Viewing Study NCT06590701



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06590701
Status: RECRUITING
Last Update Posted: None
First Post: 2024-05-29

Brief Title: Scapholunate Ligament Reconstruction Early Dart Throwing Motion Versus Motion in Anatomical Planes
Sponsor: None
Organization: None

Study Overview

Official Title: Scapholunate Ligament Reconstruction Early Dart Throwing Motion Versus Motion in Anatomical Planes
Status: RECRUITING
Status Verified Date: 2024-05
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: SL-Reko
Brief Summary: Patients undergoing scapholunate ligament reconstruction at Balgrist University Hospital are divided into two groups and receive two different types of mobilisation postoperatively The investigators will compare the outcome pain strength mobility between the two groups 1 year after the operation
Detailed Description: The so-called dart-throwing motion DTM plane of movement from radial extension to ulnar flexion has gained attention as it has been shown to be an important axis of wrist movement during activities of daily living Further studies have shown that during movement of the intact wrist in the dart throwing plane most of the movement occurs in the mediocarpal joint while the proximal row remains relatively immobile

In scapholunate SL ligament reconstruction using the flexor carpi radialis tendon the SL interval is immobilised using 2 Kirschner wires for 8-10 weeks to relieve the strain on the ligament and allow it to heal From the 2nd postoperative week mobilisation is started using DTM mobilisation or mobilisation in the anatomical plane The aim of the study is to investigate in a randomised trial whether mobilisation in the anatomical plane produces the same postoperative results

In this project the investigators will compare two types of mobilisation in the rehabilitation of SL ligament reconstruction The participants will be randomised to two treatment groups This procedure therefore corresponds to a risk category A in other clinical trials according to Chapter 4 ClinO

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