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Fractures, Bone clinical trials

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NCT ID: NCT03642808 Active, not recruiting - Clinical trials for Osteoporotic Fractures

Optimisation of Falls Prevention After Low-energy Osteoporotic Fractures: Feasibility Study

OPTICHUTE
Start date: July 27, 2018
Phase: N/A
Study type: Interventional

Within the Groupe Hospitalier Paris Saint-Joseph (GHPSJ), a reinforced medical care of osteoporosis ('Fracture Liaison service') was organized for osteoporotic fractured patients. The evaluation of benefits of this program through a randomized study showed an improvement in diagnostic tests performed (bone densitometry) and antiosteoporotic treatment initiated (OPTIPOST study, being published in BMJ). However, of 323 patients included, 91 presented a new fracture within 12 months. Among them, 40/126 patients (31.7%) were in the reinforced medical care arm. This result clearly demonstrates the need for a specific medical care program for patients with osteoporotic fracture falling regularly.

NCT ID: NCT03640039 Not yet recruiting - Mandible Fracture Clinical Trials

Comparative Study Evaluating Stability of Fracture Segments After Treatment of Mandibular Angle Fracture With 3d Strut Plate With or Without IMMF.

Start date: January 11, 2019
Phase: N/A
Study type: Interventional

comparative study evaluating stability of fracture segments in mandibular angle fracture with 3d strut plate with or with out post operative IMMF.

NCT ID: NCT03639272 Completed - Talus Fracture Clinical Trials

Treatment of Talus Fractures: a Retrospective Study

TTF2017
Start date: January 1, 2007
Phase:
Study type: Observational

The main purpose of this retrospective case series study was to evaluate long-term radiographic and clinical outcomes of a consecutive series of patients with diagnosis of isolated, displaced, closed talar neck or body fractures treated by open reduction and internal fixation. Secondly, it was aimed to verify the influence of the location of talar fractures on the outcomes, the prognostic value of the Hawkins sign, whether operative delays promote avascular necrosis (AVN) and if the fractures require emergent surgical management.

NCT ID: NCT03638674 Active, not recruiting - Bone Fracture Clinical Trials

Evaluation of Agreement Between CT Scan and 3D-DXA Measurements on the Lombar Spine

3D DXA SPINE
Start date: February 26, 2019
Phase: N/A
Study type: Interventional

Dual-energy X-ray Absorptiometry is frequently used to measure bone mineral density. A new medical device, Box 3D DXA, creates a 3D image using a statistics reconstruction model developed on the femur. This new imaging technique does not require additional irradiation and ought to improve bone measures as well as incorporating densitometric parameters into the diagnosis. This study will test the reconstruction of the 3D image from lombar spine measurements and compare accuracy against measurements made using CT scan.

NCT ID: NCT03637621 Active, not recruiting - Clinical trials for Distal Humerus Fracture

Retrospective Analysis on Distal Humerus Fractures

(DHFx)
Start date: January 7, 2018
Phase:
Study type: Observational

The purpose of this study is to evaluate preoperative objective measurements for distal humerus ORIF patients and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 18 years old or greater at the time of surgery were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

NCT ID: NCT03637608 Active, not recruiting - Clinical trials for Proximal Humeral Fracture

Proximal Humerus Fractures: A Retrospective Analysis

PHFx
Start date: December 7, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate preoperative objective measurements of patients with a proximal humerus fracture and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 18 years old or greater at the time of open reduction, internal fixation surgery were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

NCT ID: NCT03636646 Not yet recruiting - Acetabular Fracture Clinical Trials

Analysis of the Posterior Wall Fracture of the Acetabulum

Start date: August 2018
Phase:
Study type: Observational

Assessement,evaluation of postoperativ reduction of posterior wall acetabular fractures in Assiut University Hospital

NCT ID: NCT03635060 Completed - Clinical trials for Distal Radius Fracture

Distraction Osteogenesis for Distal Radius Fractures vs. Volar Plating

DORSAL
Start date: September 12, 2018
Phase: N/A
Study type: Interventional

Optimal fixation for highly comminuted distal radius fractures with metadiaphyseal extension remains to be a major treatment challenge for orthopaedic surgeons. The purpose of this study is to determine the safety, feasibility and sample size estimations for a larger, definitive study comparing functional outcomes of patients treated with dorsal distraction plate fixation with or without fragment specific fixation to standard open reduction internal fixation in highly comminuted distal radius fractures (subtypes AO.23-C2 and AO.23-C3). The study design will be a pilot randomized control trial. Fracture pattern eligibility will be determined by consensus agreement between two fellowship trained upper extremity specialists. The primary outcome measure will be the QuickDASH score. Secondary outcome measures include wrist range of motion, grip strength, Visual Analog Scale pain scale, Short Form SF-12, and EQ-5D. Ultimately, this study will lead to a larger randomized control trial and result in improvement in the care and treatment of patients with these challenging injuries.

NCT ID: NCT03634865 Completed - Clinical trials for Radius; Fracture, Lower or Distal End

Screw Lengths in Radius Volar Plates

PESLDRF
Start date: January 25, 2018
Phase:
Study type: Observational

Background Fractures of the distal radius are among the most common. Major complications, including irritation and rupture of the extensor tendons, may occur if epiphyseal screws of inappropriate length are used. Questions/Purposes The main objective of the present study was to determine whether the optimal epiphyseal screw length can be determined by reference to the diaphyseal screw length. Methods Forty CT scans were semi-automatically segmented. A 3D model of the volar plate was affixed to each distal radius with simulation. The maximum lengths of the diaphyseal screws, as well as the four distal epiphyseal screws, were measured. Linear regression analysis was performed.

NCT ID: NCT03625154 Not yet recruiting - Ankle Fractures Clinical Trials

Operative Versus Non Operative Management Outcomes of Isolated Lateral Malleolar Weber B Ankle Fractures

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

The primary objective of this study is to determine the failure rate and difference in clinical outcomes between operative and non operative treatment of patients with Weber B lateral malleolus ankle fractures with medial clear space widening on gravity stress views. All patients presenting will be treated non operatively, and compared to an observational group comprised of patients with Weber B lateral malleolus ankle fractures without medial clear space widening, for which the standard of care is non operative management. Patients who decline non operative management and elect to undergo operative open reduction internal fixation with plates and screws will comprise an operative observational cohort. All patients will be followed for a total of 12 months from the time of injury. Clinical outcomes will be based on radiographic monitoring for ankle mortise congruency, as well as standardized SF-36 and AOFAS questionnaire scores.