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NCT ID: NCT00616850 Withdrawn - Clinical trials for Total Knee Arthroplasty

Treatment of Postoperative Pain After Total Knee Arthroplasy Using Intravenous Lidocaine Infusion

Start date: October 2007
Phase: N/A
Study type: Interventional

Total knee replacement is often associated with severe postoperative pain, especially in the first 24 hours. Patient controlled analgesia (PCA) and continuous femoral block with PCA are commonly used to treat postoperative pain after total knee arthroplasty. However, PCAs use opioids. Opioids are excellent painkillers but their use is hampered by side effects such as nausea, vomiting, bowel dysfunction, urinary retention, pruritus, sedation and respiratory depression. We propose to test the hypothesis that adding a low dose lidocaine infusion to PCAs will lower the amount of opioids that these patients receive, thereby improving patient safety while still providing adequate analgesia. In addition, continuous femoral block has been shown to provide superior postoperative pain control when compared to morphine PCA. Therefore, postoperative pain levels of study subjects will be compared to those subjects who receive a combination of a continuous femoral block catheter with a PCA.

NCT ID: NCT00616590 Withdrawn - Clinical trials for Head and Neck Cancer

Insomnia in Patients Undergoing Chemotherapy and Radiation Therapy for Head and Neck Cancer

Start date: July 2007
Phase: N/A
Study type: Observational

RATIONALE: Learning about insomnia and quality of life in patients undergoing chemotherapy and radiation therapy for cancer may help doctors learn about the effects of treatment and plan the best treatment. PURPOSE: This clinical trial is studying insomnia in patients undergoing chemotherapy and radiation therapy for head and neck cancer.

NCT ID: NCT00615524 Withdrawn - Clinical trials for Hormone-receptor Positive Breast Cancer

Phase II Study Evaluating Exemestane Alone Or In Combination With Pazopanib In Postmenopausal Women With Hormone Receptor Positive Breast Cancer

Start date: April 2008
Phase: Phase 2
Study type: Interventional

This study is being conducted to compare the efficacy and safety of exemestane alone or in combination with pazopanib in postmenopausal women who have hormone receptor positive breast cancer and have failed therapy with tamoxifen, anastrazole or letrozole.

NCT ID: NCT00615381 Withdrawn - Clinical trials for Intracranial Aneurysm

Supraphysiologic Insulin to Improve Outcomes After Surgical Treatment of Unruptured Cerebral Aneurysms

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

We hypothesize that in patients undergoing surgical treatment of unruptured intracranial aneurysms, the increase in blood sugar as a result of surgical stress is detrimental to outcome, as measured by blood levels of proteins associated with systemic inflammation and 7 day, 90 day, and 1 year postoperative neurologic and neuropsychiatric outcomes. Because insulin itself is an anti-inflammatory agent, we anticipate that normalizing blood sugar levels with insulin doses higher than normally produced by the body (i.e., "supraphysiologic" insulin doses) will have a greater benefit on these outcomes than equally normalizing blood sugar levels using normal insulin doses. Based on the results of this study, we will be able to determine if a more laborious strategy to normalize blood sugar levels (i.e., "supraphysiologic" insulin therapy) offers any additional benefits to normal insulin dosing strategies. In addition, we will obtain a robust assessment of postoperative neuropsychiatric and neurologic outcomes of surgically repaired unruptured intracranial aneurysms that will serve as the basis for future studies to decrease morbidity of these patients

NCT ID: NCT00613977 Withdrawn - Clinical trials for Respiratory Distress Syndrome

Comparison of Two Fetal Lung Maturity Tests

Start date: January 2008
Phase:
Study type: Observational

The investigators wish to compare the difference in both cost and time to result for determining fetal lung maturity for the Lamellar Body Count method and the Fetal Lung Maturity II. Our hypothesis is that the time to result will be significantly less using the Lamellar Body Count method, and the cost associated with this method over the traditional FLM II will be favorable.

NCT ID: NCT00611065 Withdrawn - Prostate Lesions Clinical Trials

Imaging of Prostate Cancer Using Two-dimensional MR Spectroscopy and Diffusion Tensor Imaging

Start date: June 2007
Phase: N/A
Study type: Interventional

The goal is to develop MR imaging techniques to improve delineation of cancer extent, and to improve differential diagnosis between prostate cancer and benign prostate hyperplasia or other benign diseases.

NCT ID: NCT00611013 Withdrawn - Healthy Clinical Trials

Magnetic Resonance Imaging and Spectroscopy at High Field

Start date: June 2002
Phase: N/A
Study type: Interventional

Evaluating novel MR imaging techniques on volunteers.

NCT ID: NCT00610831 Withdrawn - Breast Cancer Clinical Trials

Computed Radiography (CR) Data Collection for Mammography Computer Aided Detection (CAD)

Start date: May 2007
Phase: N/A
Study type: Interventional

The objective of this study is to collect an image library of diagnostic digital mammograms using the Carestream CR mammography system from patients who have histological-conformed breast cancer to demonstrate the clinical feasibility of this system for detection of breast cancer.

NCT ID: NCT00610805 Withdrawn - Clinical trials for Systemic Lupus Erythematosus

Cardiology Prevention in Systemic Lupus Erythematosus (SLE)

Start date: November 2009
Phase: N/A
Study type: Interventional

We propose a feasibility study of aggressive CV risk factor management directed by preventive cardiology compared to usual care. We will determine: 1) the efficacy of a preventive cardiology program compared to usual care in slowing the progression of carotid IMT and plaque, and 2) the effect of a preventive cardiology program versus usual care at achieving CV risk factor target goals. We hypothesize Lupus patients randomized to the preventive cardiology program will have less cardiovascular progression over two years than those lupus patients who are given standard care for cardiovascular risk, defined by carotid intima-media thickness and plaque.

NCT ID: NCT00610298 Withdrawn - Clinical trials for Neuromuscular Deficits

Effects of Whole Body Vibration in Elderly Patients Requiring Rehabilitation: A Pilot Study

Start date: October 2001
Phase: N/A
Study type: Interventional

The aim of this study is to accumulate data about the influence of whole body vibration on the functional recovery of adult patients with various neuromuscular and musculoskeletal deficits requiring physical medicine and rehabilitation treatments.