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NCT ID: NCT00382746 Withdrawn - Clinical trials for Congestive Heart Failure

EarlySense Monitoring Device Evaluation on CHF Patients

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

CHF patients will be monitored using EarlySense ES-16 device and will simultaneously fill diaries and log their weight daily. The data collected and analyzed by the ES-16 device will be correlated with the CHF status data.

NCT ID: NCT00376649 Withdrawn - Crohn's Disease Clinical Trials

Development of Workshop for Lifestyle Changing for Crohn's Disease Patients and Its Affect on the Disease's Indexes

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

Subjects that participate in the practical workshop will improve their quality of life and will stay longer in remmision , in compare to the participants that will continue their regular threatment

NCT ID: NCT00364975 Withdrawn - Breast Cancer Clinical Trials

Development of Gourmet Healthy Cooking Workshop for Cancer Patients

Start date: December 2006
Phase: N/A
Study type: Interventional

Subjects that participate in the practical workshop will improve their metabolic indexes, control their weight and improve their quality of life, in contrast to the participants that will take part in the nutritional consulting sessions

NCT ID: NCT00364338 Withdrawn - Perimenopausal Clinical Trials

Development of Gourmet Medical Cooking Workshop for Lifestyle Changing and Its Affect on Perimenopausal Women

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

Subjects that participate in the practical workshop will improve their metabolic indexes, decrease their weight and improve their quality of life, in contrast to the participants that will take part in the nutritional consulting sessions

NCT ID: NCT00362245 Withdrawn - Clinical trials for Post Traumatic Bacterial Meningitis

Amikacin Penetration Into the Cerebrospinal Fluid

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The limited available data precludes establishing an antibiotic regimen in patients suffering from bacterial meningitis after head trauma, or spontaneous bleeding Understanding the disposition of Amikacin administered intrathecally will enable to propose rational treatment of these patients.

NCT ID: NCT00362219 Withdrawn - Pain Clinical Trials

Topical Morphine for Analgesia in Patients With Skin Grafts

Start date: January 2022
Phase: Phase 3
Study type: Interventional

The management of pain endured by patients after skin grafting is complex. Pain is the single most distressing symptom but as it is difficult to manage, it is often under-treated. These patients may experience pain from two types of wound: the original injury and from "skin-donor" sites, areas of healthy skin from which skin is surgically removed and used to cover the original injury. As the section of skin which is removed is standardized, the wound created at the donor site is uniform and so provides a model of an acute wound. Opioids (such as morphine) are the backbone of treating the moderate to severe pain experienced by any patient. But due to their potentially severe side effects and that some patients do not experience sufficient relief from the treatment, optimal treatment schedules are still being sought after. Topically applied morphine has provided effective and safe analgesia in several clinical models. We, therefore, wish to apply this treatment modality onto skin-graft donor wounds. If found to be effective this could be an appealing non-invasive method to treat the pain of this type of wound.

NCT ID: NCT00361998 Withdrawn - Cystitis Clinical Trials

Nitrofurantoin Macrocrystals 3 Days Versus 7 Days in the Treatment of Women With Uncomplicated Cystitis

Start date: September 2006
Phase: Phase 4
Study type: Interventional

Our guidelines in the community recommend the use of NM for the treatment of women with community acquired UTI. While the length of treatment for uncomplicated cystitis with quinolones or TMP-SMX is three days, NM is recommended for seven days. However, there are not sufficient papers that establish the optimal length of treatment with NM in this population. The aim of this proposal is to evaluate and compare NM 3 day vs. 7 day treatment for the treatment of women with uncomplicated UTI.

NCT ID: NCT00361608 Withdrawn - Type I Diabetes Clinical Trials

Monitoring of Nocturnal Hypoglycemia Using EarlySense Monitoring Device

Start date: July 2008
Phase: N/A
Study type: Observational

This study observes the continuous measurement of breathing patterns, heart rate, restlessness, and tremor in sleep using the EarlySense ES 16 device as a tool in the management of hypoglycemia in pediatric type I diabetes patients.

NCT ID: NCT00361426 Withdrawn - COPD Patients Clinical Trials

EarlySense Monitoring Device Evaluation on COPD, CHF and Pneumonia Patients

Start date: January 2008
Phase: N/A
Study type: Observational

Continuous measurement of breathing patterns, heart rate, restlessness and cough in sleep using EarlySense ES 16 device. Predicting worsening in COPD patients' condition using the above parameters.

NCT ID: NCT00355420 Withdrawn - Fractures Clinical Trials

Evaluation of the Change in Length of the Leg in Children After Treatment of Femur Fractures.

Start date: October 2006
Phase: Phase 2
Study type: Observational

Femur fractures are a common injury in the Pediatric population. Despite their high incidence little do we know about the long term implications on the bones' length. Our main goal is to clarify this obscure issue by assessing the femoral and tibial length as determined by the fractures, measuring techniques and treatment modalities