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Fractures, Bone clinical trials

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NCT ID: NCT03242733 Recruiting - Hip Fractures Clinical Trials

Ultrasound Assessment of Gastric Contents in Fasted Elderly Patients With Hip Fracture

Start date: December 26, 2017
Phase:
Study type: Observational

Evaluation of gastric contents in fasted elderly patients with hip fracture. The gastric contents will be examined by using ultrasonography in fasted elderly patients scheduled for hip fracture surgery. The primary outcome is the number of patients with stomach contents, and the secondary outcome is the component of residual gastric contents.

NCT ID: NCT03232216 Recruiting - Clinical trials for Vitamin D Deficiency

Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate?

ViDco
Start date: November 21, 2017
Phase: N/A
Study type: Interventional

This study evaluates the effect of Vitamin D3 supplementation in healing rate of tibia fractures in adult patients with low vitamin D. Half of participants will receive Vitamin D3 supplementation while the other will receive placebo.

NCT ID: NCT03224689 Recruiting - Clinical trials for Osteoarthritis, Knee

Evaluation of The Safety And Performance of The Freedom Total Knee® System With The PEEK-OPTIMA Femoral Component

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

Prospective, multi-centre, non-comparative, post-market surveillance clinical study

NCT ID: NCT03212768 Recruiting - Ankle Fractures Clinical Trials

Outcome of Low Energy Ankle Fractures

Start date: May 1, 2018
Phase:
Study type: Observational

Ankle fractures are among the most common osseous injuries to the lower extremity, and remain a significant source of morbidity for both the young and the elderly. Recent cross-national studies have shown a significant increase in the incidence and severity of ankle fractures among the elderly population.

NCT ID: NCT03197545 Recruiting - Stress Fracture Clinical Trials

Determining the Risk of Stress Fracture in IDF Soldiers Based on SNPs Identified for Osteoporosis

Start date: June 2017
Phase: N/A
Study type: Observational

The study is a genetic historical cohort study in a military combat recruits - this study does not examine a specific treatment but rather examines a statistical link between medical history of traumatic fractures, clinical diagnosis of stress fractures and the presence of unique SNPs in subjects DNA.

NCT ID: NCT03172715 Recruiting - Tibial Fractures Clinical Trials

Prosthesis Versus Osteosynthesis in Proximal Tibia Fractures

POSITIF
Start date: January 9, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to compare knee function and pain one year after treatment of intra-articular proximal tibia fracture using either osteosynthesis with a locking plate (ORIF) or primary total knee replacement (TKR) in patients over 65 years of age.

NCT ID: NCT03133195 Recruiting - Clinical trials for Unstable Intertrochanteric Fracture

The Effect of Teriparatide on Bone Union in Unstable Intertrochanteric Fracture Patients Treated With PFNA

Start date: May 17, 2017
Phase: Phase 3
Study type: Interventional

Phase III, prospective, randomized, parallel, double blind, placebo-controlled study to determine whether Teriparatide can accelerate bone healing in unstable intertrochanteric fracture patients treated with Proximal Femoral Nail Antirotation (PFNA) assessed by radiographic and clinical outcomes.

NCT ID: NCT03107767 Recruiting - Surgery Clinical Trials

Study of Re-operation Rate After Introduction of Evidence Based Algorithm for the Treatment of Ankle Fractures

PRO-Malleol
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

There is a high incidence of re-operations after surgery for ankle fractures. According to the Danish Fracture Database (DFDB) the re-operation rate, excluding hardware removal, is almost 10%. We are conducting a study on the efficacy of an evidence based algorithm for the treatment of ankle fractures.

NCT ID: NCT03097081 Recruiting - Spine Fracture Clinical Trials

ORthosis vs No Orthosis After Surgically Treated Traumatic Thoracolumbar Fractures

ORNOT
Start date: November 2016
Phase: N/A
Study type: Interventional

Rationale: There is no evidence in the current literature regarding the additional value of an orthosis after surgically treated thoracolumbar spine fractures. Objective: To assess whether an orthosis provides additional pain relief compared to no orthosis after posteriorly fixated thoracolumbar spine fractures. Primary outcome is difference in pain at six weeks post-operatively. Secondary objectives are pain at other moments, pain medication used, pain related disability, quality of life, long-term kyphosis, possible complications, hospital stay, return to work and subjective feeling on benefit or disadvantage from the orthosis. Study design: Randomized controlled intervention study, non-inferiority trial. Study population: Dutch speaking patients presented at the VU university medical centre, 18 - 65 years old with a traumatic thoracolumbar spine fracture from Th7 - L4 surgically treated by posterior fixation. Intervention: One group receives standard care and wears an orthosis after surgery for 12 weeks, to use when in vertical position. The intervention group does not wear an orthosis after surgery. Main study parameters/endpoints: Main study outcome is the difference in pain noted on the NRS-score at six weeks, ≥ 2 (SD 2,5) change corresponds with a clinically significant change in pain score. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The current guideline for postoperative care regarding dorsal stabilization of spine fractures recommends the use of a post-operative orthosis. While patients generally receive an orthosis for 12 weeks, individual surgeon's believes sometimes gives reason to deviate from this guideline. This is founded by literature that increasingly questions the use of orthoses in the conservative treatment of spine fractures. With the fracture operatively stabilized, the orthosis mainly provides support of gesture and thereby potentially results in pain relief and confidence for patients. On the other hand some patients have a hard time weaning from the orthosis or report discomfort due to the device and prefer not to use it. With subjects being randomized between the use of an orthosis or no orthosis there is no additional risk. This is in part because it is hypothesized that there is no difference in postoperative pain and there might be a lower risk of complications related to the orthosis.

NCT ID: NCT03094481 Recruiting - Clavicle Fracture Clinical Trials

Interscalene vs. Superficial Cervical Block vs. Combination for Analgesia After Clavicle Fracture

Start date: October 21, 2016
Phase: N/A
Study type: Interventional

The optimal analgesic peripheral nerve block (or combinations thereof) are undefined for clavicle fractures, the most frequent fracture in the human population. This goal of this study is to determine whether interscalene block (ISB), superficial cervical plexus block (SCPB), or both provide the best analgesia for lateral and midshaft clavicular fractures, respectively.