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NCT ID: NCT00830934 Not yet recruiting - Pelvic Girdle Pain Clinical Trials

Trial for the Treatment of Pelvic and Back Pain in Pregnancy

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

The investigators aim to conduct a prospective open label randomized controlled trial to test the hypothesis that following initial assessment by a physiotherapist, group care exercise class is as effective in reducing pain as individual physiotherapy care.

NCT ID: NCT00845793 Not yet recruiting - Type 2 Diabetes Clinical Trials

The Meal Tray as a Tool and Platform to Change Eating Habits Among Hospitalized Diabetic Patients - An Intervention Study

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

This protocol is intended to test whether a focused nutritional intervention in hospitalized patients with type 2 diabetes can have an impact on long term eating habits, physical activity and anthropometric parameters. The rational is to use the food tray as a means of conveying simple and practical nutritonal and behavioral messages.

NCT ID: NCT00848666 Not yet recruiting - Tinea Pedis Clinical Trials

Safety and Efficacy of a Novel Topical Therapy for Tinea Pedis (Athlete's Foot)

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

The purpose of this study is to evaluate the safety and efficacy of a novel topical therapy in patients with laboratory confirmed tinea pedis. During the follow-up period clinical and mycological examinations will be performed.

NCT ID: NCT00849719 Not yet recruiting - Post Operative Pain Clinical Trials

Effects of a Combination of IV-PCA With Continuous IV Infusion of MO, Versus IV-PCA MO on Postoperative Pain

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

After major surgery, such as abdominal or thoracic surgery, the majority of patients experience moderate to severe pain that may not be optimally controlled. Inadequate pain relief may lead to complications that can hinder rehabilitation and slow recovery. Morphine (MO) is the most commonly used opioid for the treatment of post-surgical pain (14). The preferred method of administration nowadays is intravenous patient-controlled analgesia (PCA). In contrast, Continuous infusion of intravenous morphine (CIVM) is seldom used in Post-Anesthesia Care Units (PACUs) for acute postoperative pain, due to concerns of cardio-respiratory deterioration, even though different studies have found this technique of administration effective and safe (in terms of opioid-related symptoms.As part of our efforts to improve postoperative pain management in the Tel Aviv Sourasky Medical Center's PACU, we wish to determine if combining CIVM with IV PCA will be superior over IV PCA only for the treatment of postoperative pain following major abdominal or thoracic surgery.Our hypothesis is that the continuous infusion, even if given at a relatively low dose, would enable the build-up of pharmacologically effective MO blood level, thus providing an overall better control of pain.

NCT ID: NCT00850317 Not yet recruiting - Fanconi Anemia Clinical Trials

Fanconi Anemia Transplant Lacking Genotypically Identical Donor

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

A research study for patients with Fanconi Anemia whose bone marrow has changed and now failed, giving rise to a pre-leukemia or leukemia. This study is a Phase II clinical trial in which patients will undergo allogenic transplant of stem cells, meaning they will receive bone marrow cells from a healthy donor. The purpose of this study is to see if transplant course of treatment will lower the risk of graft vs. host disease.

NCT ID: NCT00854243 Not yet recruiting - Clinical trials for Rheumatoid Arthritis

Role of Greyscale and Power Doppler Sonography in Therapy Monitoring in Early Rheumatoid Arthritis (RA)

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

The purpose of this study is to evaluate the role of musculoskeletal ultrasound and power Doppler in early therapy monitoring of rheumatoid arthritis patients.

NCT ID: NCT00854529 Not yet recruiting - Bleb Vascularity Clinical Trials

Subconjunctival Bevacizumab Effect on Bleb Vascularity

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

Trabeculectomy is an ocular surgery intended to reduce intra-ocular pressure the surgery creates a sub-conjunctival filtering bleb which filters aqueous humor fluid out. A rather common adverse event of the surgery is increasing vascularity of the conjunctiva overlying the bleb. This leads to adherence of the conjunctiva to the sclera and fibrosis and finally failure of the bleb (and of the surgery) this study intends to demonstrate that post operative subconjunctival bevacizumab injection will reduce incidence of bleb vascularity and ultimately, bleb failure.

NCT ID: NCT00854763 Not yet recruiting - Hypertension Clinical Trials

Olmesartan on Ambulatory Blood Pressure Change

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

We will conduct an open label, non-comparative, observational study to evaluate the efficacy, safety and tolerability of Olmesartan therapy in Taiwan patients with essential hypertension, and the primary objective is the change in the 24-hour mean systolic blood pressure from baseline to the day after post-treatment week-12 visit according to the ambulatory blood pressure monitoring.

NCT ID: NCT00855777 Not yet recruiting - Dental Extraction Clinical Trials

Etoricoxib Versus Ibuprofen in Third Molar Extraction Pain

Start date: April 2009
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the analgesic efficacy of etoricoxib compared with a well known and widely used non-steroid antinflammatory drug, ibuprofen, in third molar extraction pain. At this time, there are no data about the efficacy of etoricoxib for reducing pain following dental extraction. This will be a single center, randomized, double-blind study, in which patients with moderate to severe pain following third molar extraction will be randomized to receive etoricoxib (120 mg in a single dose + 2 dose of placebo pro day for 3 days) or ibuprofen (1800 mg in 3 doses pro day for 3 days). Paracetamol plus codeine will be used as rescue medication. Pain assessment will be performed using a 11-point pain intensity scale (0 = no pain and 10 = worster pain) during the first 3 days after dental extraction. Patients will be enrolled 15 days before the dental extraction. During enrollment visit a complete clinical evaluation with particular attention for potential exclusion criteria (e.g. hypertension and cardiovascular risk factors) as well as blood analyses will be performed. A follow-up visit will be performed 15 days after the dental extraction. Tolerability will be assessed through recording of adverse events.

NCT ID: NCT00857038 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Doxycycline and Airway Inflammation in Chronic Obstructive Pulmonary Disease (COPD)

Start date: April 2009
Phase: Phase 4
Study type: Interventional

COPD is a progressive pulmonary disease that is characterized by an inflammatory process in the airways and the lungs which leads to progressive airway obstruction. The inflammation is associated with tissue loss and remodelling. The investigators hypothesized that doxycycline reduces neutrophilic airway inflammation in patients with COPD. Therefore the investigators will conduct a randomized trial of doxycycline in 30 patients.