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NCT ID: NCT00539448 Completed - Clinical trials for Diabetes Mellitus, Type 1

Gulf, Lantus, Apidra Evaluation in Type 1 Diabetics Study

GLANS
Start date: April 2007
Phase: Phase 4
Study type: Interventional

Primary objective : To evaluate the efficacy (in terms of change in HbA1c readings starting from baseline then after 13 weeks & at the end of the study which will be after 26 weeks) in subjects with type I diabetes mellitus. Secondary objective : - Recording the average daily dose of both insulin Glulisine & insulin Glargine in type I DM. - Recording adverse events.

NCT ID: NCT00504738 Completed - Asthma Clinical Trials

Lung Disease Collection (Qatar): Evaluation of the Lungs of Individuals With Lung Disease

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

The purpose of this protocol is to obtain biologic samples from the blood and lungs from patients with lung diseases in order to study the causes and indications of these disorders, learn how these lung disease manifest and progress, and how the lung disease can be treated.

NCT ID: NCT00504361 Completed - Asthma Clinical Trials

Blood Collection From Individuals With Lung Disease for Genetic Studies (Qatar)

Q-BC
Start date: May 2006
Phase: N/A
Study type: Observational

This is a research study where researchers are collecting blood to evaluate the genetic characteristics of individuals with chronic lung diseases, including asthma, COPD (chronic obstructive pulmonary disease), interstitial lung disease, cystic fibrosis, and lung cancer. The investigators hope to be able to identify an association between a genetic make-up in the blood samples and the risks of developing a particular lung disease, or severity of a lung disease. The findings of this study might be important to develop future preventative methods and potential treatments for the management of lung disease.

NCT ID: NCT00477373 Completed - Bipolar Disorder Clinical Trials

Gulf Evaluation of VAlproate (Depakine Chrono) in maNia Study

GEVANS
Start date: December 2006
Phase: Phase 4
Study type: Interventional

To assess the efficacy of Di-valproate in Bipolar I patients suffering from a manic episode according to DSM IV (APA 1994) over a 12 weeks period of treatment. To evaluate the clinical safety of Di-valproate.

NCT ID: NCT00433212 Completed - Clinical trials for Respiratory Insufficiency of Prematurity

Nasal Intermittent Positive Pressure Ventilation in Premature Infants (NIPPV)

NIPPV
Start date: April 2007
Phase: Phase 3
Study type: Interventional

The machines and oxygen used to help very premature babies breathe can have side-effects, such as bronchopulmonary dysplasia (BPD). Infants with BPD get more complications (a higher death rate, a longer time in intensive care and on assisted ventilation, more hospital readmissions in the first year of life, and more learning problems) than infants who do not develop BPD. Doctors try to remove the tube in the wind-pipe that links the baby to the breathing machine as soon as possible. However, small babies get tired, and still require help to breathe. One of the standard and common techniques to help them breathe without a tube in the wind-pipe is to use simple pressure support, nasal continuous positive airway pressure or nCPAP. This supports breathing a little, but it is often not enough to prevent the need to go back on the breathing machine. Nasal intermittent positive pressure ventilation (NIPPV) is similar to nCPAP, but also gives some breaths, or extra support, to babies through a small tube in the nose. NIPPV is safe and effective, and already in use as an alternate "standard" therapy. The main research question: After being weaned from the breathing machine, is NIPPV better than nCPAP in preventing BPD in premature babies weighing 999 grams or less at birth?

NCT ID: NCT00323648 Completed - Clinical trials for Uncomplicated Acute Cholecystitis

Does it Make Sense to Give Postoperative Antibiotics to Patients With an Uncomplicated Acute Cholecystitis

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

Each patient is preoperatively treated once profylactic with intraveneous antibiotics. Postoperatively, one group will be treated with intraveneous antibiotics during 5 days. The other group will receive no antibiotics.

NCT ID: NCT00247962 Completed - Clinical trials for Ankylosing Spondylitis

Study Evaluating Etanercept and Sulphasalazine in Ankylosing Spondylitis

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

The purpose of this study is to compare the efficacy of etanercept and sulphasalazine in the treatment of Ankylosing Spondylitis.