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NCT ID: NCT00586170 Terminated - Clinical trials for Nonunion of Fracture of Fifth Metatarsal

A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatarsal Non-Union Fractures

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

The purpose of this study is to analyze the effect of PEMF in surgical reconstruction of 5th metatarsal non-union fractures.

NCT ID: NCT00585845 Terminated - Clinical trials for Carcinoma, Non-Small-Cell Lung

Study of Safety and Tolerability of Intravenous CRS-207 in Adults With Selected Advanced Solid Tumors Who Have Failed or Who Are Not Candidates for Standard Treatment

Start date: December 2007
Phase: Phase 1
Study type: Interventional

This clinical trial will evaluate the safety and tolerability of CRS 207 an investigational product that is a weakened form (attenuated) of Listeria monocytogenes, a type of bacteria that is commonly found in the environment. CRS-207 has been altered in the lab to reduce its ability to cause disease, while maintaining stimulation of the immune system. CRS 207 has also been genetically modified with recombinant DNA to release an antigen called Mesothelin. Because CRS 207 stimulates an immune response to Mesothelin and Mesothelin may be present at higher levels on tumor cells than on normal cells, this clinical trial will also examine if CRS 207 boosts the immune system in a way that targets certain types of cancer. The purpose of this first clinical trial with CRS-207 is to identify an appropriate dose of the investigation agent for later clinical studies and to explore safety when given to consenting adults with advanced cancer of the ovary or pancreas, non-small cell lung cancer, or advanced malignant epithelial mesothelioma. Immunological response to CRS-207 and tumor status of study participants will also be measured. Patients who choose to enter the study must meet all study entry criteria and must have previously failed standard treatment for their cancer. Qualifying study patients will be assigned to receive one of several dose levels of CRS-207. Each patient may receive up to 4 intravenous administrations (21 days apart) of CRS-207 at their assigned dose level.

NCT ID: NCT00585585 Terminated - Clinical trials for Recurrent Major Depressive Disorder With Atypical Features

Pilot Study of Betahistine Dihydrochloride in the Treatment of Major Depression With Atypical Features

Start date: July 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine a dose of the investigational drug betahistine dihydrochloride that is both well tolerated and potentially effective in treating the symptoms of atypical depression. Atypical depression is characterized by the ability of the person's mood to improve temporarily in response to positive events, as well as features such as increased appetite, increased sleep and severe fatigue.

NCT ID: NCT00585559 Terminated - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Acetaminophen in aSAH to Inhibit Lipid Peroxidation and Cerebral Vasospasm

Start date: April 2007
Phase: Phase 3
Study type: Interventional

The objective of this study is to determine whether acetaminophen (APAP), N-acetylcysteine (NAC), and APAP in combination with NAC will inhibit lipid peroxidation in aneurysmal subarachnoid hemorrhage (aSAH), utilizing F2-IsoPs as biomarkers for lipid peroxidation.

NCT ID: NCT00584779 Terminated - Clinical trials for PK Properties Of Gabapentin In Subjects With Impaired Renal Function

An Open Label Pharmacokinetic Study Of Gabapentin In Japanese Subjects With Renal Impairment Including Hemodialysis

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

To confirm the pharmacokinetics following administration of gabapentin to Japanese subjects with renal impairment, compare the results to Western study results and confirm the adaptive possibility of dose adjustment in US package insert to Japanese.

NCT ID: NCT00582855 Terminated - Clinical trials for Amnestic Mild Cognitive Impairment

Effect of AQW051 in Patients With Memory Impairment

Start date: December 2007
Phase: Phase 2
Study type: Interventional

This study will investigate AQW051 in patients with either mild Alzheimer's disease or amnestic mild cognitive impairment. The effect on cognitive impairment will be measure using validated computerized tests which measure cognitive function. This study will also explore the safety and tolerability of AQW051 in these patients.

NCT ID: NCT00582036 Terminated - Hyperglycemia Clinical Trials

Glucose Control In Hematopoetic Stem Cell Transplant

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

To determine whether intensive glucose control results in improved mortality and reduced hospital stay length by performing a randomized trial of intensive glucose management (blood glucose goal 110 mg/dl) using continuous IV insulin and glucose vs. non-intensive glucose management (goal 200 mg/dl)

NCT ID: NCT00581997 Terminated - Clinical trials for Pulmonary Fibrosis Secondary to Systemic Sclerosis

QAX576 in Patients With Pulmonary Fibrosis Secondary to Systemic Sclerosis

Start date: December 2007
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety, tolerability, and mechanism of action of multiple doses of QAX576 in patients with pulmonary fibrosis secondary to systemic sclerosis

NCT ID: NCT00581477 Terminated - Clinical trials for Orthostatic Hypotension

Treatment of Orthostatic Hypotension

Start date: January 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to try different medications in patients with low blood pressure and other problems with their involuntary (autonomic) nervous system. The pharmacological trials in this study will perhaps lead to more effective treatment. The protocol includes single dose trials, dose-selection trials, 5-day trials and chronic (approximately 2 months) trials, although only dose-selection trials were consistently performed and have results presented.

NCT ID: NCT00579371 Terminated - Clinical trials for Diabetes Mellitus, Type 1

Cadaveric Islet Transplantation in Patients With Insulin-Dependent Diabetes Mellitus

Start date: March 17, 2004
Phase: Phase 1/Phase 2
Study type: Interventional

We hypothesize that the following improvements to islet transplantation will increase the islet mass successfully isolated and allow for engraftment from a single pancreas. The improvements are: - Using Two-Layer method preservation to improve pancreas quality before islet isolation - Maintaining isolated islets in culture before transplantation - Using a steroid-free immunosuppression regimen - Transplanting the best combination of donor and recipient possible after human leukocyte antigens (HLA) screening and final crossmatching