Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Ankle Injuries and Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 15
- Active, not recruiting: 4
- Completed: 23
- Other: 8
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT04800484 — The Effects of AFO Heel Height and Stiffness on Gait
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Iowa |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Musculoskeletal Injury; Musculoskeletal Diseases; Peripheral Nervous System Diseases |
| Interventions | ; ; |
The proposed study evaluates the effect of ankle foot orthosis (AFO) heel height and stiffness on the forces and motion of the lower limb during over-ground walking in individuals who use an AFO for daily walking. Previous studies suggest that heel height and stiffness effect limb loading, but these data and the analysis techniques applied are limited. In this study, heel cushions with differen…
NCT03663361 — Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Phillip Gribble |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Sprains |
| Interventions | ; |
The purpose of this project is to compare a novel sensorimotor ankle rehabilitation training (SMART) protocol for Lateral ankle sprains (LASs) against a standard of care (SOC) protocol to determine if it is more successful at producing successful one-year outcomes and lower rates of re-injury and improved health. This will address the identified needs for evidence-support and reintegration stra…
NCT05196906 — The Clinical Outcomes of the Modified Broström vs Anatomic Reconstruction Operation in CLAI and GJL
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Peking University Third Hospital |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Sprains; Instability, Joint; Joint Hypermobility |
| Interventions |
Investigators designed this prospective cohort study to compare the clinical outcomes of modified Broström operation and anatomical reconstruction for the treatment of CLAI and GJL.
NCT06897293 — Comparison of MBR + Suture Tape and MBR for CLAI : A Prospective Cohort Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Peking University Third Hospital |
| Enrollment | 86 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Sprain; Hypermobility, Joint |
| Interventions | ; |
GJL is a risk factor for postoperative recurrent instability following an MBR for CLAI. Additional suture tape augmentation has been suggested to provide more strength and stability. However, the outcomes of the MBP with suture tape augmentation were unknown, which requires further exploration.
NCT05555459 — Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF Investigation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Inion Oy |
| Enrollment | 125 |
| Study Type | INTERVENTIONAL |
| Conditions | Medial Malleolus Fracture; Lisfranc Injury; Lisfranc Fracture; Talus Fracture; Calcaneus Fracture |
| Interventions |
The study in question is a post market clinical follow up (PMCF) study to evaluate the safety and performance of bioabsorbable headless compression screw Inion CompressOn in selected fracture, osteotomy and arthrodeses operations of the foot and ankle. The study recruits 125 adult patients who meet the acceptance criteria. The follow-up time for each study patient is 4 years. The study is a sin…
NCT07090057 — The Effect of Targeting the Plantaris Muscle-tendon in Surgical Correction of Ankle Equinus in Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alberta |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Idiopathic Toe Walking; Cerebral Palsy; Hereditary Spastic Paraparesis; Traumatic Brain Injury; Spinal Cord Injury |
| Interventions | ; |
Tight ankle muscles can produce ankle equinus (limited ability to pull the foot upward) and occur often in children, significantly impacting their ability to walk. If not treated, children with ankle equinus frequently experience reduced function and long-term foot problems, such as pain. Currently, treatment options include surgery or Botulinum toxin (BoNTA) injection into the large calf muscl…
NCT05644522 — Nomad P-KAFO Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Shirley Ryan AbilityLab |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Cerebrovascular Accident; Post-polio Syndrome; Spinal Cord Injuries; Multiple Sclerosis; Muscular Dystrophy |
| Interventions |
The goal of this clinical trial is to evaluate the impact of using the Nomad powered KAFO in people who have had a musculoskeletal or neurological injury that has affected their ability to walk. The main questions it aims to answer are to quantify the effectiveness of the Nomad in improving mobility, balance, frequency of falls, and quality of life in individuals with lower-extremity impairment…
NCT06898554 — Spinal and Supraspinal Control in Chronic Ankle Instability
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ayca Yagcioglu |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Injuries; Ankle Sprains |
| Interventions |
Ankle sprains are common sports injuries that often lead to chronic ankle instability (CAI). Patients with CAI experience deficits in neuromuscular control (NMC), including proprioception and strength. It is believed that damage to the ankle’s ligament mechanoreceptors and the peroneal nerve after the initial ankle sprain can cause alterations in NMC, resulting in postural control and dynamic j…
NCT06780202 — Assessment of Medrol Dosepak to Reduce Opioid Consumption in Foot and Ankle Surgical Patients
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Emory University |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Foot Injuries and Disorders; Ankle Injuries and Disorders; Achilles Tendon Injury |
| Interventions | ; |
This clinical trial aims to determine the effects of a 6-day low-dose methylprednisolone course on pain, nausea, and total opioid consumption in patients undergoing foot and ankle surgeries.
The secondary objective of the study is to determine and monitor the effects of the course on complications following surgery and patient-reported outcomes
NCT07054892 — Assessment of the Quality of Life of Patients Visiting the Emergency Department of the Saint-Brieuc Hospital Following an Ankle Sprain
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier de Saint-Brieuc |
| Enrollment | 176 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Injuries; Treatment Outcome |
| Interventions |
Lateral ankle sprains account for nearly 6,500 emergency department visits per day in France. They are clinically classified into three grades, which can be assessed approximately 3-5 days after an acute sprain. However, this classification remains somewhat approximate, with only mild and severe sprains being reliably identified.
When it comes to immobilization, if weight-bearing is possible, …
NCT06949826 — Buprenorphine as a Post-operative Analgesic in Opioid-Naive Patients After Ankle Fracture Surgery
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Jenna-Leigh Wilson |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain, Postoperative; Ankle Fracture Surgery; Opioid Use Disorder; Opioid Dependence; Opioid Analgesia |
| Interventions | ; |
Addictive full-agonist opioids, like oxycodone and hydrocodone, are often used to treat pain after surgery. However, these full-agonist opioids can be very addictive. After ankle fracture surgery, about 1 in 5 patients that did not take opioids before surgery become addicted to opioids after surgery. Buprenorphine is an opioid with unique properties that may offer a way to reduce the number of …
NCT06868316 — Auditory Biofeedback Gait Training Individuals With Chronic Ankle Instability
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Kentucky |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Sprains; Ankle Injuries and Disorders |
| Interventions | ; ; |
The goal of this randomized clinical controlled trial is examine the effects of gait training with auditory biofeedback (AudFB) on gait biomechanics, clinical measures of ankle joint health, and patient-centered outcomes. The following specific aims will achieve this objective:
- Specific Aim 1: Determine if a 6-week gait training with AudFB intervention improves lower extremity biomechanics c…
NCT06828653 — Comparing Digitally and Traditionally Made Ankle Foot Orthoses
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Holland Bloorview Kids Rehabilitation Hospital |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Flaccid Paresis; Spastic Paresis; Cerebral Palsy; Stroke; Spinal Cord Injury |
| Interventions | ; ; |
The research is being done to compare two methods of creating AFOs: 1. The traditional method, which involves manually creating a mold from a plaster cast of the client’s limb. This is time-consuming and labor-intensive; and 2. The newer method uses digital technology, such as 3D scanning and printing, to design and produce the AFOs, potentially making the process faster and less costly. We wan…
NCT07231471 — Platelet Rich Plasma for Musculoskeletal Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Utah |
| Enrollment | 10000 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis (OA); Osteoarthritis (OA) of the Knee; Osteoarthritis (OA) of the Hip; Osteoarthritis (OA) of the Shoulder; Osteoarthritis Ankle |
| Interventions | ; |
The primary purpose of this study is to follow patients with various musculoskeletal (MSK) conditions over a one-year follow-up period after receiving a platelet rich plasma (PRP) injection, assessing changes in their pain levels, functional abilities, and overall patient satisfaction.
This will develop a robust registry of patients treated with PRP for a range of MSK conditions. These conditi…
NCT07335133 — Postoperative Complications of Ankle Arthroscopy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Clinique Saint Jean, France |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Injuries and Disorders; Surgery Complications |
| Interventions |
The goal of this clinical trial is to describe complications that occurred in the year following surgery, based on follow-up surgical consultations and physical therapy sessions.
The target population is any adult patient who has undergone ankle surgery performed under arthroscopy.
Primary outcome is description of all complications occurring within one year following ankle arthroscopy. This …
Active, Not Recruiting
NCT02089880 — Comparing Functional Outcomes in Individuals Using Micro-processor Controlled Orthosis Versus Stance Control Orthosis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Shirley Ryan AbilityLab |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injuries; Poliomyelitis; Post-polio Syndrome; Arthritis; Lower Motor Neurone Lesion |
| Interventions | ; |
The study will specifically evaluate the potential of the C-Brace to improve the functional mobility and quality of life in individuals with lower extremity impairments due to neurologic or neuromuscular disease, orthopedic disease or trauma, as compared to the stance control orthosis.
NCT03930056 — C-Brace II Spinal Cord Injury
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Shirley Ryan AbilityLab |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury |
| Interventions | ; |
A randomized, repeated measures comparative design study to compare use of a micro-processor controlled knee-ankle-foot orthosis vs. traditional care knee-ankle-foot-orthosis (KAFO) models following discharge from inpatient rehabilitation.
NCT05915065 — VR to Evaluate Phantom Limb Pain
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Shirley Ryan AbilityLab |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Phantom Limb Pain; Phantom Pain; Phantom Sensation; Phantom Limb Syndrome With Pain; Phantom Pain Following Amputation of Lower Limb |
| Interventions |
The objective of this study is to develop a virtual rehabilitation system that can be used to effectively treat Phantom Limb Pain (PLP) within the research setting and for at-home use by individuals with upper and lower extremity amputation.
We hypothesize that the system will improve PLP for individuals with upper or lower extremity amputation, as measured through with various outcome measure…
NCT04944576 — Observational Study to Evaluate Safety and Performance of the Total Ankle Prosthesis, EasyMove®
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | FH ORTHO |
| Enrollment | 82 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Injuries and Disorders |
| Interventions |
This study is a post-market clinical follow-up conducted in order to collect long-term data on safety and performance of the EasyMove prosthesis, which is intended to be implanted in case of total ankle replacement, when used in real life conditions according to the instructions for use.
Not Yet Recruiting
NCT07460310 — Comparison of Anesthetic Techniques for Early Recovery After Ankle Arthroscopy
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Sprain; Ankle (Ligaments); Instability (Old Injury); Pain Management; ERAS; Ankle Arthroscopy |
| Interventions | ; ; |
Ankle arthroscopy is increasingly performed as a day-case procedure, making rapid recovery and efficient discharge critical. Anesthetic technique substantially influences postoperative recovery, yet high-quality evidence comparing anesthetic strategies in ankle arthroscopy is limited.
This multicenter randomized trial compares total intravenous anesthesia with propofol plus peripheral nerve bl…
NCT07508163 — Distinct Directional Postural Stability Deficits Across Lower Limb Musculoskeletal Disorders
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 90 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Sprains; Patellofemoral Pain Syndrome |
| Interventions |
Lateral ankle sprain (LAS) and patellofemoral pain syndrome (PFPS) are common musculoskeletal conditions associated with postural instability. However, the direction-specific nature of balance deficits and comparative patterns across these conditions remain unclear. Therefore, the aim of this study is to compare overall, mediolateral, and anteroposterior postural stability indices among individ…
Enrolling by Invitation
NCT02664337 — Conjoint Analysis of Patient Preferences in Joint Interventions
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 2310 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis; Femoroacetabular Impingement; Osteochondritis Dissecans; Hip Fractures; Ankle Fractures |
| Interventions | ; |
This study is an observational study to test and validate a questionnaire and statistical model used to determine patient preferences regarding treatment for any one of 11 musculoskeletal conditions: hip arthritis, knee arthritis, hip labral tears and femoroacetabular impingement (FAI), osteochondritis dissecans, Achilles tendon rupture, patellofemoral dislocation, distal radius fracture, and f…
NCT07052721 — Randomized Study of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot Surgery
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Rotator Cuff Tears; Shoulder Injuries; Hallux Valgus; Ankle Arthropathy; Clavicle Fracture |
| Interventions | ; |
Postoperative pain remains undertreated with inadequate analgesic options. Opioids have well-known limitations for both individuals and society; single-injection and continuous peripheral nerve blocks provide intense analgesia but are limited in duration to 24-72 hours; and current neuromodulation options-with a duration measured in weeks and not hours-are prohibitively expensive and require an…
Completed Trials
NCT01961557 — Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Incomplete Spinal Cord Injury; Muscular Dystrophy; Spina Bifida; Cerebral Palsy |
| Interventions |
Background:
- Cerebral palsy (CP) is the most common motor disorder in children. CP often causes crouch gait, an abnormal way of walking. Knee crouch has many causes, so no single device or approach works best for everybody. This study s adjustable brace provides many types of walking assistance. Researchers will evaluate brace options to find the best solution for each participant, and wheth…
NCT03809520 — An Imaging Framework for Clinically Testing New Treatments to Prevent Post-traumatic OA
| Status | Completed |
| Phase | N/A |
| Sponsor | J L Marsh |
| Enrollment | 97 |
| Study Type | INTERVENTIONAL |
| Conditions | Orthopedic Disorder; Trauma; Ankle Fractures; Post-traumatic Osteoarthritis |
| Interventions |
The immediate goal of the proposed research is to test the value of a new low-cost, low-dose standing CT system for efficient early detection of both joint degeneration and elevated contact stress. The standing CT scanner holds promise for detecting arthritic changes earlier than other imaging modalities because of the combination of its 3D nature and ability to image joints in a weight-bearing…
NCT04562896 — Iterative Design of Custom Dynamic Orthoses to Reduce Articular Contact Stress
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Iowa |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Fractures; Post-traumatic Osteoarthritis; Osteoarthritis Ankle |
| Interventions |
The proposed study evaluates the effect of carbon fiber brace design on forces across the ankle joint. Research suggests that ankle arthritis develops after ankle fracture, in part, due to elevated forces on the cartilage. It is expected that carbon fiber braces can be designed to reduce forces in the ankle joint and thereby reduce the risk of developing arthritis following traumatic injury. In…
NCT03901053 — Ankle Foot Orthosis Comparative Effect
| Status | Completed |
| Phase | N/A |
| Sponsor | Jason Wilken |
| Enrollment | 54 |
| Study Type | INTERVENTIONAL |
| Conditions | Foot Injuries and Disorders |
| Interventions | ; |
The proposed effort is designed to support evidence-based practice and optimal care by evaluating how the form, fit and function of two commercially available carbon fiber custom fit braces (Orthoses) influences outcomes following extremity injury. Early data suggests that custom fit carbon fiber braces can significantly improve function following severe lower leg injuries. The proposed study w…
NCT04229563 — Post-Market Registry of AURYON Atherectomy Device in Subjects Affected With Infrainguinal Peripheral Artery Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Angiodynamics, Inc. |
| Enrollment | 102 |
| Study Type | OBSERVATIONAL |
| Conditions | Infrainguinal Peripheral Artery Disease; Peripheral Arterial Disease; PAD |
| Interventions |
The PATHFINDER Registry is a prospective, non-randomized, single arm, multicenter observational study. This pilot registry is aimed to evaluate the performance (peri-procedural) and clinical outcomes (intermediate and long-term) of the AURYON Atherectomy System, within the initial launch phase of the product in the market.
NCT06930963 — Impact of AFOs on the GMF of Children With CP or ABI
| Status | Completed |
| Phase | N/A |
| Sponsor | Universitaire Ziekenhuizen KU Leuven |
| Enrollment | 29 |
| Study Type | OBSERVATIONAL |
| Conditions | Spastic Cerebral Palsy (sCP); Acquired Brain Injury |
Children with cerebral palsy (CP) or an acquired brain injury (ABI) are often prescribed ankle-foot orthoses (AFOs) to correct impairments of muscles and/or to prevent contractures and bony deformities. The impact of AFOs on gait, and to a lesser extent on gross motor function (GMF), has been investigated. Yet, little is known about their impact on the quality of movement. This study aims to ex…
NCT05662449 — A Cohort Study of Bioabsorbable Screws for Syndesmosis Fixation Fixation in Ankle Fracture
| Status | Completed |
| Phase | N/A |
| Sponsor | NHS Grampian |
| Enrollment | 15 |
| Study Type | OBSERVATIONAL |
| Conditions | Syndesmotic Injuries; Ankle Fractures; Ankle Injuries and Disorders |
| Interventions |
The investigators aim to evaluate the fixation of the ankle syndesmosis in appropriate ankle fractures with bioabsorbable screws.
Ankle fractures are common, and a proportion of them involve both fracture of the bone and also disruption of the syndesmosis, a strong ligamentous complex connecting the distal fibula and tibia. If left without fixation this causes a high incidence of pain and earl…
NCT04390048 — Balance Training With tDCS for CAI
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Miami |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Injuries and Disorders |
| Interventions | ; |
The purpose of this research study is to examine the efficacy of non-invasive brain stimulation in addition to balance exercise for chronic ankle instability (CAI), a condition that develops following an initial ankle sprain, usually because of loose or unstable ankle joints.
NCT05112679 — Limb Health and Socket Pressure in Response to Powered Ankle Protheses
| Status | Completed |
| Phase | N/A |
| Sponsor | Indiana University |
| Enrollment | 6 |
| Study Type | INTERVENTIONAL |
| Conditions | Pressure Ulcer, Ankle; Prosthesis User; Prosthesis Durability; Mobility Limitation; Skin Wound |
| Interventions |
this project seeks to understand and quantify the effects of powered transtibial prostheses on socket loading and direct measures of residual limb health so as to inform the optimization of prosthesis fit.
NCT05494645 — Exparel Use in Peripheral Nerve Blocks and Local Infiltration for Foot and Ankle Surgery
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | St. Luke’s Hospital, Pennsylvania |
| Enrollment | 248 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain, Postoperative; Pain, Acute Postoperative; Ankle Fractures; Ankle Injuries and Disorders |
| Interventions | ; |
Liposomal Bupivacaine (Exparel) has been recently studied as the active agent utilized in various nerve block. Due to its liposomal form allowing for extended delivery, Exparel has been used in various peri-operative nerve blocks among multiple orthopaedic specialties in hopes of achieving improved pain control and decreased opioid use. This study compares the efficacy and effect on opioid use …
NCT05444192 — Comparing Clinical Outcomes Using Two Insole Manufacture Techniques
| Status | Completed |
| Phase | N/A |
| Sponsor | NHS Greater Glasgow and Clyde |
| Enrollment | 114 |
| Study Type | INTERVENTIONAL |
| Conditions | Foot Injury; Foot Deformity; Foot Sprain; Feet, Flat; Foot Ankle Injuries |
| Interventions |
The main purpose of this study is to find out if scanning the foot using a 3D scanner influences the effectiveness of custom made insoles, compared to the more traditional approach of taking a foam-box impression cast of the foot. Both of these methods are currently used as standard care in the NHS Greater Glasgow and Clyde (GGC) Orthotic Department. In this study, insoles will be manufactured …
NCT05456295 — Comparative Effect of Carbon Fiber Orthosis Cuff Design on Preference, Comfort, and Mechanics
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Iowa |
| Enrollment | 35 |
| Study Type | INTERVENTIONAL |
| Conditions | Healthy; Lower Limb Injury; Post-Traumatic Osteoarthritis |
| Interventions |
Carbon fiber custom dynamic orthoses (CDOs) consist of a proximal cuff that wraps around the leg just below the knee, a posterior carbon fiber strut that stores and returns energy during gait, and a carbon fiber foot plate that supports the foot and allows bending of the posterior strut. The proximal cuff is a primary interface between the patient and the CDO and may influence comfort, preferen…
NCT05942417 — Echoguided Percutaneous Neuromodulation in the Management of Chronic Ankle Instability in Physically Active Subjects.
| Status | Completed |
| Phase | N/A |
| Sponsor | Escoles Universitaries Gimbernat |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Transcutaneous Electric Nerve Stimulation; Ankle Injuries and Disorders : Chronic Ankle Instability; Exercise Therapy |
| Interventions | ; |
The lateral ankle complex sprain is the most prevalent musculoskeletal injury among the general population and athletes and is associated with long-term pain, disability, and high healthcare costs. One of the complications of a lateral ankle sprain is the development of chronic ankle instability (CAI). Conservative treatment is the initial therapeutic option for patients with CAI, however, the …
NCT06864312 — Rebound Pain Following Regional Anaesthesia for Ankle Fracture Surgery
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | University College Cork |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Fracture (bimalleolar Equivalent, Bimalleolar, or Trimalleolar); Ankle Fracture - Lateral Malleolus; Ankle Fracture - Medial Malleolus; Rebound Pain |
| Interventions | ; |
Regional anaesthesia is a commonly used and effective analgesic modality in orthopaedic surgery. The benefits of peripheral nerve blocks (PNB) include better pain relief, limited opioid consumption and high patient satisfaction(1-3).
Following ankle fracture surgery, rebound pain has been reported. The rebound effect was demonstrated in a randomised control trial comparing pain after ankle fra…
NCT06086418 — Perineural Dexamethasone on the Duration of Popliteal Nerve Block for Anesthesia After Pediatric Ankle Surgery
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Poznan University of Medical Sciences |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Disease; Ankle Injuries; Foot Injury; Foot Diseases |
| Interventions | ; ; |
Effect of Perineural Dexamethasone on the duration of popliteal nerve block for Anesthesia After Pediatric ankle/foot surgery.
NCT06134856 — A Study Examining Changes in Pain After Manual Therapy in People With Achilles Tendon Pain
| Status | Completed |
| Phase | N/A |
| Sponsor | Philadelphia College of Osteopathic Medicine |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Achilles Tendinopathy; Ankle Strain; Achilles Tendon Pain; Achilles Tendonitis |
| Interventions | ; |
The purpose of this research is to find out how pain sensation may change in the Achilles tendon after the use of manual physical therapy. The testing itself will use a device that gradually produces a sensation of heat or cold on your skin, which we will place directly over your Achilles Tendon. You will let the researcher know when the heat or cold becomes what you would describe as “slight d…
NCT06233565 — Dexamethasone vs. Dexmedetomidine for Popliteal Nerve Block in Pain Management After Pediatric Ankle and Foot Surgery
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Poznan University of Medical Sciences |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Foot Injuries and Disorders; Ankle Injuries and Disorders |
| Interventions | ; ; |
Effect of perineurial dexamethasone and dexmedetomidine on popliteal nerve block duration for pediatric, ankle or foot surgery
NCT06657937 — Evaluation of the Recovery Experienced by Patients After an Ankle Sprain Treated in the Emergency Department of Nantes University Hospital
| Status | Completed |
| Phase | N/A |
| Sponsor | Nantes University Hospital |
| Enrollment | 101 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Sprains |
| Interventions |
To evaluate the recovery experienced by patients with ankle sprains treated in the adult emergency department of Nantes University Hospital.
NCT06818708 — Feasibility of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot Surgery
| Status | Completed |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Rotator Cuff Injuries; Shoulder Disease; Hallux Valgus; Ankle Arthropathy |
| Interventions |
Postoperative pain remains undertreated with inadequate analgesic options. Opioids have well-known limitations for both individuals and society; single-injection and continuous peripheral nerve blocks provide intense analgesia but are limited in duration to 24-72 hours; and current neuromodulation options-with a duration measured in weeks and not hours-are prohibitively expensive and require an…
NCT06959472 — Impact of Hyperarch Fascia Training on Ankle Health and Exercise Performance
| Status | Completed |
| Phase | N/A |
| Sponsor | Applied Science & Performance Institute |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Injuries; Sprains and Strains; Joint Instability |
| Interventions |
The purpose of this clinical trial is to evaluate whether the Hyperarch Fascia Training (HFT) program can reduce ankle pain and improve jump performance in active adults aged 20-45 with a history of ankle sprains. Participants will be randomly assigned to either an HFT intervention group or a control group, maintaining regular activity. Over 12 weeks, participants will complete remote training …
NCT07328022 — Efficacy and Safety of Etoricoxib/Betamethasone Combination in Acute Bursitis, Tendinitis and Synovitis
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Laboratorios Silanes S.A. de C.V. |
| Enrollment | 89 |
| Study Type | INTERVENTIONAL |
| Conditions | Bursitis; Tendinitis; Synovitis |
| Interventions | ; |
Phase III, multicenter, prospective, randomized, double-blind, parallel-group study to evaluate the efficacy and safety of a fixed-dose combination of etoricoxib/betamethasone compared with etoricoxib alone in patients with an acute episode of bursitis, tendinitis, or synovitis affecting the shoulder, elbow, knee, or ankle.
NCT07344493 — Average ANKLE GO Score in the Objective Functional Assessment of the Ankle in Healthy Military Personnel (ANKMIL)
| Status | Completed |
| Phase | N/A |
| Sponsor | Direction Centrale du Service de Santé des Armées |
| Enrollment | 96 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankle Disorders Injuries |
This research aims to establish reference values for the Ankle-Go score, a validated tool for functional assessment of the ankle, in healthy military personnel. The Ankle-Go score, already used in the civilian population after sprains or surgery, combines physical tests and subjective questionnaires to assess functional recovery of the ankle. No normative data currently exist for the military p…
NCT07475663 — Counterpain PXM Versus Diclofenac Versus Piroxicam
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Taisho Pharmaceutical Indonesia |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Sprain; Back Pain; Osteoarthritis (OA) of the Knee; Tennis Elbow; Runner’s Knee |
| Interventions | ; ; |
The goal of this clinical trial is to learn if a gel containing Piroxicam plus Counterirritant (warming/cooling ingredients) is as effective and safe as two other common anti-inflammatory gels for treating acute muscle, bone, and joint pain in adults aged 18-60. The main questions it aims to answer are:
Does the Piroxicam plus Counterirritant gel provide a similar level of pain relief as the s…
Other (Terminated)
NCT03507972 — Evaluation of the Benefits of Ultrasound in Improving the Diagnosis and Management of Injuries the Child’s Ankle
| Status | Terminated |
| Phase | N/A |
| Sponsor | University Hospital, Lille |
| Enrollment | 97 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Trauma |
| Interventions | ; |
Evaluate ankle’s ultrasound contribution in the accuracy of ankle’s diagnosis of traumatic injuries (objectivated by reference’s examination : ankle’s MRI)
NCT05692401 — Weight Change With Controlled Ankle Movement (CAM) Boot Use
| Status | Terminated |
| Phase | N/A |
| Sponsor | Nell Blake, DPM |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Injuries; Foot Injuries and Disorders; Body Weight Changes |
| Interventions |
The purpose of the study is to determine if patients wearing a CAM boot have a change in weight compared to patients who wear a CAM boot and are provided nutritional guidelines and perform upper body exercises.
Other (Unknown)
NCT06304324 — Dexmedetomidine Vs Dexamethasone in Popliteal Nerve Block
| Status | Unknown |
| Phase | Phase 4 |
| Sponsor | Poznan University of Medical Sciences |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Disease; Ankle Injuries and Disorders; Foot Injury; Foot Diseases |
| Interventions | ; ; |
Effect of Perineural Dexmedetomidine vs. Dexamethasone on the duration of popliteal nerve block for Anesthesia After Pediatric ankle/foot surgery.
Other (Withdrawn)
NCT05209347 — Custom Dynamic Orthoses to Reduce Articular Contact Stress
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | University of Iowa |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Ankle Fractures; Post-traumatic Osteoarthritis; Osteoarthritis Ankle |
| Interventions |
The proposed study evaluates the effect of carbon fiber brace design on forces across the ankle. Research suggests that ankle arthritis develops following ankle fracture due, in part, to elevated forces on the cartilage. It is expected that carbon fiber braces can reduce forces in the ankle joint thereby reducing the risk of developing arthritis following injury. In this study, carbon fiber bra…