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Fractures, Bone clinical trials

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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: NCT04546503 Completed - Limb Fracture Clinical Trials

Impact of Continuous Regional Analgesia in Severe Trauma Patients

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

Regional analgesia, based on its physiological effects and efficacy, is used for optimal perioperative pain relief. However, for acute pain in multiple trauma patients in a critical condition, it has not been prospectively studied. The use of regional anaesthesia in this group of patients extend to the management of trauma patients and of other painful procedures performed at the patient's bed. The use of RA in such patients must be analyzed in the light of associated conditions that can increase the risk of systemic toxicity and complications: coagulopathies, infection, immunosuppressive states, sedation and problems associated with mechanical ventilation. The investigators aim to assess the role of continuous peripheral nerve blocks (CPNB) in multiple trauma patients, in order to show the benefits in terms of opiates consumption decrease, sedation limitation, improvement in ventilator free days and patients outcome

NCT ID: NCT04536311 Completed - Anesthesia, Local Clinical Trials

Surgical Stabilization of Rib Fractures While Awake or Under Appropriate Sedation by Paravertebral Block

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Tracheal intubation and general anesthesia has been considered a safe and conventional routine methodology for thoracic surgery, include multiple rib fratcure. However,adverse effects such as sore throat, pain, hoarseness, and respiratory complications are common after that. In this study, we decide to perform surgical stabiliazation of rib fractures by paravertebral block surgical stabiliazation of rib fractures under awake or appropriate sedation without endotracheal intubation keeping spontaneous respiration to investigate its safety and feasibility.

NCT ID: NCT04532580 Completed - Fracture Clinical Trials

Clinical Validation of Boneview for FDA Submission

Start date: September 1, 2020
Phase:
Study type: Observational

The goal of this clinical validation is to assess comparative performances of physicians with and without the assistance of BoneView for the diagnosis of fractures on radiographs. The performances are evaluated in terms of accuracy (primary endpoint with the pair specificity/sensitivity and the secondary endpoint PPV/NPV) and in terms of time needed for diagnosis (secondary endpoint with the measurement of time on each case).

NCT ID: NCT04520555 Completed - Clinical trials for Laryngeal Mask Airway

Flexible Laryngeal Mask Airway Versus Tracheal Intubation in Nasal Bone Fracture

Start date: July 13, 2020
Phase: N/A
Study type: Interventional

In surgery under general anesthesia due to nasal bone fracture, laryngeal mask airway or tracheal intubation has been used. However, it has not been investigated that the difference of recovery profiles according to use of laryngeal mask airway or tracheal intubation in nasal bone fracture surgery. The aim of study is to evaluate the efficacy of the laryngeal mask airway regarding recovery profiles and airway complications, compared to tracheal intubation.

NCT ID: NCT04518956 Completed - Clinical trials for Mandibular Fractures

Shockwave Therapy Versus LIPUS on Mandibular Fracture Bone Healing

Start date: December 18, 2016
Phase: N/A
Study type: Interventional

compare between the effect of shockwave therapy and low-intensity pulsed ultrasound on healing process of fresh mandibular fractures

NCT ID: NCT04514601 Completed - Orthopedic Disorder Clinical Trials

A Quality Improvement Project to Assess and Refine the Handover Process at Morning Trauma Meetings

Start date: October 23, 2019
Phase:
Study type: Observational

This project was intended to observe the handover of trauma and orthopaedic patients at a district general hospital in the UK. Following the implementation of a standard operating protocol, the handover of patient information improved including neck of femur fracture patients significantly. The study can therefore be utilised by other similarly structured departments to improve the handover process, thereby improving patient safety.

NCT ID: NCT04509895 Completed - Calcaneus Fracture Clinical Trials

Minimally Invasive Calcaneal Fracture Fixation vs Standard Lateral Approach

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

a comparison between the standard lateral extensile approach and minimally invasive sinus tarsi approach in this research.

NCT ID: NCT04498923 Completed - Postoperative Pain Clinical Trials

Duration of Blockade of Peripheral Nerves With Bupivacaine Depending of the Adjuvants

DBBA
Start date: January 1, 2018
Phase:
Study type: Observational

The main aim of the investigator's study is to propose combination of local anesthetics and adjuvants that provides both adequate anesthesia during surgery and prolonged post-operative analgesia.

NCT ID: NCT04495400 Completed - Clinical trials for Lumbar Vertebral Fracture

Percutaneous Screw Fixation vs. Open Fixation in the Treatment of Thoracolumbar Fractures

PrecScrew
Start date: April 23, 2018
Phase:
Study type: Observational

In this single-center retrospective study, the investigators will include all patients admitted to Parkland Hospital who underwent surgical fixation of thoracolumbar fractures between the years 2000 and 2017. The study investigators will gather demographic, radiographic, and operative information. Patients will be matched according to demographic information in a case-control style. The primary outcome of the study will be comparing the clinical and radiographic outcomes of two surgical techniques in order to establish the best treatment approach for this disease.