Viewing Study NCT06562062



Ignite Creation Date: 2024-10-26 @ 3:38 PM
Last Modification Date: 2024-10-26 @ 3:38 PM
Study NCT ID: NCT06562062
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-16

Brief Title: Radiological Outcomes of Modified Extra-articular LCL
Sponsor: None
Organization: None

Study Overview

Official Title: Radiological Outcomes of Modified Extra-articular Lateral Column Lengthening Procedure for Correction of Adult Acquired Flexible Flatfoot Deformity
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To assess radiological and functional outcomes of modified extra-articular lateral column lengthening procedure for correction of adult acquired flexible flatfoot deformity
Detailed Description: Measurement of

1 Calcencal pitch This angle is formed on a weight-bearing lateral foot radiograph between the calcaneal Inclination axis and the supporting horizontal surface10 normal ranges of between 10-25 and 20-30 have Been proposed11
2 Mearys angle It is the angle between a line drawn along the longitudinal axis of the talus mid-talar axis and the first metatarsal first metatarsal axis typically Mearys angle is 0 with abnormal values considered angle 4 convex upward pes cavus angle -4 convex downward pes planus It can be used to classify the severity of deformity
3 lateral talocalceneal angle the angle between the calcaneal inclination axis and the mid-talar axis The lateral talocalcaneal angle should normally measure between 25 and 40 40 diagnoses flatfoot deformity12
4 Talonavicular coverage angle it is the medial angle between talar head articular surface and Proximal navicular articular surface Interpreting the talonavicular coverage angle 13Normal 7Adult Acquired flatfoot disease 7

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None