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NCT ID: NCT00469404 Terminated - Healthy Clinical Trials

Single Dose Trial Comparing the Plasma Levels of Two Different Analgesic Transdermal Patch Formulations (Protocol ID 297307)

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

The purpose of this study is to determine whether the plasma levels of two different analgesic transdermal patch formulations lead to same plasma levels of the active ingredient after single dose application.

NCT ID: NCT00469053 Terminated - Healthy Clinical Trials

Multiple Dose Trial Comparing the Plasma Levels of Two Different Analgesic Transdermal Patch Formulations (Protocol ID: 855509)

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

The purpose of this study is to determine whether two different analgesic transdermal patch formulations lead to same plasma levels of active ingredient after multiple dose application.

NCT ID: NCT00461214 Terminated - Healthy Clinical Trials

General Surgery Training Outcomes Project

Start date: October 2006
Phase: N/A
Study type: Observational

The purpose of the General Surgery Training Outcomes Project: Evaluating the Impact of the Curriculum on General Surgery Resident Training and Evaluation is to analyze data collected as a normal course of the general surgery curriculum. The information collected is data readily available and routinely collected on all participants in the general surgery curriculum at NewYork Presbyterian Hospital/Columbia Campus. This information may lead to improvement in the general surgery curriculum.

NCT ID: NCT00459693 Terminated - Healthy Clinical Trials

PET Evaluation of Brain Peripheral Benzodiazepine Receptors Using [11C]PBR28 in HIV-Seropositive Patients With (MCMD)

Start date: April 9, 2007
Phase: N/A
Study type: Interventional

The purpose of this protocol is to measure a receptor in the brain using positron emission tomography (PET) that is involved in inflammation.

NCT ID: NCT00453297 Terminated - Healthy Clinical Trials

Phase I Study to Evaluate the Safety and Efficacy of MF101 as Well as the Pharmacokinetics of Its Key Active Components

Start date: October 2006
Phase: Phase 1
Study type: Interventional

This Phase I trial in healthy, post-menopausal women is designed as a double-blind, placebo-controlled, randomized, ascending single-dose safety trial. MF101 will be administered as a single oral dose to a total of 32 enrolled subjects between the ages of 40-65 years. Eight subjects will be assigned to each of four cohorts. Within each cohort, six subjects will be randomized to receive MF101 and two subjects will receive placebo. MF101 doses will be incrementally escalated until the stopping criteria are reached. If stopping criteria are reached before the fourth cohort receives dosing, the next cohort may receive a dose between the dose that was administered to the cohort exhibiting symptoms of MF101 toxicity and the next lower dose group.

NCT ID: NCT00452647 Terminated - Healthy Clinical Trials

Comparison of Blood Pressure Throughout Pregnancy

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

The purpose of this study is to observe and analyze variation of diastolic blood pressure measurements at third trimester of pregnancy and when they present for delivery in comparison to healthy volunteers. When patients present for delivery, we expect blood pressure to be lower than normal. However this is not the case. We aim to determine where this trend occurs throughout to duration of pregnancy, and propose possible explanation as to the source of this event. After discharge, the information recorded includes each patient's blood pressure upon admission to the labor floor, and several blood pressure measurements from prior clinical visits.

NCT ID: NCT00420706 Terminated - Healthy Clinical Trials

Study Evaluating SCA-136 Tolerability With Dose Titration and Food

Start date: December 2006
Phase: Phase 1
Study type: Interventional

To evaluate whether the tolerability of SCA-136 is improved by dosing with food or by increasing dose amounts in a step-wise fashion.

NCT ID: NCT00410995 Terminated - Healthy Clinical Trials

Effects of Naproxen on Physical Performance

Start date: May 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of daily use of Naproxen (a commonly used over-the-counter NSAID) on the physical performance of athletes, as measured by maximum oxygen consumption.

NCT ID: NCT00409110 Terminated - Healthy Clinical Trials

Ocular Pulse Amplitude And Choroidal Laser Doppler Flowmetry

Start date: January 2006
Phase: N/A
Study type: Observational

This study intends to investigate the relationship between choroidal blood flow and ocular pulse amplitude (OPA).

NCT ID: NCT00400452 Terminated - Healthy Clinical Trials

Manual Wheelchair Skills Training for Long-term-care Residents

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

It is hypothesized that, compared to a control group, manual wheelchair users and their caregivers in the long-term-care setting who receive the wheelchair skills training program will improve their wheelchair skills to a statistically significant extent and will retain these improvements for at least one month.