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Fractures, Bone clinical trials

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NCT ID: NCT01615744 Completed - Os Calcis Fracture Clinical Trials

Surgical vs Conservative Treatment of Displaced Intra-articular Calcaneal Fractures: A Prospective RCT

Start date: December 1993
Phase: N/A
Study type: Observational

Between 1994-98 5 hospitals in Stockholm investigated calcaneal fractures in a randomised study. 82 patients were included and randomized either to non-surgical treatment or surgical management with extensile lateral approach and reduction with Internal fixation (ORIF) The patients were followed and investigated at fixed intervals 2 weeks, 8 weeks, 3 months and 6 months for clinical review. At 1 year and 8-12 years (mean 10 years) post-injury. Both clinical radiological data were collected and several scores were used. The primary outcomes scores used were SF-36 and VAS score. The results after 1 year and mean 10 years are presented.

NCT ID: NCT01612208 Completed - Clinical trials for Fracture of the Distal Femur

MotionLoc Study, Femur Fractures

Start date: April 2011
Phase: N/A
Study type: Observational

The objective of this study is to document callus formation and healing of fractures stabilized with locking plates utilizing modern MotionLoc screws that provide controlled axial micro-motion to actively promote fracture healing.

NCT ID: NCT01606540 Completed - Colles Fracture Clinical Trials

Non-steroid Antiinflammatory Drugs to Heal Colles Fracture

Start date: June 2012
Phase: N/A
Study type: Interventional

It is believed that some painkillers (NSAID drugs) slow bone healing but the knowledge is based only on experimental studies with animals whose results are automatically translated for humans. The purpose is to examine whether these drugs slow bone healing and what relationship there is between different bone examinations, scan for osteoporosis, bone marker laboratory tests, radiological controls and histology of newly formed bone under a microscope.

NCT ID: NCT01599403 Completed - Clinical trials for Traumatic Rib Fracture

Thoracic Blocks Versus Thoracic Epidural and Patient Controlled Anesthesia in Traumatic Rib Fracture Patients

Start date: April 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to investigate whether continuous PVB is equal in efficacy to epidural anesthesia in terms of analgesia in patients with INR lower than 1.2, or is continuous ICNB equal in efficacy to PCA in terms of analgesia, if patients have INRs equal to or greater than 1.2.

NCT ID: NCT01592604 Completed - Clinical trials for Closed Fracture of Base of Fifth Metatarsal Bone

An Optimal Treatment for Avulsion Fractures of the Base of Fith Metatarsal Bone

Start date: November 2011
Phase: N/A
Study type: Interventional

Avulsion fractures of the base (tuberosity) of fifth metatarsal bone are the most common fractures in the foot, frequently treated in fracture clinics and involving significant resources. At present methods of treatment and follow up vary widely from no active treatment to surgery, depending entirely on a treating doctor preference. There is no agreement on simple, safe and reliable method of treatment. The investigators believe that vast majority of these injuries heal well on its own without any specific treatment. By comparing two most commonly used treatments the investigators aim to establish one simple, safe and reliable mode of treatments. The investigators are going to evaluate functional results of these two treatments in a short and longer time prospective, by using the best available scientific tools. The investigators believe that results of the investigators study will eventually lead to change of practise and more efficient NHS care for these patients. It will reduce unnecessary treatments and clinic appointments, and bring substantial savings to the NHS in a long prospective.

NCT ID: NCT01589692 Completed - Clinical trials for Distal Radius Fracture

A Clinical Trial for the Surgical Treatment of Elderly Distal Radius Fractures

WRIST
Start date: April 10, 2012
Phase: N/A
Study type: Interventional

In the United States, over 300,000 individuals over age 65 suffer from distal radius fractures (DRFs) each year. Despite the frequency of this injury and over 200 years of experience treating DRFs, management of elderly DRFs is still controversial. Close reduction and casting is a nonsurgical technique that is frequently used, but osteoporotic fractures, common in the elderly, often collapse and displace. The three currently applied surgical techniques are close reduction and percutaneous pinning, external fixation with or without percutaneous pinning, and internal fixation with volar locking plating. Preliminary evidence indicates that locking plate fixation can permit elderly patients to move their hands and wrists much sooner in order to return to self-care activities more quickly. Although these outcomes are promising, there is no randomized controlled clinical trial to demonstrate that the more invasive, and perhaps more costly, plating technique is superior to the other simpler approaches. The specific aim of this 24-center randomized controlled trial is to compare outcomes of these three surgical techniques in treating unstable DRFs in the elderly. The secondary aim is to follow a cohort of elderly patients who choose not to have surgery to evaluate outcomes following treatment by close reduction and casting alone. This clinical trial is the most ambitious study in hand surgery by assembling most of the leading centers in North America to collect evidence-based data to guide future treatment of this prevalent injury in the growing elderly population.

NCT ID: NCT01583556 Completed - Clinical trials for Distal Radius Fracture

Optional Follow-up Visits for Common, Low-risk Arm Fractures

Start date: July 2012
Phase: N/A
Study type: Observational

Many common arm fractures have an excellent prognosis with little more than symptomatic treatment. When studying these fractures, investigators find that a substantial number of patients do not attend follow-up appointments. The difficulty of maneuvering in big cities, the cost of parking, the co-pay for the visit and the wait times for x-ray and doctor are all inconveniences that some patients might prefer to avoid. Building on prior research, it is appropriate to offer patients with common minor upper extremity fractures that have an excellent prognosis optional follow-up after the first visit. The plan would be to be available by phone, email and subsequent appointment at the patient's discretion if they felt that the recovery was off course. Benefit to individual participants is unlikely. The study will benefit the society as a whole, by providing a better understanding of these common fractures. It can also affect the economics of our health system by avoiding further follow-up appointments. Primary null hypothesis: There is no difference in patient outcome 2-6 months after injury between patients that return for a second visit, and patients that do not. Secondary null hypothesis: There is no difference in patient satisfaction 2-6 months after injury between patients that return for a second visit, and patients that do not.

NCT ID: NCT01578408 Completed - Clinical trials for Femoral Neck Fractures

Cemented Versus Uncemented Stems in Total Hip Arthroplasty in Patients With Femoral Neck Fractures

Start date: May 11, 2010
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized study is to compare the quality of treatment between cemented versus uncemented hydroxyapatite coated femoral stems in Total Hip Arthroplasty (THA) in patients who suffers from dislocated femoral neck fractures. Our hypothesis is that an uncemented option spares the patient the operative load of the cementing procedure, i e risk of fatty embolism and inflammatory response, which in turn also perhaps reduces the postoperative cognition strain and improves mobilization parameters. If the uncemented option has the same excellent fixation in poor bone stock, as in the case of these osteopenic fractures, and also has the same good clinical outcome, it would be a viable standard option for the treatment of dislocated femoral neck fractures.

NCT ID: NCT01576224 Completed - Clinical trials for Distal Radius Fracture

Early Mobilization After Volar Plate Osteosynthesis of Distal Radius Fractures

E-MOB
Start date: January 2012
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the post operational mobilization after volar locking plate osteosynthesis of distal radius fractures. One group is admitted training exercises just after the fracture treatment, one group after 14 days immobilization in a cast. The primary hypothesis is, that immediate training leads to earlier and faster recovery. Our second hypothesis is, that immediate training does not lead to increased risk of fracture displacement.

NCT ID: NCT01574833 Completed - Fracture Clinical Trials

Early Application of Pulsed Electromagnetic Field in the Treatment of Postoperative Delayed Union

Start date: March 2007
Phase: Phase 4
Study type: Interventional

The investigators hypothesized that early applied pulsed electromagnetic field treatment on delayed union might lead to increased rate of fracture union and shortened period of treatment.