[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"foot-deformities\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:foot-deformities":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,37,68,128,161],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":4},"100639393","prevalence-of-foot-deformities-among-adolescents-in-egyptian-population-100639393",false,"NCT07627659","Prevalence of Foot Deformities Among Adolescents in Egyptian Population","Inclusion Criteria:\n\n* Adolescents aged 12-18 years.\n* Willingness to participate and provide informed consent (from both the participant and guardian).\n* Ability to stand and walk without assistance for the physical examination.\n\nExclusion Criteria:\n\n* Adolescents with a history of major lower limb surgery or amputation.\n* Those with severe neurological disorders affecting gait or foot structure (e.g., cerebral palsy, spina bifida).\n* Individuals unable to cooperate with the examination due to cognitive or psychiatric disorders.\n* Presence of acute foot trauma or infection at the time of assessment.","ALL","12 Years","18 Years",{"count":19,"type":20},4000,"ESTIMATED","OBSERVATIONAL","The aim of the study is to determine the prevalence of foot deformities among adolescents and associated factors such as age, sex, and pain. This includes identifying the types and degrees of deformities present, assessing their impact on adolescents' health, and examining how these deformities may influence daily activities",[24],"Foot Deformities","NOT_YET_RECRUITING","2026-05-31",{"date":28,"type":29},"2026-06-04","ACTUAL",{"date":31,"type":20},"2027-04",{"date":33,"type":20},"2028-12",{"name":35,"class":36},"Assiut University","OTHER",{"id":38,"slug":39,"hasResults":11,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":43,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":15,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":50,"conditions":51,"keywords":53,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":4},"100640962","translation-cross-cultural-adaptation-and-validation-of-the-fpi-6-in-spain-100640962","NCT07590297","Translation, Cross-cultural Adaptation, and Validation of the FPI-6 in Spain","Translation, Cross-cultural Adaptation, and Validation of the Foot Posture Index (FPI-6) in Spain","FPI-6-ES","Inclusion Criteria:\n\n* Participants aged between 6 and 89 years\n* Ability to understand and sign the informed consent form. In the case of minors, written informed consent from parents or legal guardians and child's assent (where applicable) are required\n* Ability to maintain a relaxed standing position unassisted for the duration of the clinical assessment\n\nExclusion Criteria:\n\n* History of major surgery or significant trauma in the lower limbs or feet.\n* Presence of open wounds or active skin infections on the feet at the time of the examination.\n* Neurological or musculoskeletal conditions that severely affect balance or standing posture.\n* Cognitive impairment that prevents the participant from following simple clinical instructions",true,"6 Years","89 Years",{"count":49,"type":20},100,"The objective of this study is to translate, cross-culturally adapt, and validate the Spanish version of the Foot Posture Index (FPI-6). This clinical tool is widely used to evaluate standing foot posture through six visual criteria. The study aims to provide Spanish-speaking clinicians and researchers with a reliable and valid instrument to assess foot posture in the Spanish population, ensuring that the psychometric properties of the original scale are preserved",[24,52],"Flatfoot",[54,55,56,57,58],"Foot Posture Index","FPI-6","Validation Study","Reliability","Spanish Version","2026-05-09",{"date":61,"type":29},"2026-05-15",{"date":63,"type":20},"2026-05-16",{"date":65,"type":20},"2028-05",{"name":67,"class":36},"Paloma López Ros",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":15,"minAge":17,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":100,"overallStatus":116,"whyStopped":4,"lastUpdateSubmitDate":117,"lastUpdatePostDateStruct":118,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":127},"100481933","performance-and-safety-evaluation-of-inion-compresson-screw-in-foot-and-ankle-surgeries-pmcf-investigation-100481933","NCT05555459","Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF Investigation","The Performance and Safety Evaluation of Bioabsorbable Headless Inion CompressOn Screws in Selected Fracture, Osteotomy and Artrodesis Surgeries of the Foot and Ankle","Inclusion Criteria:\n\n1. Read the patient information bulletin on the study and signed the patient consent form\n2. Adult patient (over 18-year-old)\n3. Suitable and in need for surgical lower limb operation listed in the indications of this study that requires fastening of bone structures with screws (or an alternative attachment method) in the ankle or foot area, according to a statement of the investigator surgeon\n4. Ability to fill in questionnaires.\n5. Willingness to comply with rehabilitation instructions.\n6. Availability for follow-up visits.\n\nExclusion Criteria:\n\n1. Active infection\n2. Patient conditions including limited blood supply (e.g. patients with severe circulatory disorder of the lower limb\n3. Patient conditions including insufficient quality or quantity of bone (diagnosed osteoporosis, conditions causing secondary osteoporosis e.g. diabetes, rheumatism, eating disorder)\n4. Patient conditions where patient cooperation cannot be guaranteed (alcohol use, drug abuse etc.)\n5. High-load bearing indications (e.g., diaphyseal fractures of long bones) unless used in conjunction with traditional rigid fixation\n6. Patients with significant neuropathy\n7. Pregnancy\n8. Patients who refuse to participate\n9. Lower limb tumor or metastasis\n10. Complex Regional Pain Syndrome (CRPS) in operated foot",{"count":76,"type":20},125,"INTERVENTIONAL",[79],"NA","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 single center single group study which is conducted in Tampere University Hospital (TAYS) in Finland. The main focus of the study in terms of performance is to evaluate the bone healing\u002Fossification of operated areas. The main focus of the study in terms of safety is to evaluate the occurrence of adverse events and required revision surgeries that are or might be related to the study device.",[82,83,84,85,86,87,88,89,90,91,92,24,93,94,95,96,97,98,99],"Medial Malleolus Fracture","Lisfranc Injury","Lisfranc Fracture","Talus Fracture","Calcaneus Fracture","Navicular Fracture","Deformity, Foot","Ankle Fractures","Foot Fracture","Fractures, Bone","Fracture of Foot","Foot Injury","Feet Deformity Tarsus","Metatarsalgia","Hallux Rigidus","Hallux Valgus","Deformity of Toe","Deformity of Foot",[101,102,103,104,105,106,107,108,109,110,111,112,113,114,115],"bioabsorbable screw","compression screw","headless screw","orthopaedic screw","bone fixation","bioabsorbable screw study","resorbable","biodegradable","bioabsorbable","fracture fixation with resorbable implants","inion","post-market follow-up study","orthopedic bone fixation","arthrodesis","osteotomy","RECRUITING","2026-03-11",{"date":119,"type":29},"2026-03-13",{"date":121,"type":29},"2023-03-07",{"date":123,"type":20},"2032-04-30",{"name":125,"class":126},"Inion Oy","INDUSTRY",1,{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":15,"minAge":17,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":77,"phases":138,"briefSummary":139,"conditions":140,"keywords":144,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":4},"100603448","custom-cadcam-insoles-for-plantar-pressure-improvement-in-foot-deformities-100603448","NCT07136649","Custom CAD\u002FCAM Insoles for Plantar Pressure Improvement in Foot Deformities","Effects of Custom CAD\u002FCAM Insoles on Plantar Pressure Distribution in Individuals With Foot Deformities: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18-65 years\n* Clinically diagnosed with a foot deformity (e.g., pes planus, pes cavus, hallux valgus)\n* Able to use custom insoles for at least six months\n* Able to stand and walk for pedobarographic measurements\n* Willing to participate and provide informed consent\n\nExclusion Criteria:\n\n* Presence of neurological or systemic diseases affecting foot function (e.g., diabetic neuropathy)\n* History of lower extremity surgery in the last six months\n* Severe musculoskeletal conditions impairing sensorimotor function\n* Any condition preventing compliance with insole use\n* Contraindications for participating in gait or pressure measurements","65 Years",{"count":137,"type":20},30,[79],"This randomized controlled trial will investigate the effects of custom CAD\u002FCAM insoles on plantar pressure distribution and gait parameters in individuals with foot deformities, such as pes planus, pes cavus, and hallux valgus. A total of 30 participants will be randomly assigned to either the intervention group, receiving custom CAD\u002FCAM insoles, or the control group, receiving no insole intervention.\n\nPlantar pressure measurements will be performed using the As200 Gait Scan Pedobarography System at baseline and after eight weeks. Static and dynamic plantar pressure variables, contact area, and center of pressure displacement will be assessed, along with gait parameters including step length, step time, and walking speed.\n\nThe results of this study may contribute to the development of effective conservative treatment strategies to improve foot biomechanics and reduce pressure-related complications in individuals with foot deformities.",[24,141,142,143],"Orthotic Device","3D Printing","CAD",[145,146,147,148,149,150,142,151],"Custom CAD\u002FCAM Insoles","Pes Planus","Pes Planovalgus","Pes Cavus","Pedobarography","Plantar Pressure","Orthotics","2025-08-21",{"date":154,"type":29},"2025-08-22",{"date":156,"type":20},"2025-09-01",{"date":158,"type":20},"2025-11-30",{"name":160,"class":36},"Fenerbahce University",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":165,"acronym":166,"eligibilityCriteria":167,"healthyVolunteers":45,"sex":15,"minAge":17,"maxAge":4,"enrollmentInfo":168,"targetDuration":4,"studyType":77,"phases":170,"briefSummary":171,"conditions":172,"keywords":176,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":127},"100596283","comparison-of-the-immediate-effects-of-mobilization-and-manipulation-versus-sham-manipulation-on-plantar-pressure-in-patients-with-hallux-valgus-100596283","NCT07043439","Comparison of the Immediate Effects of Mobilization and Manipulation Versus Sham Manipulation on Plantar Pressure in Patients With Hallux Valgus","HALLPRESS","Inclusion Criteria:\n\n* Be over 18 years of age\n* Volunteer to participate in the study\n* Have hallux valgus (those with a hallux valgus angle greater than 15 and a Manchester Scale score of B or higher)\n\nExclusion Criteria:\n\n* Having undergone surgery on the foot or ankle area within the last 6 months\n* Having any neurological or psychiatric problems",{"count":169,"type":20},60,[79],"The aim of this study is to examine the immediate effects of mobilization and manipulation versus sham manipulation on plantar pressure, quality of life, and pain in patients with hallux valgus. Participants will be assessed using a sociodemographic data form, the Manchester-Oxford Foot Questionnaire (MOXFQ), the Manchester Scale, goniometric measurements, the Multidimensional Nil Hallux Valgus Scale, the SF-36 Health Survey, the Numeric Pain Rating Scale (NPRS), and plantar pressure analysis via a pedobarographic device. The study will be conducted on a total of 60 feet, with 30 feet assigned to the manipulation group and 30 feet to the sham manipulation group.",[97,24,173,150,174,175],"Musculoskeletal Manipulations","Manuel Therapy","Chiropractic",[97,177,178,179,180,149,181,182,183,184],"First Metatarsal Mobilization","HVLA Manipulation","Sham Manipulation","Plantar Pressure Analysis","Manual Therapy","Chiropractic Mobilization","Pain","Quality of Life","2025-06-20",{"date":187,"type":29},"2025-06-29",{"date":189,"type":20},"2025-06-25",{"date":191,"type":20},"2025-08-25",{"name":193,"class":36},"SEFA HAKTAN HATIK"]