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NCT ID: NCT00811031 Withdrawn - Prostate Cancer Clinical Trials

Preoperative Docetaxel for Localized Progressive Castration-resistant Prostate Cancer (CRPC)

Start date: n/a
Phase: Phase 2
Study type: Interventional

Objectives: Primary: - To evaluate the association of the probability of increase in phosphorylation of platelet-derived growth factor receptor (PDGFR) of > 0.5 in peripheral blood leucocytes following pre-operative docetaxel chemotherapy, with progression-free survival in localized castration-resistant prostate cancer (CRPC) Secondary: - To evaluate the association of the probability of increase in phosphorylated platelet-derived growth factor receptor (PDGFR) expression in peripheral blood leucocytes > 0.5 with indices of tumor regression including PSA-decline by 50% and measures of objective regression of tumor by transrectal MRI following pre-operative docetaxel therapy. - Explore associations of probability of increase in phosphorylated PDGFR in peripheral blood leucocytes following pre-operative docetaxel therapy with plasma PDGF kinetics and spatial and quantitative PDGF and phosphorylated PDGFR expression in tumor and stromal compartments in resected specimens. - Evaluate the association of probability of increase in phosphorylated PDGFR expression in peripheral blood leucocytes following pre-operative docetaxel chemotherapy with overall survival outcomes. - Assess global quality of life measures at baseline and 6 and 12 months post-operatively. - Create a tissue archive comprising tumor and peripheral blood specimens as a suitable resource for future genomic and proteomic studies.

NCT ID: NCT00824759 Withdrawn - Healthy Clinical Trials

Cardioprotective Effects of Increased Endogenous Erythropoietin After Normobaric Oxygen Breathing

Start date: n/a
Phase: N/A
Study type: Interventional

Tissue hypoxia is the only accepted trigger for erythropoietin (EPO) production. However, in healthy subjects EPO concentrations have also increased after oxygen breathing. The aim of our study is to confirm these observations. Besides its main function in erythropoiesis, EPO has also shown tissue protective effects. The second goal of our study is to observe the cardioprotective effects of increased endogenous EPO, induced after normobaric oxygen breathing.

NCT ID: NCT00835887 Withdrawn - Clinical trials for End Stage Renal Disease

Relevance of Flavanols for Cardiovascular Function in End-Stage Renal Disease

ESRD
Start date: n/a
Phase: Phase 2
Study type: Interventional

In this study, the acute and long-term effects of flavanols on vascular function in patients with ESRD will be investigated.

NCT ID: NCT00846326 Withdrawn - Allergic Rhinitis Clinical Trials

Preventing Tolerance to Oxymetazoline in Allergic Rhinitis

Start date: n/a
Phase: Phase 4
Study type: Interventional

The investigators wish to evaluate the effects of decongestants like oxymetazoline and the lessening of this effect with time called 'tolerance'. The investigators will demonstrate a reversal of this tolerance with nasal steroids i.e. the investigators will show that nasal steroids protect against tolerance. This will tell us more on how the investigators can make this treatment effective and safe for patients suffering with allergic rhinitis.

NCT ID: NCT00849238 Withdrawn - Clinical trials for Primary Liver Transplant

Mycophenolate Mofetil Maintenance Therapy for Liver Transplantation

Start date: n/a
Phase: N/A
Study type: Interventional

The rationale for this study is to determine if Campath-1H can be used in liver transplant recipients to induce a state of immunological unresponsiveness that would not only eliminate the need for calcineurin inhibitors maintenance therapy, but also reduce corticosteroids utilization, decreasing the incidence of acute cellular rejection and perhaps reduce the severity of histologic recurrence of certain autoimmune diseases responsible for causing liver failure. The investigator propose a randomized prospective open label trial in 50 liver transplant recipients who will received a calcineurin inhibitors free immunosuppressive protocol that consist of a single dose of Campath-1H as an induction therapy in association with maintenance mycophenolate mofetil (CellCept®) and low dose steroids. The second group will receive a standard immunosuppressive regimen, which consists of IV steroid induction therapy and maintenance steroids, together with tacrolimus at a full therapeutic dose with no induction antibody therapy.

NCT ID: NCT00867841 Withdrawn - Pneumonia Clinical Trials

A Polymerase Chain Reaction (PCR) - Based Method to Improve Antibiotic Prescribing for Pneumonia

Start date: n/a
Phase: N/A
Study type: Observational

Pneumonia, or lung infection, is usually treated with antibiotics targeted against the organisms that the physician guesses are causing the problem. The determination of the exact cause of a patient's pneumonia is difficult. The problem is that the two major causes of community-acquired pneumonia are not easily distinguished on clinical grounds and are best treated by different antibiotics. The investigators hypothesize that antibiotic therapy can be targeted and improved by doing polymerase chain reaction (PCR) testing of nose swabs to identify probable implicated organisms and their antibiotic resistance patterns. This pilot study will be important to ensure that the laboratory testing is functional and that the emergency department-laboratory communication is optimal prior to doing a full-fledged randomized clinical trial.

NCT ID: NCT00874302 Withdrawn - Uterine Fibroids Clinical Trials

Safety and Efficacy of 25 and 50 mg Doses of Proellex® in Treating the Recurrence of Uterine Fibroid Symptoms

Start date: n/a
Phase: Phase 3
Study type: Interventional

Subjects with symptomatic uterine fibroids will be enrolled and will receive daily oral study medication for 4 months. This will be followed by a 6 month off-drug interval until there is a return of significant symptomatology. If they experience symptoms of a certain severity, the subject will enter a second 4 month treatment cycle and then a follow-up period.

NCT ID: NCT00879294 Withdrawn - Clinical trials for Perforated Appendicitis

The Effect of Gum Chewing on Postoperative Ileus

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to see if chewing gum after surgery for perforated appendicitis will shorten the time of intestinal dysfunction.

NCT ID: NCT00881413 Withdrawn - Peptic Ulcer Clinical Trials

Esomeprazole Versus Pantoprazole to Prevent Peptic Ulcer Rebleeding

Start date: n/a
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the clinical effectiveness of intravenous esomeprazole and pantoprazole in preventing recurrent bleeding in the patients with high-risk bleeding peptic ulcers after successful standard endoscopic hemostasis.

NCT ID: NCT00887055 Withdrawn - Heart Failure Clinical Trials

OPTIMA Bi-ventricular Capture Verification Study

Start date: n/a
Phase: Phase 4
Study type: Observational

The purpose of this study is to characterize the morphology (shape) of the intracardiac electrograms(EGM) from patients with a resynchronization therapy device.