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Fractures clinical trials

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NCT ID: NCT00254631 Completed - Fractures Clinical Trials

Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures

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

We would like to check whether pre-operative administration of an oral controlled-release opioid formulation (Oxycodone hydrochloride (OxyContin)) could result in a clear effect of preemptive analgesia.

NCT ID: NCT00249743 Completed - Accidental Falls Clinical Trials

Clinical Evaluation of a Wireless Monitoring Device to Reduce Falls in the Elderly and Others at High Risk of Falling

Start date: December 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Falls are a public health problem of significant social and economic significance. No primary intervention devices have been shown to be effective in reducing falls and associated injuries. The objective of this study was to determine whether the new wireless FallSaver device reduces falls and fall-related injuries in elderly skilled nursing facility (SNF) residents. A randomized, prospective, open-label, cross-over study was conducted over a six-month period. The FallSaver device reduced the frequency of falls by 50% and fall-related injuries by 82% in 43 elderly at-risk SNF residents studied over 4,222 patient-days. The device and associated patch enclosure was well tolerated and devoid of serious problems. Significant cost savings and fewer reductions in quality of life are possible if fall-related injuries can be reduced.

NCT ID: NCT00235404 Completed - Asthma Clinical Trials

Randomized Controlled Trial of Health Care to Elderly Patients.

Start date: September 2003
Phase: N/A
Study type: Interventional

To study the efficacy of multicomponent treatment and care for patients with acute illness or deterioration of a chronic disease at a nursing home in primary health care compared to traditional treatment at hospital.

NCT ID: NCT00152321 Completed - Osteoporosis Clinical Trials

Strategies Targeting Osteoporosis to Prevent Recurrent Fractures

Start date: September 2003
Phase: N/A
Study type: Interventional

An evidence-based quality improvement intervention will overcome multiple barriers to best practice and improve rates of diagnosis and effective treatment for osteoporosis in high-risk patients. The intervention will be directed at patients (education and counseling) and their primary care physicians (reminders and opinion leader generated and endorsed single page guidelines)

NCT ID: NCT00137085 Completed - Anesthesia Clinical Trials

Ketamine Versus Fentanyl as an Adjunct to Propofol-Assisted Emergency Department Procedural Sedation

Start date: September 2004
Phase: N/A
Study type: Interventional

We, the investigators at Queen's University, propose to conduct a randomized, double-blind, feasibility trial comparing low-dose ketamine versus fentanyl as adjuncts to Emergency Department procedural sedation with propofol. The outcomes of interest will be safety, with respect to hemodynamic and respiratory adverse effects, as well as efficacy, with respect to adequacy of sedation and analgesia, recovery profiles and patient/physician satisfaction. Our hypothesis, based on a review of existing anesthesia literature, is that low-dose ketamine may be a safer and more efficacious alternative to fentanyl when used as an adjunct to propofol-assisted procedural sedation.

NCT ID: NCT00129142 Completed - Prostate Cancer Clinical Trials

Toremifene Citrate for Prevention of Bone Fractures in Men With Prostate Cancer on Androgen Deprivation Therapy

Start date: October 2003
Phase: Phase 3
Study type: Interventional

Androgen deprivation therapy (ADT) treatment for prostate cancer decreases the natural hormone called testosterone. This type of therapy is very effective for the treatment of prostate cancer. However, one of the side effects is bone loss or thinning of the bones that can lead to osteoporosis and an increased risk of bone fractures (breaking of the bones). The purpose of the study is to determine whether or not the addition of toremifene citrate (the study drug) to therapy can prevent or decrease the number of bone fractures and to evaluate its impact on side effects associated with testosterone reduction therapy.

NCT ID: NCT00114556 Completed - Osteoporosis Clinical Trials

The Effect of Zoledronic Acid on Bone Density in Liver Transplant Patients

Start date: February 2000
Phase: Phase 4
Study type: Interventional

Following liver transplantation, rapid bone loss occurs, particularly within the first 6 months post-transplant. This may be associated with fractures, most notable vertebral. The ability to assess osteoporosis therapies in this system may provide useful information for osteoporosis management in general. Hypotheses: 1. That treatment with the bisphosphonate, zoledronate, at the time of liver transplantation and at 1 month post-transplantation will prevent the early transplant-related bone loss (measured by bone densitometry and biochemical bone markers at 3 months) seen in patients who are not treated with a bisphosphonate 2. That continuing treatment with zoledronate at 3 monthly intervals for a total duration of 12 months will result in further improvements in bone density beyond that seen at 3 months 3. That calcium and vitamin D (vit D) supplementation of liver transplant patients does not prevent marked bone loss following transplantation.

NCT ID: NCT00079521 Completed - Osteoporosis Clinical Trials

Therapeutic Touch for Wrist Fractures in Postmenopausal Women

Start date: March 2003
Phase: Phase 2
Study type: Interventional

This study will evaluate the effectiveness of therapeutic touch in treating wrist fractures in women past menopause.

NCT ID: NCT00060970 Completed - Muscle Weakness Clinical Trials

Evaluating Muscle Function After Ankle Surgery

Start date: September 1995
Phase: N/A
Study type: Observational

Patients who are forced to rest or reduce activity as a result of illness, injury, or surgery often experience resulting muscle weakness. This study will evaluate muscle features and muscle strength in patients who are recovering from surgery for broken ankles. The goal of this study is to improve the recovery of muscle function and overall ability after prolonged periods of ankle inactivity due to surgery.