Hallux Valgus Clinical Trial
Official title:
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. A prospective trial will randomise the patients into two groups - Open Scarf/Akin osteotomy and Minimally Invasive Chevron/Akin osteotomy.
This study will assess the feasibility of a prospective trial that would randomise the patients into two groups for surgical correction of Hallux Valgus - Open Scarf/Akin osteotomy and Minimally Invasive Chevron/Akin osteotomy. Patients will complete a validated questionnaire (Manchester Oxford Foot questionnaire) preoperatively and post operatively at 6 months and 1 year. Range of motion of the Great Toe Metatarsal Phalangeal Joint will also be measured by goniometer. This study will assess the ability to recruit and retain patients and thus determine if a study comparing the surgical techniques would be feasible. In addition, for data collected statistical differences of the change in patient reported outcomes, range of motion between the two groups will be calculated with a significance level of p<0.05. This study will assess if a larger study comparing minimally invasive to open Hallux Valgus correction would be able to be performed ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
NCT04473196 -
The Effect of Weight Bearing on Patient Outcomes Following 1st MTP Joint Fusion
|
N/A | |
Recruiting |
NCT05587569 -
Outcomes Following Combined Adductoplasty™ and Lapiplasty® (MTA3D)
|
N/A | |
Recruiting |
NCT05555459 -
Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF Investigation
|
N/A | |
Completed |
NCT02121119 -
Lidocaine Versus Bupivacaine in Ambulatory Continuous Block With Elastomeric Pump
|
Phase 4 | |
Enrolling by invitation |
NCT00600899 -
Home Infusors for Analgesia After Foot Surgery
|
Phase 4 | |
Completed |
NCT05579054 -
Translation, Validity, and Reliability of the Foot Posture Index (FPI-6) - Turkish Version
|
||
Terminated |
NCT05082012 -
Early Weight-Bearing After the Lapiplasty Mini-Incision Procedure (Mini3D)
|
N/A | |
Recruiting |
NCT05051709 -
Can Hypermobility of First Ray Affect Surgical Treatment of Hallux Valgus
|
N/A | |
Recruiting |
NCT04716140 -
Prospective Study: The Effect on Clinical Outcome After Treatment of MTP Cartilage Lesions in Hallux Valgus Surgery
|
N/A | |
Active, not recruiting |
NCT04145882 -
Efficacy of Additional Osteotomies to Correct Hallux Valgus
|
N/A | |
Completed |
NCT04468555 -
Hallux Valgus Manual Therapy Based on Global Postural Reeducation.
|
N/A | |
Terminated |
NCT03257540 -
Early Weight-Bearing After Lapidus Arthrodesis
|
||
Completed |
NCT03846687 -
Validation of Patient Reported Outcome Measures for Use in Hallux Valgus
|
||
Completed |
NCT04365712 -
Osteotomy of the 1st Metatarsal for Hallux Valgus Using Pneumatic Oscillating Saw or Piezoelectric Scalpel
|
N/A | |
Recruiting |
NCT02282956 -
Ultrasound Guided Single Shot Block of Posterior Tibial Nerve for Postoperative Pain Relief After Hallux Valgus Surgery
|
Phase 4 | |
Withdrawn |
NCT01555216 -
Continuous Tibial Nerve Block Versus Single Shot Tibial Nerve Block
|
N/A | |
Completed |
NCT00683137 -
Analgesic Efficacy And Safety of Valdecoxib For Treatment Of Post-Surgical Pain From Bunionectomy Surgery
|
Phase 3 | |
Terminated |
NCT04103814 -
Effect of Topical CBD Cream for Degenerative Hallux Disorders
|
Phase 2/Phase 3 | |
Completed |
NCT03423498 -
The Toe-spread-out Exercise in Patients With Hallux Valgus and Without the Deformity
|
N/A | |
Not yet recruiting |
NCT06076655 -
Hallux Valgus Treatment Developed for Children With Cerebral Palsy
|
N/A |