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NCT ID: NCT00600886 Active, not recruiting - Acromegaly Clinical Trials

Safety and Efficacy of Pasireotide Long Acting Release (LAR) vs. Octreotide LAR in Patients With Active Acromegaly

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The patients will receive either Pasireotide LAR or Octreotide LAR for one year of treatment. The objective of this study is to compare the proportion of patients with a reduction of mean GH level to <2.5 µg/L and the normalization of IGF-1 to within normal limits (age and sex related) between the two treatment groups (pasireotide LAR and octreotide LAR) at 12 months. Following one year of treatment patients may proceed into the study extension. Patients who did not respond to the treatment they were randomized to (based on month 12 assessment results) will be switched to the other treatment arm at month 13.

NCT ID: NCT00600860 Recruiting - Clinical trials for Myelodysplastic Syndromes (MDS)

A Prospective, Multicentre European Registry for Newly Diagnosed Patients With Myelodysplastic Syndromes

EUMDS
Start date: April 2008
Phase:
Study type: Observational

Study Objectives: To collect and describe demographics, disease-management, and treatment outcomes of Myelodysplastic Syndromes (MDS) patients who are newly diagnosed and classified according to the World Health Organization (WHO) criteria. To perform observational studies concerning relevant scientific research questions in MDS using clinical data and biological samples, and to present relevant research outcomes in the fields of diagnosis and prognostication, health related quality of life issues, health economics, and risk stratification for newly developed classes of drugs. To disseminate results of the studies to all stakeholders involved.

NCT ID: NCT00600418 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Identifying Toddlers and Their Parents Who Are Suffering From Posttraumatic Distress Following War and Terror

Start date: April 2007
Phase: Phase 0
Study type: Observational

The project is aimed at identifying children who are suffering from posttraumatic distress and increasing capacity to provide treatment for them and for their caretakers. The project will be implemented in 3 cities in Israel, Haifa, Kiryat Shmona and Sderot, exposed to terrorism and the effects of war

NCT ID: NCT00600379 Completed - Stroke Clinical Trials

Virtual Reality Training Program for Ambulatory Patients With Chronic Gait Deficits After Stroke

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the feasibility and efficacy of a virtual reality program for ambulatory patients with mild-to-moderate chronic gait deficits after stroke.

NCT ID: NCT00600340 Completed - Clinical trials for Metastatic Breast Cancer

2-arm Trial of Paclitaxel Plus Bevacizumab vs. Capecitabine Plus Bevacizumab

TURANDOT
Start date: April 2008
Phase: Phase 3
Study type: Interventional

First-line treatment of patients with locally recurrent or metastatic, HER2-negative breast cancer who have not received prior chemotherapy for locally recurrent or metastatic disease.

NCT ID: NCT00600093 Terminated - Parkinson Disease Clinical Trials

Perioperative Treatment of Parkinsonian Patients With Parenteral Amantadine

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether administrating of Amantadine (a dopamine agonist) to patients suffering from Parkinson disease during the perioperative period is safe, and to asses potential benefits of this treatment.

NCT ID: NCT00600054 Completed - Clinical trials for Recurrent Diffuse Pontine Gliomas

Phase 2 Study of Nimotuzumab in Pediatric Recurrent Diffuse Intrinsic Pontine Glioma

Start date: October 2007
Phase: Phase 2
Study type: Interventional

This is a phase 2, single-arm, multi-center study, with a safety review component, designed to evaluate the efficacy and safety of nimotuzumab in approximately 44 patients with recurrent diffuse intrinsic pontine glioma (DIPG) following one previous regimen for their disease. Patients must be diagnosed with radiologically verified recurrent diffuse intrinsic pontine glioma that is measurable in at least two dimensions. Patients are eligible without histologic confirmation. Treatment regimen will consist of two phases-induction and consolidation.

NCT ID: NCT00599898 Completed - Labor, Premature Clinical Trials

Nifedipine Compared to Atosiban for Treating Preterm Labor

Start date: January 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the efficacy and the safety of nifedipine compared to atosiban for treating preterm labor.

NCT ID: NCT00599742 Recruiting - Anxiety Clinical Trials

Comorbidity Between Balance and Childhood Anxiety

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

Previous studies report frequent comorbidity of anxiety and sensory-motor imbalance in adults (Sklare et al., 2001). Only a few studies tested the comorbidity in children. We confirmed that: a) children with primary diagnosis of poor balance demonstrate an elevated anxiety level (Brat et al., 2006, submitted) and, b) children with primary diagnosis of generalized anxiety disorder demonstrate poor balance performance (Erez et al., 2004). These studies demonstrate the presence of balance-anxiety comorbidity in children with primary disorder of either balance or anxiety. Our theoretical reasoning formalized under the "three stage theory of learning" points to the possibility that poor balance may either predispose or cause the emergence of anxiety disorder (Erez et al., 2004). Thus, in the present study we test two predictions: (a) high prevalence of comorbidity of anxiety and balance disorders in children with a primary diagnosis of generalized or separation anxiety disorder, and, (b) intensive balance training, but not training of flexibility and power, will reduce the level of anxiety in children with primary diagnosis of anxiety.

NCT ID: NCT00599729 Recruiting - Knee Osteoarthritis Clinical Trials

Measurement of Gait Spatio-Temporal Characteristics in Knee Osteoarthritis Patients

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

The purpose of the study is to evaluate the gait spatio-temporal parameters of patients with degenerative changes in the knee joint and to relate them with 2 questionares (WOMAC and SF-36).