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NCT ID: NCT00748735 Completed - Heart Failure Clinical Trials

Left Ventricular Lead Position in Cardiac Resynchronization Therapy

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

Left ventricular (LV) lead position has crucial impact on cardiac resynchronization therapy (CRT) success. This study will compare fluoroscopy and myocardial deformation imaging for optimal definition of LV lead position.

NCT ID: NCT00750321 Completed - Clinical trials for Transcutaneous Electric Nerve Stimulation

Placebo Transcutaneous Electrical Nerve Stimulation (TENS)

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

Chronic musculoskeletal pain is a major problem in society. Treatments for people with musculoskeletal pain have limited efficacy. Transcutaneous Electrical Nerve Stimulation (TENS) is a commonly utilized, non-invasive treatment for pain that is a safe non-pharmacological treatment that has been utilized for treatment of musculoskeletal pain. Recent studies in animals in the PIs laboratory have begun to examine the mechanism of action of TENS. The current study is proposed to translate the findings from the animals to human subjects. One concern with TENS is that there is not an appropriate placebo. Since TENS delivers an electrical current through the skin to produce pain relief, patients can typically feel the stimulation under the electrodes. The standard placebo in prior clinical studies has been to utilize a unit that appears to be functioning (lights on) but does not deliver a current. In this case the subject would not feel the stimulation. We will compare this standard placebo to a new device in which a current is delivered for 30 seconds and then slowly ramps to off. This current would then be felt by the subject as intensity is set, and then would slowly ramp down. Thus, electrical currents will be felt by the subject. It is common for people to adapt to the TENS current so that they no longer feel the stimulation over time, or that the stimulation is felt at a lower intensity. This new placebo TENS would appear to mimic this event to the subjects. This new TENS would have the further advantage of being able to double-blind the study so that the therapist applying the treatment, and the subject receiving the treatment are unaware who is receiving the active treatment. The investigators will therefore test the adequacy of this placebo when compared to a standard placebo with no stimulation. Hypotheses: 1. TENS will reduce temporal summation and increase nociceptive threshold in normal subjects 2. Placebo TENS with a short burst of electrical stimulation will be considered by subjects to be an active TENS unit with a greater frequency than the standard TENS unit that does not produce electrical current 3. effectiveness of TENS will be associated with genotype of candidate pain genes (SNPs).

NCT ID: NCT00753818 Completed - Growth Clinical Trials

Developmental Effects of Infant Formula Supplemented With LCPUFA

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

The purpose of this study is to compare the effects on visual development, growth, cognitive development, tolerance, and blood chemistry parameters in term infants fed one of four study formulas containing various levels of DHA and ARA.

NCT ID: NCT00755066 Completed - Clinical trials for Seasonal Allergic Rhinitis

Effect of Intranasal Corticosteroids on Systemic Allergen Specific IgE

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

Evaluation of the effect of fluticasone propionate vs placebo applied as nasal spray on the increase of allergen-specific serum IgE levels following nasal exposure to recombinant allergens. Nasal sprays will be applied for four weeks starting two weeks before nasal provocation and serum IgE levels will be followed during eight weeks after nasal provocation.

NCT ID: NCT00756210 Completed - Obesity Clinical Trials

Lifestyle and Obesity

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

The objective of this trial is to determine the effect of different lifestyle interventions such as aerobic exercise and alternative resistance training methods, combined with a hypocaloric diet, on weight, body composition and metabolic risk factors in overweight and obese adults.

NCT ID: NCT00765531 Completed - Urolithiasis Clinical Trials

Stone Disease in Children and Their Families

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

The hypothesis of this study proposal is that pediatric urinary stone formers have genetic risk factors which predispose their urinary stone production. 50-60% of pediatric stone patients have a positive family history of urinary stone disease. Several genetic mutations have been identified which predispose patients to various types of urinary stones. These genetic mutations can also lead to other significant sequela besides stones, including osteopenia/osteoporosis (bone loss). Furthermore, metabolic abnormalities can be identified in more than 50% of pediatric stone formers, some of which can be improved and/or alleviated with medical intervention to help decrease rate of stone formation and the need for hospitalization and surgical intervention.

NCT ID: NCT00767286 Completed - Prostate Cancer Clinical Trials

Goserelin, Flutamine, and Radiation Therapy in Treating Patients With Locally Advanced Prostate Cancer

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

RATIONALE: Patient abstract not available PURPOSE: Patient abstract not available

NCT ID: NCT00771641 Completed - Clinical trials for Head and Neck Cancer

Fractionated Radiation Therapy in Treating Advanced Squamous Cell Carcinoma of the Head and Neck

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

RATIONALE: Patient abstract not available PURPOSE: Patient abstract not available

NCT ID: NCT00779298 Completed - Healthy Clinical Trials

Effect of Commercial Rye Whole-Meal Bread on Postprandial Blood Glucose and Gastric Emptying in Healthy Subjects

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

Increased intake of dietary fibre and whole grains is related to reduced risk of developing diabetes. The term "whole grain" is often used for whole-meal products in which the structure of the cereal grain is destroyed in the flour containing the original dietary fiber, but also for cereal products in which a large proportion of whole cereal grains is intact. The aim of this study was to evaluate the effect of commercial rye whole-meal bread (RWMB) compared to white-wheat bread (WWB) on gastric emptying rate (GER), postprandial glucose response in healthy subjects.

NCT ID: NCT00782860 Completed - Clinical trials for Early Pregnancy Failure

Early Pregnancy Failure: Factors Affecting Successful Medical Termination Treatment

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

The main purpose of our study was to which determine factors, those measured by ultrasound and also demographic and clinical factors (age, number of previous pregnancies, abortions and deliveries) predict outcome of medical treatment for early pregnancy failure. Our hypothesis was that gestational sac volume predicts outcome of medical treatment for early pregnancy failure.