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NCT ID: NCT00315783 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Comparison of Data Obtained by Echocardiography and Magnetic Resonance Imaging in Hypertrophic Cardiomyopathy

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

Compare data (structural and functional) obtained by transthoracic rest echocardiography and magnetic resonance imaging (with gadolinium) in 30 patients with hypertrophic cardiomyopathy

NCT ID: NCT00317057 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Outpatient Management of Patients With Exacerbation of Chronic Obstructive Pulmonary Disease

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

Patients admitted to the hospital with chronic obstructive pulmonary disease are evaluated with regard to early follow-up by a specialized nurse in the home after discharge.

NCT ID: NCT00317616 Recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

The Pre-symptomatic Familial Amyotrophic Lateral Sclerosis (Pre-fALS) Study

Pre-fALS
Start date: April 2006
Phase:
Study type: Observational

Pre-fALS is a prospective natural history and biomarker study of people not yet affected with ALS, but who are at genetic risk for developing ALS. The investigators aim to recruit unaffected (healthy) people from familial ALS (fALS) pedigrees in which a known genetic mutation associated with ALS has been identified; for this study, a fALS pedigree is one with two biologically related individuals who have or have had ALS and/or FTD. Individuals who may be at genetic risk for ALS and who belong to families with at least one affected family member who has tested positive for a known ALS genetic mutation may also be eligible to participate. Our goal is to study the pre-symptomatic phase, onset and progression of ALS and to learn more about genetic and environmental factors that put people at risk for developing ALS.

NCT ID: NCT00319007 Recruiting - Clinical trials for Adenomatous Polyposis Coli

Influence of Sulindac and Probiotics on the Development of Pouch Adenomas in Patients With Familial Adenomatous Polyposis

Start date: April 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether sulindac and VSL#3 - inulin, either combined or alone, are effective in treating or preventing adenoma development in the ileal anal pouch in patients with familial adenomatous polyposis.

NCT ID: NCT00330603 Recruiting - Clinical trials for Gastroesophageal Reflux

Serial Exhaled Breath pH Monitoring

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

This study will seek to determine the amount of acids a person with a chronic cough that is suspected to be related to acid reflux breathes out after coughing. The study will also seek to determine if this measurement can predict the best treatment for the cough. Subjects with a chronic cough which is suspected to be related to acid reflux for which their doctor has prescribed a proton pump inhibitor medication will be enrolled in this study.

NCT ID: NCT00334425 Recruiting - Infertility Clinical Trials

The Effect of LH-Priming During Early Follicular Phase in IVF Treatment.

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

To evaluate the effect of LH-activity supplementation during the early follicular phase in GnRHa down-regulated women undergoing IVF in terms of S-Estradiol levels on hCG day by comparing different combinations with HP-HMG and r-FSH.

NCT ID: NCT00338637 Recruiting - Multiple Sclerosis Clinical Trials

Measuring the Balance Improvement on Multiple Sclerosis Patients After a Short Training Period With an APOS (All Phase Of Step Cycle) Kit

Start date: April 2006
Phase: Phase 2
Study type: Interventional

Randomised double blind study of two parallel groups,one of the groups trained with the full APOS kit (a shoe with an additional bio mechanical device) The control group trained with the Apos shoe without the bio mechanical device. both groups will be checked at the beginning of the study, one month later and at the end of the study after two months. The tests include neurological test, functional test(FSST,up and go test and berg balance test) gate analysis and quality fo life (rays) test.

NCT ID: NCT00339001 Recruiting - Clinical trials for Retinopathy of Prematurity

Erythropoietin and Early Iron Supplement and Retinopathy of Prematurity

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

To evaluate the possibility that erythropoietin with early iron supplementation may induce retinopathy of prematurity or worsen this disease. In addition risk factors for the development of ROP will be checked.

NCT ID: NCT00364962 Recruiting - Clinical trials for Nasopharyngeal Carcinoma

Treatment Result of KTP Laser Nasopharyngectomy in Recurrent NPC Patients

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

Investigate the treatment result of KTP laser nasopharyngectomy in recurrent NPC patients

NCT ID: NCT00371904 Recruiting - Clinical trials for Kidney Transplantation

Trial of Rituximab Given Pre-Transplant to Sensitised Live Donor Kidney Recipients

RAPTURE
Start date: April 2006
Phase: Phase 2
Study type: Interventional

About one third of prospective kidney transplant recipients have antibodies in their blood directed against the tissues of their only available kidney donor. Recently, "desensitisation" treatments when administered pre-transplant have allowed successful transplantation of these patients despite high rates of acute antibody mediated rejection (AAMR). The investigators propose to test in a randomised controlled trial whether rituximab, a monoclonal antibody that depletes B-lymphocytes, will safely lower antibody mediated rejection (AMR) rates when added to "standard" therapy. The investigators will also test whether rituximab enables more patients to achieve a negative crossmatch against their donor and thereby allow more transplants to proceed.