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Humeral Fractures clinical trials

View clinical trials related to Humeral Fractures.

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NCT ID: NCT04780308 Completed - Clinical trials for Supracondylar Humerus Fracture

Pediatric Type III Supracondylar Humeral Fracture

Fracture
Start date: January 1, 2010
Phase:
Study type: Observational [Patient Registry]

The purpose of this study was to compare pin configuration effects on early secondary displacement in the surgical treatment of pediatric supracondylar humeral fractures (SCHF).

NCT ID: NCT04694469 Completed - Morbidity Clinical Trials

Comparison of Day-time and Night-time Operations of Supracondylar Humeral Fractures

Start date: June 26, 2019
Phase:
Study type: Observational

This study aims to investigate that performing supracondylar humerus fracture operations during daylight hours may have better results than performing them at night.

NCT ID: NCT04675879 Completed - Clinical trials for Proximal Humeral Fracture

Clinical and Radiological Results of Conservative Treatments in Proximal Humerus Fractures.

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

In the investigators' prospective randomized study, the investigator will investigate the effect of different bandage types on functional and radiological results of proximal humerus fractures over 18 years of age, for whom conservative treatment is decided. In recent studies, it has been shown that surgical treatment in proximal humerus fractures has a high complication rate and is also not superior to conservative treatments in terms of functional results. Therefore, the importance of conservative treatment is increasing day by day in this group of fractures, especially in elderly patients with high risk for surgery. In these studies in the literature, the method in conservative treatment is not clearly specified, and the investigator will apply 3 different bandages to adjust the rotation of the shoulder in 3 different ways during the investigators' conservative treatment. The investigator will compare functional and radiological results between these groups.

NCT ID: NCT04622852 Completed - Clinical trials for Proximal Humeral Fracture

Pegs for Osteofixation of Proximal Humeral Fractures

Start date: July 1, 2017
Phase:
Study type: Observational

Patients treated operative for Proximal humeral fractures with angular stable device (Philos plate or ALPS-PHP)

NCT ID: NCT04582123 Completed - Clinical trials for Supracondylar Humerus Fracture

Comparison of Cross Pin Configurations in Supracondylar Humerus Fracture Treatment: 2 Pins Versus 3 Pins

Start date: January 15, 2015
Phase: N/A
Study type: Interventional

The objective of this prospective randomized controlled trial is to evaluate and compare the outcome of the 2wire vs 3 wire crossed pin configurations in the management of supracondylar humeral fractures in children.

NCT ID: NCT04553497 Completed - Clinical trials for Interferential Current in Proximal Humerus Fractures

IFC Therapy in Proximal Humerus Fractures

Start date: April 1, 2014
Phase: N/A
Study type: Interventional

Proximal humerus fractures (PHFs) frequently occur in the elderly and osteoporotic population, but these fractures are also common in individuals under age 60 years. Conservative treatment of PHF usually involves a short period of immobilization followed by orthopedic rehabilitation. However, the severe pain of some patients with fractures limits their participation in the exercise programme, and shoulder muscle atrophy and frozen shoulder may occur in these patients due to immobilization. There are conflicting results regarding the use of physical therapy modalities in the shoulder pain management. Interferential current (IFC) therapy is believed to be effective for the pain-relieving through several mechanisms. Although IFC has been investigated in many painful shoulder disorders, there is no reported study on the effectiveness of IFC therapy in patients with PHF. This study aimed to investigate the effectiveness of IFC added to exercise on shoulder function, pain, and disability compared with placebo in patients with conservative treated PHF. Patients were evaluated within the first week of PHF and divided into two groups to receive either IFC or sham using a simple randomization method. The orthopedic rehabilitation programme was applied to all patients three times a week for four weeks under the guidance of the same physiotherapist. IFC or sham therapy was applied three times a week for 20 minutes before each exercise session by another physiotherapist. Shoulder functions, pain (visual analogue scale), disability and range of motion was evaluated at the end of the rehabilitation program, at 6-weeks and 18-weeks post-treatment by the physiatrist (ED) who did not know which group the patients belonged to. In addition, the amount of acetaminophen usage was noted at each visit.

NCT ID: NCT04538118 Completed - Rotator Cuff Tears Clinical Trials

Relationship of Patient-Specific Functional Scale With Shoulder Functions: A Prospective Study

Start date: January 5, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to examine the relationship between the Patient- Specific Functional Scale (PSFS) and shoulder functions in the physiotherapy and rehabilitation program applied to patients with shoulder problems.

NCT ID: NCT04216017 Completed - Humeral Fractures Clinical Trials

Glenohumeral Cortisone Injection

Start date: January 1, 2020
Phase: Phase 2
Study type: Interventional

The objective of this project is to determine if giving a cortisone injection to patients with proximal humerus fractures who have stiff shoulders recover their range of motion.

NCT ID: NCT04056351 Completed - Clinical trials for Proximal Humeral Fracture

A Research Study to Understand and Predict the Failure of Shoulder Fracture Fixations Using Computer Simulations

PHILOS-SIM
Start date: August 2, 2019
Phase: N/A
Study type: Interventional

Fractures of the shoulder, the so-called proximal humeral fractures, can be treated with locking plates that have shown good results in clinical practice, but complications can occur. In order to further improve the treatment of proximal humerus fractures and decrease the rate of fixation failures, further research is necessary. As a first step, the reasons for potential implant failures need to be understood. This study has been initiated by scientists at the AO Research Institute Davos (ARI), Switzerland, which is the research center of the AO Foundation (www.aofoundation.org), an international non-profit organization led by surgeons specialized in fractures such as these. Researchers at the ARI have been developing a computational simulation tool to predict fixation failure and demonstrated its efficiency in laboratory conditions. This clinical study has been organised to validate this tool using patient data, by comparing the risk of mechanical failure predicted by the computer simulated model with the clinically observed fixation failure. In future, this computer simulation tool is expected to help surgeons to select the best fixation for a given patient and to develop improved implants.

NCT ID: NCT03919422 Completed - Clinical trials for Proximal Humeral Fracture

Paravertebral Block for Proximal Humeral Fracture Surgery

Start date: May 5, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effects of T2 paravertebral block block improving interscalene brachial plexus block and superficial cervical plexus block on the relief of pain intensity during elderly proximal humerus fracture fixation surgery. The brachial plexus and cervical plexus block(IC block) will be performed in half of participants, while the T2 paravertebral block combined with IC block will be performed in the other half.