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NCT ID: NCT00141128 Completed - Clinical trials for Urinary Incontinence, Stress

Evaluation Of A Novel Methodology In The Assessment Of Urethral Function Using SS-RBX.

Start date: December 2005
Phase: Phase 2
Study type: Interventional

SS-RBX will be used to evaluate pharmacodynamic changes in urethral function using a novel methodology

NCT ID: NCT00140582 Completed - Follicular Lymphoma Clinical Trials

Primary Rituximab and Maintenance

Start date: December 2004
Phase: Phase 3
Study type: Interventional

- Objectives - Primary objective: To evaluate in patients with advanced follicular lymphoma the benefit of maintenance therapy with rituximab after induction of response with chemotherapy plus rituximab in comparison with no maintenance therapy - Secondary objective: To evaluate response rates, event driven survival endpoints (EFS, PFS, OS) and quality of life of four different chemotherapy regimens combined with rituximab, with or without maintenance with rituximab, for first line treatment of advanced stage follicular lymphoma. - Study Design This is an international open-label, multicentre, randomized study with two treatment phases. In the induction phase patients have to respond to 1st line induction treatment in order to be eligible for randomization to the second phase of maintenance treatment or observation. After the maintenance period patients will be included in the follow up phase for 3 years.

NCT ID: NCT00139945 Completed - Hypopituitarism Clinical Trials

Ghrelin, Growth Hormone and Cortisol Interaction in Growth Hormone Deficient Patients

Start date: October 2005
Phase: N/A
Study type: Interventional

In growth hormone deficient patients: Determination of endogenous circulating ghrelin levels, ghrelin effects on insulin sensitivity, appetite, energy metabolism, and signal transduction in fat and muscle.

NCT ID: NCT00139802 Completed - Clinical trials for Ischemic Heart Disease

DANish Multicenter STENT Trial

Start date: April 1997
Phase: Phase 4
Study type: Interventional

The purpose of the study was to evaluate procedural and late outcome of coronary artery stenting using 2 different unmounted stents

NCT ID: NCT00139178 Completed - HIV Clinical Trials

Switching From Zidovudine to an NNRTI or Lopinavir/Ritonavir in Patients Treated With Zidovudine/ Lamivudine/Abacavir.

Start date: March 2004
Phase: Phase 4
Study type: Interventional

Highly active antiretroviral therapy (HAART) has improved the long time survival of HIV infected individuals. However an increasing number of HIV-patients have developed metabolic and morphological alterations including peripheral lipoatrophy. The main hypothesis of the study is that switching from thymidine-analogue based HAART will reverse lipoatrophy. We plan to perform an observational study recruiting up to 100 HIV-infected patients receiving Trizivir (zidovudine/lamivudine/abacavir). The patients will be offered an NRTI or lopinavir/ritonavir instead of zidovudine or they can choose to continue with Trizivir. The main endpoint is changes in peripheral fat mass as determined by DEXA-scanning.

NCT ID: NCT00138905 Completed - Behavior Clinical Trials

Experimental Study of Mobile Base Station Related Radio-Frequency Electromagnetic Radiation

Start date: February 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study, is to investigate if low intensity electromagnetic radiation, can influence the cognitive performances and well being of healthy adolescents and adults. Furthermore, the purpose is to provide any special information about the subjects which can cause the possible reactions. Finally, the investigation will try to clarify if there is anything specific in the radiation signal that causes the effect

NCT ID: NCT00138853 Completed - Osteoarthritis Clinical Trials

A Roentgen Stereophotogrammetric Analysis on Migration of Knee Prostheses.

Ti-Tan
Start date: November 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the early migration of two uncemented total knee arthroplasties with different metal coating. Only the tibial prosthesis plateau varies. One is made out of tantalum and has two short pegs for fixation into the tibia while the other is covered by titanium fiber-mesh on the bone-near site and has 4 short pegs for screw fixation into the tibia.

NCT ID: NCT00136617 Completed - Alcoholism Clinical Trials

Outpatient Treatment of Alcohol Withdrawal Syndrome

Start date: August 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare a fixed-schedule therapy versus a symptom-triggered therapy for alcohol withdrawal syndrome in medical outpatients. Objectives: - Self-governance in monitoring AWS (alcohol withdrawal syndrome) symptoms and medication - Clinically controlled trial of two regimens for medical treatment of alcohol withdrawal syndrome - Outpatient treatment of alcohol withdrawal syndrome

NCT ID: NCT00135928 Completed - Clinical trials for Acute Myocardial Infarction

Stem Cells in Myocardial Infarction

Start date: May 2003
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to investigate the effect of treatment with granulocyte-colony stimulating factor (G-CSF) bone marrow stimulation on circulating stem cells' ability to develop new blood vessels in the myocardium after an acute myocardial infarction.

NCT ID: NCT00135850 Completed - Clinical trials for Ischemic Heart Disease

The Effect of Mobilized Stem Cell by G-CSF and VEGF Gene Therapy in Patients With Stable Severe Angina Pectoris

Start date: March 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study was to evaluate the mobilization of non-haematopoietic mesenchymal and haematopoietic stem cells from the bone marrow with granulocyte colony stimulating factor (G-CSF) treatment alone and in combination with vascular endothelial growth factor (VEGF) gene therapy in patients with severe chronic occlusive coronary artery disease.