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NCT ID: NCT00824759 Withdrawn - Healthy Clinical Trials

Cardioprotective Effects of Increased Endogenous Erythropoietin After Normobaric Oxygen Breathing

Start date: n/a
Phase: N/A
Study type: Interventional

Tissue hypoxia is the only accepted trigger for erythropoietin (EPO) production. However, in healthy subjects EPO concentrations have also increased after oxygen breathing. The aim of our study is to confirm these observations. Besides its main function in erythropoiesis, EPO has also shown tissue protective effects. The second goal of our study is to observe the cardioprotective effects of increased endogenous EPO, induced after normobaric oxygen breathing.

NCT ID: NCT00790257 Withdrawn - Clinical trials for Type 1 Diabetes Mellitus

Safety and Efficacy Study of Encapsulated Human Islets Allotransplantation to Treat Type 1 Diabetes

Start date: November 2008
Phase: Phase 1
Study type: Interventional

In view to avoid immunosuppression, the investigators are submitting a Phase 1 clinical trial protocol testing the safety and the efficacy of encapsulated human islets in a "Monolayer Cellular Device" for allogeneic islets transplantation in Type 1 diabetic patients performed at the University clinical hospital Saint-Luc, Brussels. Encapsulated human islets will be transplanted in the subcutaneous tissue as "safety procedure" for patients. This protocol (single center trial) is designed as a limited series of islets transplants for 15 Type 1 diabetic adult subjects.

NCT ID: NCT00752245 Withdrawn - Renal Failure Clinical Trials

Uremic Toxins in the Intensive Care Unit (ICU): Patients With Sepsis

Start date: July 31, 2008
Phase: N/A
Study type: Interventional

Study of the kinetics of uremic toxins in the ICU patients with acute renal failure, in order to optimize the dialysis dose: patients with sepsis/multi-organ failure. The sampling of blood and dialysate will be done during dialyses with different durations (4, 6 and 8h)

NCT ID: NCT00742807 Withdrawn - Pain Clinical Trials

Pain Evaluation During Follicle Aspiration: Comparison of Two Sedation Protocols

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

Giving infiltration analgesia around the neck of the womb (= paracervical block, PCB) is frequently experienced as a painful procedure by women undergoing follicle aspiration. Two sedation protocols, where in the one protocol a low dose of alfentanil hydrochloride is already administered before the PCB, will be compared with each other and pain relief measured using the 'Visual Analogue Scale' and the 'Short-Form McGill Questionnaire'

NCT ID: NCT00575302 Withdrawn - Infertility Clinical Trials

Study of Optimal Posology of Gonadotrophins in Patients With Insufficient Ovarian Response Due to Age

Start date: December 2007
Phase: Phase 4
Study type: Interventional

In In vitro fertilization (IVF) treatment, poor responder patients of more than 38 years old are randomized prospectively into two dosages of gonadotrophins. The outcome of treatment will be analyzed.

NCT ID: NCT00547326 Withdrawn - Clinical trials for Otitis Media With Effusion

The Effect of Osteopatic Cranial Techniques on the Audiometric and Tympanometric Values in Children Suffering From Otitis Media With Effusion.

Start date: n/a
Phase: N/A
Study type: Interventional

Children with otitis media with effusion will be treated with osteopatic cranial techniques or with a placebo treatment. Before and after the treatment audiometric and tympanometric measures will take place. This procedure will be repeated 3 times, once a week and every session will last for 30-45 minutes. The fourth week, only audiometry and tympanomtry will be done.

NCT ID: NCT00389753 Withdrawn - Hydration of Scars Clinical Trials

Aruba Aloë Formula F-BC-096 in the Treatment of Split Thickness Donor Sites After Wound Closure

Start date: n/a
Phase: N/A
Study type: Interventional

Comparison between use of Aruba Aloë formula F-BC-096 and control.

NCT ID: NCT00382837 Withdrawn - Clinical trials for Systemic Lupus Erythematosus

Study of Epratuzumab in Systemic Lupus Erythematosus

Start date: January 2007
Phase: Phase 3
Study type: Interventional

Epratuzumab is an investigational antibody designed to help treat SLE. The purpose is to evaluate safety and long term efficacy in concert with standard SLE treatments

NCT ID: NCT00375154 Withdrawn - Clinical trials for ARF Secondary to COPD Exacerbation

HERMES STUDY: Study on the Feasibility and Efficiency of Noninvasive Positive-Pressure Ventilation (NPPV) in Prehospital Care

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

The purpose of this study is determine if NPPV can be performed in a pre-hospital setting very early after onset of dyspnea with a similar benefit in need of intubation and mortality as in previous study in hospital context and if early NPPV intervention have a real, rather standard medical therapy, value, both on objectively measured parameters and on patient's clinical status.

NCT ID: NCT00313989 Withdrawn - Dental Implants Clinical Trials

Evaluation of Osseo-integration After Placement of Dental Implants With Patients Receiving Radiotherapy for Buccopharyngeal Oncology

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

Follow up of implants with patients receiving radiotherapy for buccopharyngeal oncology. Implants will be placed 6 weeks before start of the radiotherapy or at least 3 months after the end of the radiotherapy