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Shoulder Fractures clinical trials

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NCT ID: NCT03573765 Completed - Osteoarthritis Clinical Trials

Epidemiology and Outcomes of Upper Limb Surgery: Analysis of Routine Data

Start date: April 6, 1998
Phase:
Study type: Observational

Surgery is a common treatment type for damaged joints, tendons and nerves in the upper limb where conservative measures are inappropriate or have failed. These conditions are common and result in significant levels of pain and functional disability. The investigators are conducting a broad ranging study of variation in the provision of surgical treatment and factors affecting outcomes after surgical treatment of upper limb conditions. This will be a population-based study of all patients undergoing surgical treatment funded by the National Health Service (NHS) of England over a nineteen-year period. This study will help to understand the factors associated with a poor outcome following surgery, which can be shared with patients considering treatment options. The investigators will also document current and future health service burden associated with commonly performed surgical procedures including complications and repeat operations.

NCT ID: NCT03567954 Terminated - Rotator Cuff Tear Clinical Trials

The Accuracy of Ultrasound in Detecting Rotator Cuff Tears in Proximal Humerus Fracture Patients

Start date: June 22, 2018
Phase:
Study type: Observational

The aim of this study is to determine the diagnostic accuracy of ultrasonography (US) in detecting full-thickness (a lesion that extends through both the bursal and articular part of the tendon) rotator cuff tear in patients who have sustained a proximal humerus fracture, using operative examination as the golden standard.

NCT ID: NCT03531463 Active, not recruiting - Clinical trials for Proximal Humeral Fracture

The Nordic DeltaCon Trial for Displaced Proximal Humeral Fractures in Elderly

DeltaCon
Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The Nordic DeltaCon Trial is a prospective, single-blinded, randomized, controlled, multi-center and multi-national trial comparing reverse prosthesis and non-operative treatment in displaced proximal humerus fractures, in the elderly patients aged 65 to 85 years with displaced OTA/AO group B2 or C2 fractures (According to the new 2018 revision: AO/OTA (Orthopaedic Trauma Association) group 11-B1.1, 11-B1.2 and 11-C1.1, 11-C3.1. )

NCT ID: NCT03498859 Completed - Clinical trials for Proximal Humeral Fracture

Efficacy of Physiotherapist-supervised Rehabilitation After Proximal Humerus Fracture

Start date: April 24, 2018
Phase: N/A
Study type: Interventional

This study investigates the efficacy of physiotherapist-supervised training once per week during 10 weeks compared to home-based training during 10 weeks, after proksimal humerus fracture.

NCT ID: NCT03489408 Terminated - Clinical trials for Humeral Fractures, Proximal

Post-Approval Prospective Study - Conventus CAGEā„¢ PH for Use in Proximal Humerus Fracture Fixation

Start date: February 1, 2018
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to collect device and procedure experience in everyday clinical practice. The patients are being asked to participate in this study because they are a surgical candidate for the treatment of a broken shoulder and are considering treatment with the PH Cage device.

NCT ID: NCT03464578 Completed - Clinical trials for Proximal Humeral Fracture

Evidence Based Algorithm for Proximal Humerus Fractures

Start date: January 1, 2014
Phase:
Study type: Observational [Patient Registry]

Proximal humerus fractures are particularly frequent injuries and represent 6% of all fractures with an overall incidence of 63/100.000 in human. The goal is to assess our institutional evidence based algorithm for treatment of proximal humeral fractures. Objective(s): 1. Test the algorithm in terms of clinical applicability and clinical outcome 2. Compare general outcome and general complication/revision rate to the literature. Inclusion / Exclusion criteria: Inclusion: All patients with an acute proximal humeral fracture (not older than 48 hours) admitted to our institution later than 1.1.2014. Exclusion: Multilevel and pathological fractures are excluded. Terminally ill patients and those not being able, or willing to sing the informed consent. Project Centre(s): Single-centre. Statistical Considerations: Standard descriptive statistics will be performed using R-statistics program. Considering the population of 160 patients, we will be able to detect differences in proportions as low as 0.15 with power 82% and alpha = 0.05. Other methodological Considerations: Terms applicability of a treatment protocol and adhesion to protocol are not well defined for decision making in orthopaedic surgery.

NCT ID: NCT03427112 Completed - Clinical trials for Proximal Humeral Fracture

Assessment of the Surgical Handling and Performance of the X-ray-based Tracking and Navigation System "Xin1 Humerus System" Evaluated From 10 Proximal Humerus Plate Fixations

Start date: April 4, 2017
Phase:
Study type: Observational [Patient Registry]

Xin1 Humerus system is an X-ray-based tracking and navigation system designed to calculate the plate position and all required proximal screw lengths for proximal humerus plate fixation. The aim is to validate the system performance in a clinical context and test the surgical handling of the Xin1 marker in a hospital environment. 10 adults having sustained a proximal humerus fracture and are indicated for plate fixation osteosynthesis will be provided intraoperatively with the Xin1 marker. The system performance is evaluated retrospectively by post-processing the intraoperative X-ray images after surgery

NCT ID: NCT03383991 Completed - Clinical trials for Humeral Fracture, Proximal

Reverse Total Shoulder Arthroplasty Versus Hemiarthroplasty for Displaced 3- and 4-part Proximal Humeral Fractures

Start date: September 10, 2013
Phase: N/A
Study type: Interventional

Proximal humeral fractures are common injuries with the highest incidence being amongst the elderly. Most proximal humeral fractures are nondisplaced or minimally displaced. The majority of these are reliably treated nonoperatively with an acceptable functional outcome. The treatment of displaced fractures is more controversial. Consensus is lacking as to when surgery is indicated or what type of procedure to choose if surgery is elected. Displaced 3- and 4-part fractures where internal fixation is deemed unreliable have been considered an indication for hemiarthroplasty. Hemiarthroplasty gives reasonable control of pain but the resulting shoulder function and range of motion is unpredictable. The use of reverse total shoulder arthroplasty is increasing and might result in a better range of motion then hemiarthroplasty. The aim of this multicenter study is to test the hypothesis that reverse total shoulder arthroplasty gives better shoulder function than hemiarthroplasty for displaced 3- and 4-part proximal humeral fractures.

NCT ID: NCT03382665 Terminated - Clinical trials for Rheumatoid Arthritis

Post-market Surveillance Study With the HYPERION Hip Endoprosthesis System in Defect Reconstruction

Start date: January 2010
Phase:
Study type: Observational

The study is a multi-center, prospective, non-controlled, consecutive cohort post market surveillance study. The objective of this study is to obtain survival and clinical outcome data on the Hyperion® system in primary and revision total hip arthroplasty.

NCT ID: NCT03358784 Not yet recruiting - Clinical trials for Humeral Fracture, Proximal

Comparison of Hemi-shoulder Arthroplasty and PHILOS in Treating Three or Four-part Fractures of Proximal Humerus

Start date: March 5, 2018
Phase: N/A
Study type: Observational

To explore clinical effectiveness of PHILOS plate fixation and hemi-shoulder arthroplasty in treating three or four-part fractures of proximal humerus