: Interventional

Ankles sprains are the most popular injuries in basketball players. They are traumatic injuries, which happen most of the time in specific situations, like landing on another player's foot, or during changes of direction. Neuromuscular exercises are very important to improve ankle stability and reduce risks of sprains. However various external support such as ankles braces and rigid tape, are also used in order to prevent injury. The kinesiotape (KT) is a new but broadly used method in the world of athletes. Created by KenzoKase, in 1980, this kind of tape has a tremendous success with athletes and is today commonly used during practices and/or competitions. The main property of this tape is its elasticity, which is supposed to improve proprioception and, thus ankle stability, but these aspects have not been investigated yet.

NCT ID: NCT02100670 Completed - Pain Clinical Trials

A Multicenter Efficacy Study of a Diclofenac+Menthol Gel in Subjects With Ankle Sprain

Start date: November 1, 2013
Phase: Phase 3
Study type: Interventional

This Phase III pivotal efficacy study will assess efficacy and onset of pain relief of MFC51123 gel vs. placebo and MFC51123 gel vs. 1% diclofenac gel and 3% menthol gel in participants with an ankle sprain to support topical MFC51123 gel registration.

NCT ID: NCT02097940 Completed - Ankle Sprain Clinical Trials

Influence of Sensorimotor Treatment in the Balance of Soccer

Start date: March 2014
Phase: N/A
Study type: Interventional

This study presents the hypothesis that the sensory processing engine improves balance and agility for football athletes.

NCT ID: NCT02091674 Completed - Ankle Sprain Clinical Trials

Management of Acute Ankle Sprain With Sodium Hyaluronate

Start date: August 2013
Phase: Phase 2
Study type: Interventional

To determine the efficacy and safety of hyaluronic acid (AdantTM, Tedec-Meiji Farma SA) for acute ankle sprain, a single-site, open-label, controlled trial will be conducted. The study will be conducted in a sport-medicine clinical research center in London, Ontario, Canada. The eligible patients will be 18 years of age and older, have first or second degree lateral sprain within 48h of the start of the treatment, and moderate or severe pain (>45mm on 100 mm pain visual analogue scale /VAS). Exclusion criteria will include bilateral ankle sprain, ipsilateral knee trauma, prior sprain in the past 6 months, use of NSAID prior to entry, intra-articular ankle injection in the prior 6 months. The patients will receive standard care (RICE and rescue analgesics), and a single 2.5cc Adant periarticular ankle injection following provision of informed consent and collection of baseline data. NSAIDs, corticosteroids or topical analgesics will not be allowed. Assessments will be done at baseline, days 8, 30 and day 90. Efficacy measures will include patient's pain VAS on weight bearing (0-100mm) and walking 20m (0-100mm), patients' global assessment of ankle injury (5 point categorical scale), patients' assessment of normal function/activity (5 point categorical scale), physician's global assessment of ankle injury (5 point categorical scale), patients/physician satisfaction assessment (10 point categorical scale), time to return to pain-free and disability-free sport and adverse events as per WHO definition. It is expected that the Hyaluronic acid injections will decrease pain and swelling, promote healing, improve time to return to sport and increase mobility.

NCT ID: NCT01987570 Completed - Clinical trials for Patients With Grade II Ankle Sprain

Effect of Allopurinol Administration on the Prevention of Muscle Mass Loss in Subject Immobilized.

Start date: April 2012
Phase: Phase 3
Study type: Interventional

Generating critical levels of power is a prerequisite for performing simple daily activities, such as rising from a chair or climbing stairs. For a young healthy person these activities can be performed easily, however after a prolonged period of forced inactivity (such as during the recovery from a sports injury, prolonged bed rest or spaceflight) a loss of muscle mass occurs. It has been suggested that this loss may be triggered by oxidative stress. An enzyme involved in the production of free radicals in various experimental models, including immobilization, is xanthine oxidase (XO). Although allopurinol is an inhibitor of XO widely used in clinical practice, its effect on the maintenance of muscle mass after an immobilization protocol is unknown. Thus, the major aim of this clinical trial is to determine the effect of allopurinol administration on the prevention of muscle mass loss in immobilized subjects. This is a prospective, randomized study in which fifty young male subjects (aged between 25 and 40 years) diagnosed with grade II ankle sprain will be recruited. After immobilization the patients will be assigned randomly to one of two experimental groups, one treated with allopurinol (n=25) and the other with placebo (n=25). The dosage of allopurinol will be the same as recommended for gout patients, i.e. 300 mg/day orally, during all the immobilization period, which will last fifteen days. This medication will be delivered to the patients when they agree to participate in the clinical trial. They will be immobilized by posterior knee splint, preventing use of that leg. We will determine muscle mass loss by performing two magnetic resonances of both legs before and after the immobilization period. We will also take two blood samples (before and after immobilization) to measure oxidative stress parameters (malondialdehyde, protein carbonyls, and XO activity), inflammatory parameters (IL-6, C-reactive protein and 1-antichymotrypsin), as well as vitamin D levels.

NCT ID: NCT01957215 Completed - Ankle Sprain Clinical Trials

Efficacy of Topical Indomethacin Patch Over Placebo in Ankle Sprain Pain Relief

Start date: October 2013
Phase: Phase 4
Study type: Interventional

This study will investigate the efficacy of the Indomethacin patch in pain relief of ankle sprain in adult patients, compared to a placebo patch

NCT ID: NCT01945034 Completed - Ankle Injuries Clinical Trials

5% Topical Ibuprofen (IBU) for Ankle Sprain

Start date: November 2013
Phase: Phase 3
Study type: Interventional

This study is being conducted to evaluate the effects of IBU 5% Topical Gel versus topical placebo for the relief of pain associated with a first or second degree ankle sprain. Both twice daily and three times daily regimens will be evaluated.