Clinical trials: Hallux Valgus Deformity
Medial Malleolus Fracture, Lisfranc Injury
Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF Investigation
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…
- Conditions
- Medial Malleolus Fracture, Lisfranc Injury, Lisfranc Fracture, Talus Fracture
- Trial name
- NCT05555459
- Testing
- Operation
- Where
- Finland
- Volunteers
- 125 people
- Sponsor
- Inion Oy
Hallux Valgus
Medial Forefoot Block for Analgesia After Foot Surgery
Forefoot surgery includes bunion surgery and similar reconstructive bone cutting surgery and is very painful. Local anaesthetic nerve blocks are used to provide pain relief after this work.
- Trial name
- NCT01445249
- Testing
- Landmark guided ankle block., PNS guided block.
- Where
- United Kingdom
- Volunteers
- 72 people
- Sponsor
- Hull University Teaching Hospitals NHS Trust
Hallux Valgus
Acute Effects of Prolonged Walking on Hallux Valgus
Hallux valgus is a progressive foot deformity characterized by lateral deviation of the great toe and medial displacement of the first metatarsal head.
- Trial name
- NCT07177768
- Testing
- Prolonged walking
- Where
- Turkey (Türkiye)
- Volunteers
- 32 people, healthy volunteers welcome
- Sponsor
- Bezmialem Vakif University
Hallux Valgus
Immediate Effect of Taping on Foot Biomechanics in Patients With Hallux Valgus
The goal of this clinical trial is to comparatively investigate the immediate effects of rigid taping and kinesiological taping applications on foot biomechanics in patients with hallux valgus (HV).
- Trial name
- Taping in HV (NCT07409974)
- Testing
- rigit taping, kinesiologic taping
- Where
- Turkey (Türkiye)
- Volunteers
- 30 people
- Sponsor
- Hacettepe University
Hyperpronated Foot, Reconstruction Surgeries of the Foot
Evaluate the Continued Safety and Performance of the Foot and Ankle Products
The objective of the registry is to evaluate the continued safety and performance of Arthrex foot and ankle products, including the ProStop® implant for hyperpronated foot; Bio-Compression Screw for reconstruction surgeries of…
- Conditions
- Hyperpronated Foot, Reconstruction Surgeries of the Foot, Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle, Fixation of Small Bone Fragments of the Foot/Ankle
- Trial name
- NCT04715139
- Testing
- Products listed in Group/Cohort Description
- Where
- 7 sites in United States, Germany and 1 more
- Volunteers
- 700 people, healthy volunteers welcome
- Sponsor
- Arthrex, Inc.
Pain
Efficacy and Safety Study of 4975 to Manage Pain of Bunionectomy
The primary purpose of this study is to compare the analgesic efficacy of a single intraoperative administration of 4975 vs. Placebo in the management of acute postoperative pain in patients undergoing bunionectomy.
- Trial name
- NCT00656578
- Testing
- 4975
- Where
- 6 sites in United States
- Volunteers
- 300 people
- Sponsor
- Anesiva, Inc.
Hallux Valgus, Hallux Limitus
The Hyalex MTP Study
The HYALEX SLALOM MTP Hemiarthroplasty System consists of a synthetic implant designed to replace the distal metatarsal surface of the great toe for treatment of arthritis .
- Conditions
- Hallux Valgus, Hallux Limitus, Hallux Rigidus
- Trial name
- NCT07538141
- Testing
- MTP Hemiarthroplasty
- Where
- Poland
- Volunteers
- 20 people
- Sponsor
- Hyalex Orthopaedics, Inc.
Hallux Valgus, Postoperative Pain
A Study Comparing Etoricoxib and Diclofenac Sodium in Post Hallux Valgus Surgery Pain
The investigators hypothesize that cyclooxygenas-II-selective inhibitors (Coxibs) provide a better patients assessed overall satisfaction when used for pain management after elective hallux valgus surgery as compared to…
- Trial name
- NCT01190722
- Testing
- etoricoxib, Diclofenac
- Sponsor
- Karolinska Institutet
Hallux Valgus
COSMIC Study - Comparing Open Scarf/Akin Osteotomy and Minimally Invasive Chevron/Akin. A Feasibility Study
The aim of this study is to assess the feasibility of conducting a study to compare the patient recorded and clinical outcomes for the surgical management of Hallux Valgus correction.
- Trial name
- NCT02915822
- Testing
- Minimally Invasive Chevron/Akin osteotomy, Open Scarf/Akin osteotomy
- Where
- United Kingdom
- Volunteers
- 43 people
- Sponsor
- Northumbria Healthcare NHS Foundation Trust
Hallux Valgus
Second Toe Length and Hallux Valgus: Greek vs. Egyptian Foot
A total of 150 patients aged 60-80 years with existing foot radiographs will be included in the study. Radiographic evaluations will include measurements of the hallux valgus angle, first intermetatarsal angle, and the metatarsal…
- Trial name
- NCT06874517
- Testing
- no intervention
- Where
- Turkey (Türkiye)
- Volunteers
- 150 people
- Sponsor
- Beylikduzu State Hospital
Hallux Valgus
Improving the Function of the Foot by Core Foot System (CFS) Exercise Theory in Patients After Hallux Valgus Surgical Procedure
The aim of the study is to identify the impact of CFS foot muscle training on time-space parameters, anthropometric parameters and bioelectrical activity (EMG) of the foot muscles during walking and to develop an algorithm for an…
- Trial name
- NCT05210127
- Testing
- Scarf osteotomy for Hallux Valgus deformity
- Volunteers
- 60 people
- Sponsor
- Józef Piłsudski University of Physical Education
Hallux Valgus
Chevron Osteotomy Versus SCARF Osteotomy in the Treatment of Hallux Valgus
Comparison between two techniques of osteotomy wich are more or less invasive : two criterias : clinical data and x-rays data. All patients operated for hallux valgus for 01/01/99 to 31/12/03 in the department of bone surgery CHU…
- Trial name
- NCT00455676
- Testing
- Chevron osteotomy versus Scarf osteotomy
- Where
- France
- Volunteers
- 74 people
- Sponsor
- University Hospital, Limoges
Rotator Cuff Repair, Anterior Cruciate Ligament Reconstruction
Ultrasound-Guided Percutaneous Peripheral Nerve Stimulation: A Department of Defense Funded Multicenter Pilot Study
Postoperative pain is usually treated with opioids that have undesirable and sometimes dangerous side effects (e.g., vomiting and respiratory depression)-and yet over 80% of patients still experience inadequate pain relief.
- Conditions
- Rotator Cuff Repair, Anterior Cruciate Ligament Reconstruction, Ankle Arthrodesis or Arthroplasty, Hallux Valgus Correction
- Trial name
- NCT03481725
- Testing
- ACTIVE peripheral nerve stimulation with a percutaneously inserted lead and wearable stimulator (SPR Therapeutics, Cleveland, Ohio)
- Where
- 6 sites in United States
- Volunteers
- 65 people
- Sponsor
- University of California, San Diego
Hallux Valgus and Bunion
Timing of Weight Bearing After Hallux Valgus Surgery
Investigate the optimal timing for weight bearing after Hallux Valgus surgery. Hypothesis: Early weight bearing does not affect outcome after the Endoscopic Distal Soft Tissue Procedure for Hallux Valgus Correction.
- Trial name
- NCT03340415
- Testing
- Accelerated Rehabilitation plan
- Where
- Hong Kong
- Volunteers
- 53 people
- Sponsor
- North District Hospital
Hallux Valgus
Prospective Trial of Minimally Invasive Surgery Versus Standard Surgery for Correction of Hallux Valgus
Hallux valgus is a common deformity of the big toe, defined as medial deviation of the first metatarsal bone along with lateral deviation of the first toe.
- Trial name
- Minibunion (NCT01602926)
- Testing
- conventional surgical technique - Chevron-type distal metatarsal osteotomy, minimally invasive surgical technique
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Henry DeGroot, M.D.
Hallux Valgus
Human Bone Graft for Hallux Valgus Correction According to the Austin Procedure
This observational study is to document the application of a human bone graft in the surgical repair of hallux valgus deformity and its subsequent healing process.
- Trial name
- NCT03884907
- Testing
- The patients will receive human bone graft screws surgically
- Where
- 2 sites in Austria
- Volunteers
- 50 people
- Sponsor
- Klinikum Wels-Grieskirchen
Hallux Valgus, Bunion
Early Weight-Bearing After the Lapiplasty Mini-Incision Procedure (Mini3D)
Prospective, multicenter, unblinded study to evaluate outcomes of the Lapiplasty® Procedure using the Lapiplasty® Mini-Incision™ System for patients in need of hallux valgus surgery.
- Trial name
- Mini3D (NCT05082012)
- Testing
- Treatment of Hallux Valgus
- Where
- 10 sites in United States
- Volunteers
- 123 people, healthy volunteers welcome
- Sponsor
- Treace Medical Concepts, Inc.
Hallux Valgus and Bunion
Proximal Metatarsal Osteotomy in Correction of Hallux Valgus
The outcomes of the correction of hallux valgus by proximal opening wedge osteotomy
- Trial name
- NCT06584487
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- Assiut University
Hallux Valgus
Functional and Radiographic Outcomes of Hallux Valgus Correction by Mini-invasive Surgery With Reverdin-Isham Percutaneous Osteotomy
Minimally invasive surgery (MIS) represents one of the most innovative surgical treatments of Hallux Valgus (HV). However, long-term outcomes still remain a matter of discussion within the orthopaedic community.
- Trial name
- MISHV (NCT02886221)
- Where
- Italy
- Volunteers
- 250 people
- Sponsor
- University of Padova
Hallux Valgus, Surgery
Assessment of the Ionizing Radiation Received During Percutaneous or Conventional Surgery of Hallux Valgus
To assess the average whole body radiation dose received by the surgeon, the operating team and the patient during hallux valgus surgery, depending on whether the surgery is percutaneous or conventional.
- Trial name
- RADUS (NCT05174702)
- Testing
- Irradiation collected at the end of the operation on the active dosimeter
- Where
- France
- Volunteers
- 71 people
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche