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Fractures, Closed clinical trials

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NCT ID: NCT03082872 Completed - Finger Fracture Clinical Trials

Cemented K-wire Fixation vs Open Transfixion Pinning

Start date: January 1, 2009
Phase: N/A
Study type: Interventional

To introduce a novel external-fixation technique using the combination of K-wires and cement, and the objective of this report is also to compare the technique with conventional open transfixion pinning.

NCT ID: NCT03031015 Completed - Clinical trials for Closed Fracture of Finger

Cemented K-wire Fixation vs Plating for Finger Fractures

CKFPFF
Start date: January 1, 2011
Phase: N/A
Study type: Interventional

To introduce a novel external-fixation technique using the combination of K-wires and cement. For comparison, we also included another group of patients who were treated using a mini plate and screw system. Bone healing, range of motion of the fingers, costs of treatments, and patient satisfaction were assessed.

NCT ID: NCT02951468 Completed - Clinical trials for Fracture, Healed, Fibrous Union

Mid-term Outcome Following Revision Surgery of Clavicular Non- and Malunion

Nonunion
Start date: January 2010
Phase: N/A
Study type: Observational

Background Treatment of clavicular non- and malunion is still challenging. Current surgical procedures often result in partially frustrating functional outcome along with high-grade subjective impairment and increased rates of revision surgery. However, the combination of vital bone graft and a biomechanically sufficient fixation system seems to be a promising concept of treatment. Methods In this retrospective study, 14 patients with a mean age of 44 years (26-67 years) suffering from non-union (n=11) and/or malunion (n=4) of the clavicle were enrolled. All patients were surgically treated using an anatomical precontoured locking compression plate (LCP) and autologous iliac crest bone graft. Functional outcome was assessed using the age- and sex-specific relative Constant Score.

NCT ID: NCT02762071 Completed - Osteoarthritis Clinical Trials

Liposomal Bupivacaine for Pain Control After Total Shoulder Arthroplasty

Start date: April 2016
Phase: N/A
Study type: Interventional

This study will compare interscalene nerve block versus liposomal bupivacaine (Exparel) for pain control after total shoulder replacements. Each method will be assessed in terms of post operative pain scores, pain medication consumption, length of stay, complications (nerve injuries, hematomas, cardiac/respiratory events) and rate of readmission due to pain. The aims of this study will be achieved through a randomized controlled trial and cost-effectiveness analysis.

NCT ID: NCT02670629 Completed - Radius Fractures Clinical Trials

Management of Distal Radius Fractures in Children Younger Than 11 Years Old.

Start date: January 2013
Phase: N/A
Study type: Interventional

This fractures have been managed with anatomical reduction performed under anesthesia or using sedatives. In our institution this means prolonged hospital stay, involvement of an anesthesiologist and the use of an special room in the Emergency Department. This research protocol was born after reports were published regarding leaving the fractures in an overriding position and cast with good functional and acceptable radiographical results; said study was observational, providing valuable but limited information about this treatment option. On the other hand, our study is a randomized controlled trial between to groups of patients younger than 11 years old who presented to the Emergency Department with completely displaced distal radius fractures, they were randomly assigned to one of two groups, either a closed anatomic reduction and short cast or a closed overriding alignment and short cast.

NCT ID: NCT02621255 Completed - Clinical trials for Closed Fracture of Hip

Effect of Anesthesia in Fracture Healing

Start date: November 2015
Phase: Phase 4
Study type: Interventional

Investigator' s study designed to investigate effect of general and regional anesthesia on fracture healing.The 40 age and older ASAI-III patients who will operate due to femur fracture (except femur neck fracture) will be enrolled in this study after informed consent approval. Subjects will be divided into two groups by a computerized randomization method. 40 patients will be enrolled in this study. General anesthesia will perform for 20 patients. Regional anesthesia will perform for 20 patients. Preoperative, 4. week and 12. weeks laboratory test which include blood and urine β-C terminal telopeptid (β-CTX), blood alkaline phosphatase and osteocalcin will test for all patients. All patients will not use nonsteroid anti-inflammatory drugs during study neither perioperative nor postoperative periods. fracture healing will be asses with clinical evaluation and laboratory tests.

NCT ID: NCT02390856 Completed - Fractures, Closed Clinical Trials

Volar Plate vs. Conventus DRS Fixation

Start date: February 2015
Phase: N/A
Study type: Interventional

Open reduction and internal fixation (ORIF) of unstable distal radius fractures is performed using a variety of fixation techniques. The most common method is fixed angle volar plate application. The investigators plan to compare the outcomes of fixed angle volar plating with a novel FDA approved intramedullary fixation device, Conventus DRS.

NCT ID: NCT02312128 Completed - Clinical trials for Closed Fracture of Lower End of Radius and Ulna

Early Mobilization of Operatively Stabilized Distal Radius Fractures - a Randomized Controlled Trail

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

The purpose of this study is to evaluate if an early mobilization after distal radius fractures treated by surgery leads to an better functional outcome then immobilization after surgery for 5 weeks in a cast

NCT ID: NCT02256059 Completed - Clinical trials for Fracture, Closed, Comminuted, Healing

Treatment of Displaced Lateral Clavicle Fractures Using a Locking Compression Plate With Lateral Extension

LatClav
Start date: June 2011
Phase: N/A
Study type: Observational

Treatment of lateral fractures of the clavicle is challenging and has been controversially discussed for a long time due to high non-union rates in non-operative treatment and high complication rates in surgical treatment. A recently developed implant was proven to ensure a biomechanically sufficient fixation of fractures leading to bony union and promising functional outcome in a small collective of patients.

NCT ID: NCT02188836 Completed - Clinical trials for Fracture, Closed, Comminuted, Healing

Electromagnetic Stimulation as Coadjuvant in the Healing of Diaphyseal Femoral Fractures

Start date: January 2008
Phase: Phase 3
Study type: Interventional

This study specifically evaluates the effects of electromagnetic stimulation for diaphyseal femur fractures using a device developed by the investigators. The hypothesis is that patients with femoral diaphysis treated with the electromagnetic stimulation have less non-union after six months than patients treated with a placebo device.