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NCT ID: NCT00425815 Withdrawn - Schizophrenia Clinical Trials

Org 24448 (Ampakine) for Cognitive Deficits in Schizophrenia

Start date: April 2009
Phase: Phase 2
Study type: Interventional

The TURNS is a National Institute of Mental Health (NIMH) funded contract for the evaluation of new compounds for the treatment of cognitive impairments in schizophrenia (HHSN 27820044 1003C; P.I.: Steve Marder, M.D.). Despite advances in the safety, tolerability, and effectiveness of antipsychotic medications for the treatment of schizophrenia, many patients continue to be plagued by impairments in social and work functioning. Persons with schizophrenia commonly show deficits in a number of areas of cognition that include impairments in attention, memory, and executive functioning (the ability and organize one's behavior). Importantly, a large body of literature now shows a link between cognition and community functioning in schizophrenia. It is believed that treatments that improve cognitive deficits may lead to improvements in work and social functioning. A promising approach to improve the community functioning of patients with schizophrenia is to develop new agents that treat the cognitive deficits of the illness. One type of pharmacological compound that has shown promise at improving cognition is a group of drugs called ampakines. These drugs are believed to improve the activity of a neurotransmitter system in the brain called the glutamate system. Increased activity of this system has been linked to improvements in cognitive functioning. The current study is an eight-week trial comparing two doses of the ampakine drug, Org 24448, that will be added to patients' current atypical antipsychotic medication. One hundred thirty-five patients with schizophrenia, drawn from seven sites, will participate in the study. Cognition will be measured using a variety of paper-and-pencil and computerized measures from the consensus-derived NIMH Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) cognitive battery. Psychiatric symptoms and the ability to perform community-based tasks of daily living will also be measured. Because previous trials with this drug and other similar drugs have detected lasting cognitive benefits, this trial will also repeat clinical assessments four weeks after completion of the study medication.

NCT ID: NCT00577343 Withdrawn - Clinical trials for Hospital Acquired MRSA

Hospital Acquired and Community Acquired MRSA in GI Lab

Start date: April 2009
Phase: N/A
Study type: Observational

Hospital acquired and community acquired methicillin resistant staph aureus (MRSA) has become an important health issue for in recent years. Up to two thirds of patients that are hospitalized may be colonized with MRSA. The prevalence in the community is also on the rise and affects the young and healthy. It is unclear what the true prevalence of MRSA is in our own hospital and outpatient setting. This information would be relevant to how healthcare staff adhere to contact and universal precautions. : The purpose of this study is to determine the prevalence of MRSA in patients that have gastrointestinal endoscopy and endoscopic ultrasound.

NCT ID: NCT00663715 Withdrawn - Sciatic Nerve AH Clinical Trials

Ultrasound Description of the Sciatic Nerve

Start date: April 2009
Phase: N/A
Study type: Observational

Sciatic nerve blocks are frequently used for anesthesia or analgesia for surgery of the lower legs. Currently, if ultrasound is used to find the sciatic nerve, the leg must be raised to locate the nerve with the ultrasound probe on the back of the thigh. In pediatric surgery, the patients are anesthetized (asleep) before the block is given. It is difficult for one person to administer the sciatic nerve block using this method. We would like to identify the sciatic nerve using ultrasound on the side of the thigh and its location to the adjacent structures.

NCT ID: NCT00678626 Withdrawn - Breast Cancer Clinical Trials

Phase 2 Trial Of CP-751,871 And Docetaxel In Advanced Breast Cancer

Start date: April 2009
Phase: Phase 2
Study type: Interventional

This study will assess the effectiveness of CP- 751,871 when given in combination with docetaxel to women with the first occurrence of advanced breast cancer disease. The effectiveness will be measured by progression-free survival duration. Patients will be followed for 2 years from the date of randomization.

NCT ID: NCT00723918 Withdrawn - Polyneuropathy Clinical Trials

Combination of an Investigational Cannabinoid and Methadone for HIV-associated Neuropathy

Start date: April 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of methadone alone and in combination with SAB378 for the treatment of painful HIV-associated neuropathy.

NCT ID: NCT00732147 Withdrawn - Type 2 Diabetes Clinical Trials

Effects of Pramlintide on Endogenous Production of Very-low-density-lipoprotein (VLDL)-Triglyceride and Glucose in the Post Prandial State in T2DM

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

Diabetes affects almost 21 million people in the United States. In this study we will test a drug called Pramlintide(Symlin), and see how it works to lower blood sugar and fat levels after a meal. Lowering high sugar levels and fat levels after a meal is very important in the prevention of the problems that persons with type 2 diabetes often encounter. Hypothesis is that Pramlintide will lower blood sugar and fat levels after a meal.

NCT ID: NCT00775749 Withdrawn - Clinical trials for Postoperative Nausea and Vomiting

Transdermal Nicotine in Female Patients at High Risk for Post Operative Nausea and/or Vomiting (PONV)

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

The purpose of this study is to see if the nicotine patch reduces post operative nausea and/or vomiting (PONV) among non-smoking patients who are at high risk of PONV.

NCT ID: NCT00785239 Withdrawn - Asthma Clinical Trials

CryoSpray Ablation(tm)Thoracic Patient Registry

Start date: April 2009
Phase: N/A
Study type: Observational

The purpose of this study is to create a patient registry to collect and analyze information on subjects treated with the CryoSpray Ablation™ System post-510K approval.

NCT ID: NCT00787488 Withdrawn - Ovarian Cancer Clinical Trials

Pilot Study of IV and IP Chemotherapy Plus Abdominal Hyperthermia for Ovarian Ca

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

This is a pilot study aimed to test the feasibility and safety of administering combination chemotherapy with paclitaxel (both intravenously and intraperitoneally) and cisplatin (intraperitoneally) plus whole abdominal hyperthermia every 3 weeks in the treatment of optimally debulked, advanced or recurrent ovarian, primary peritoneal, and fallopian tube cancer patients.

NCT ID: NCT00814437 Withdrawn - Infertility Clinical Trials

Physiological Role of KiSS-1/GPR54 System in the Human Ovary

001-KIS
Start date: April 2009
Phase: N/A
Study type: Observational

The aim of this project is to study the physiological role of the KiSS-1/GPR54 system in the granulosa cells of the human ovary.