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NCT ID: NCT00394641 Completed - Cerebral Palsy Clinical Trials

Impact of Listening to Low Tones on Motor Function in Children With CP

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

The study aims to evaluate the impact of a possible new treatment for hypertonia, contributing to the motor disability in children with cerebral palsy (CP). This study follows a 2005-2006 pilot study, that demonstrate a significant motor improvement in 4 children exposed to low tones via stereophonic Headphones.(A possible mechanism is a deep brain stimulation outspreading from the auditory pathways in certain tones) The goal of this study is to perform a double blind randomized placebo-controlled trial (RCT) on 30 children. A three-arm study, with one group receiving the proposed treatment-music with low tones and the other two groups receiving a placebo (music without tones or stories) will be performed. clinical and a non invasive laboratory measurements (surface EMG) related to spasticity, active and passive range of movement, isometric strength and upper and lower body function would be measured both before and after the treatment .the assessments will include also a Visual assessment , evaluation of gaze coordination and a quality of life and a caretaker burden questionnaires.

NCT ID: NCT00394797 Completed - Clinical trials for Moderate Ischemic Mitral Regurgitation

Surgical Correction of Moderate Ischemic Mitral Regurgitation

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

The purpose of this study is to try and determine whether repair of moderate ischemic mitral regurgitation at the time of coronary bypass graft surgery (CABG) has an impact on survival.We will compare patients undergoing CABG + mitral repair or CABG only groups. Primary endpoints include late survival. Secondary endpoints include event free survival, symptoms, and echocardiographic outcomes.

NCT ID: NCT00398736 Completed - Septic Shock Clinical Trials

A Non-invasive Approach to the Assessment of Volume Status in Mechanically Ventilated Septic Patients.

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

To evaluate the use of sonographic inferior caval vein assessment in mechanically ventilated septic patients. Volume assessment in mechanically ventilated patients with inflammation is of major importance to guide fluid therapy. The researchers investigated whether measurement of caval vein diameter correlates with invasively assessed volume-based hemodynamic parameters.

NCT ID: NCT00398788 Completed - Low Back Pain Clinical Trials

A Study on Efficacy (Effectiveness), Safety, and Impact on Quality of Life Measures of Dilaudid CR (Controlled Release);, Hydromorphone HCl in Patients With Chronic Low Back Pain

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

The purpose of the study was to characterize the safety, effectiveness, and impact on quality of life (QOL) measures of OROS® hydromorphone HCL in patients with chronic low back pain.

NCT ID: NCT00398957 Completed - Analgesia Clinical Trials

An Open-Label Evaluation of the Dose Proportionality of OROS� Hydromorphone HCL Tablets 8mg, 16mg, 32mg, 64mg

Start date: n/a
Phase: Phase 1
Study type: Interventional

The primary objective of this study was to examine the OROS® Hydromorphone HCL pharmacokinetic (the way a drug enters and leaves the blood and tissues over time) profile for dose proportionality after administration of 8mg, 16mg, 32mg and 64 mg tablets.

NCT ID: NCT00399048 Completed - Clinical trials for Osteoarthritis, Knee

An Effectiveness, Safety and Quality of Life Measures With Hydromorphone HCL, Dilaudid CR (Controlled Release)

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

The purpose of this study was to characterize the effectiveness and safety of OROS hydromorphone HCL and OxyContin in patients with chronic osteoarthritis (OA) of the knee or hip who are receiving chronic nonsteroidal anti-inflammatory drug (NSAID) or other nonsteroidal, non-opioid analgesic (ie, acetaminophen or aspirin) therapy.

NCT ID: NCT00399230 Completed - Dry Eye Clinical Trials

A Comparison of Optive in Patients Previously Using Systane for the Treatment of Dry Eye

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

To evaluate the effectiveness of NGT (Optive) vs. Systane Tears for patients with moderate to severe dry eye disease.

NCT ID: NCT00399295 Completed - Analgesia Clinical Trials

An Open-Label Evaluation of the Independent Effects of Coadministration of a High-Fat Meal and Naltrexone Blockade on the Pharmacokinetic Profile of Dilaudid OROS (Hydromorphone HCI) 16mg

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study was to compare the pharmacokinetic (the way a drug enters and leaves the blood and tissues over time) profile of Dilaudid OROS 16mg (Dilaudid Slow Release; hydromorphone HCL) administered under fasting conditions, following a high-fat breakfast meal. The study also examined the effect of naltrexone blockade on the pharmacokinetic profile of Dilaudid SR.

NCT ID: NCT00406510 Completed - Dry Eye Clinical Trials

Comparison of Frequency of Use of Optive and Systane

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

The purpose of this study is subjectively compare duration of action between Optive and Systane.

NCT ID: NCT00407017 Completed - Cataract Surgery Clinical Trials

Therapeutic Variables in Cataract Surgery

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

The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.