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Bunion clinical trials

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NCT ID: NCT05602844 Active, not recruiting - Hallux Valgus Clinical Trials

Clinical Trial on Patient-Specific-Instrumentation Assisted Lapidus Fusion for Hallux Valgus

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

RCT to compare the effectiveness of PSI assisted Lapidus surgery vs conventional Lapidus surgery in hallux valgus.

NCT ID: NCT05587569 Recruiting - Hallux Valgus Clinical Trials

Outcomes Following Combined Adductoplasty™ and Lapiplasty® (MTA3D)

MTA3D
Start date: September 28, 2022
Phase: N/A
Study type: Interventional

Prospective, multicenter, unblinded study to evaluate outcomes of the Adductoplasty™ Procedure in combination with the Lapiplasty® Procedure for patients in need of metatarsus adductus and hallux valgus correction. Up to 80 subjects will be treated in this study at up to 13 clinical sites. Patients 14 years through 65 years with symptomatic metatarsus adductus and hallux valgus will be eligible to participate based on the inclusion and exclusion criteria defined in the study protocol.

NCT ID: NCT05408156 Not yet recruiting - Hallux Valgus Clinical Trials

Effects of Customized Insoles for Individuals With Symptomatic Hallux Valgus

Start date: August 1, 2024
Phase: N/A
Study type: Interventional

Hallux valgus is one of the most common forefoot deformities. Its prevalence increases with age, representing approximately 23% in adulthood, being more common in females. Some studies indicate that the use of the insole associated with the finger separator promotes pain relief and that this may be related to better alignment of the hallux. However, there is still no consensus about the ideal insole or how long it should be used to relieve pain or improve function in patients with hallux valgus. Therefore, the objective of this study will be to evaluate the effect of the customized insole on pain and function of individuals with symptomatic hallux valgus.

NCT ID: NCT05361317 Recruiting - Hallux Valgus Clinical Trials

Correction of Hallux Valgus With the Nexis® PECA Bunion Implantable Osteosynthesis Medical Device

PECA
Start date: June 13, 2022
Phase: N/A
Study type: Interventional

The Nexis® screw system is a range of osteosynthesis screws for the foot. Nexis® Bunion Screws are Class IIb implantable medical devices. The primary objective of the study is to confirm the performance and effectiveness of the device under investigation for the correction of hallux valgus with the evaluation functional capacities of the patient's foot. It will be assessed with "general sub-score" of the EFAS questionnaire determined during the postoperative visit at 6 months. The evaluation of quality of life scores, angular correction, bone consolidation and occurrence of adverse events will also be carried out.

NCT ID: NCT05344755 Completed - Pain Clinical Trials

Effects of Plantar Sensory Training in Individuals With Hallux Valgus.

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Hallux valgus is a forefoot deformity with a high prevalence, which can progress to lateral deviation of the big toe, medial deviation of the first metatarsal, and subluxation of the first metatarsophalangeal joint in the future. It has been reported in studies that changes in the load distribution of the foot in hallux valgus patients, hyperkeratosis, especially first-line pain, and sensory receptors on the sole of the foot may result in the effect of sensory receptors on the sole of the foot, and thus the balance may be negatively affected, poor postural stability and an increase in the risk of falling. It is thought that increased sensitivity to the senses coming from the feet with sensory training can improve the balance and reduce the risk of falling as a result of better perception of foot orientation and position.

NCT ID: NCT05210127 Not yet recruiting - Hallux Valgus Clinical Trials

Improving the Function of the Foot by Core Foot System (CFS) Exercise Theory in Patients After Hallux Valgus Surgical Procedure

Start date: June 1, 2022
Phase: Phase 1
Study type: Interventional

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 effective therapeutic method in patients after hallux valgus correction. Achieving the purpose of the research will contribute to the answer to the following research questions: - Does the CFS therapy used significantly change the arch of the foot in HV patients compared to the control group? - Does the CFS therapy used significantly improve gait characteristics after HV surgery in relation to the control group? - Does muscle stimulation and the moment of their activation differ in groups in which different therapies have been used? - Will the results of the questionnaires and scale be significantly different in both groups?

NCT ID: NCT05174702 Completed - Surgery Clinical Trials

Assessment of the Ionizing Radiation Received During Percutaneous or Conventional Surgery of Hallux Valgus

RADUS
Start date: January 5, 2022
Phase:
Study type: Observational

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.

NCT ID: NCT05165134 Completed - Hallux Valgus Clinical Trials

Hallux Valgus Conservative Treatment

RCT
Start date: August 24, 2020
Phase: N/A
Study type: Interventional

Studying the effect of kinesiotape on hallux valgus angle and pain in hallux valgus patients.

NCT ID: NCT05163431 Completed - Hallux Valgus Clinical Trials

Dimensional Validation of the Hallux Valgus Orthosis

Start date: July 20, 2021
Phase: N/A
Study type: Interventional

The goal of this project is to optimize the design of the orthosis by establishing the key volumetric characteristics of the custom iterations in order to subsequently transpose them to a standard model and establish the increment proportions of the different sizes. The final product should reduce the pain by repositioning the phalanges of the first toe with the first metatarsal in its axis.

NCT ID: NCT05082012 Active, not recruiting - Hallux Valgus Clinical Trials

Early Weight-Bearing After the Lapiplasty Mini-Incision Procedure (Mini3D)

Mini3D
Start date: September 17, 2021
Phase: N/A
Study type: Interventional

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. Up to 200 subjects will be treated in this study at up to 20 clinical sites. Patients 14 years through 58 years with symptomatic hallux valgus will be eligible to participate based on the inclusion and exclusion criteria defined in the study protocol.