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NCT ID: NCT00136565 Completed - Clinical trials for Peripheral T-cell Lymphoma

Study of Bortezomib Combined With ACVBP in Peripheral T-cell Lymphoma

Start date: January 8, 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy and the safety profile and toxicity of a combination of Velcadeā„¢ (bortezomib) with a standard chemotherapy regimen (ACVBP [doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone]) in the treatment of previously untreated patients with peripheral T-cell lymphoma (PTCL).

NCT ID: NCT00136552 Completed - Lymphoma Clinical Trials

Study for Newly Diagnosed Follicular Lymphoma Patients With a Large Tumor Burden

Start date: May 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess in a prospective multicentric study (Phase III) the introduction of a monoclonal antibody directed against B-cells associated with a standard therapy including chemotherapy and alpha-interferon in first line treatment of patients with a large tumor burden follicular lymphoma.

NCT ID: NCT00136344 Completed - Endophthalmitis Clinical Trials

Study of Antibiotic Prophylaxis for Endophthalmitis Following Cataract Surgery

Start date: September 2003
Phase: N/A
Study type: Interventional

Cataract is the most important cause of visual impairment and decreased mobility in the elderly. While surgery is usually successful, it is also responsible for permanent loss of vision in up to 0.1% of patients due to severe post-operative infection (endophthalmitis). Because of this risk, surgery is typically performed on one eye at a time leaving the patient with a monocular cataract causing considerable visual impairment with reduction in mobility and quality of life. A second operation is required which often takes place up to one year later. It is not known at present whether the post-operative complication of endophthalmitis can be prevented by perioperative use of antibiotics. This randomised study (masked and placebo-controlled for topical levofloxacin and unmasked for intracameral injection of cefuroxime) sets out to test in 4 groups, each of 8,750 cataract surgery patients, if either topical antibiotic (levofloxacin) perioperatively or an intraocular (intracameral) injection of antibiotic (cefuroxime) at the end of phacoemulsification cataract surgery or the combination provides effective prophylaxis of post-operative infection (endophthalmitis) compared to controls in whom perioperative antibiotics are not used. The result will provide a scientific basis for prophylaxis of infection (endophthalmitis) following cataract surgery in Europe as well as an accurate figure for the incidence of endophthalmitis following phacoemulsification cataract surgery in Europe for the first time.

NCT ID: NCT00136149 Completed - Dental Implants Clinical Trials

Study on Immediate Placement to Evaluate Astra Tech Osseospeed Implants in an Immediate Loading Protocol in Extraction Sockets and Healed Ridges

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

This is a study to evaluate immediate implants.

NCT ID: NCT00136136 Completed - Behavior Clinical Trials

Validation of Bispectral Index (BIS)-Monitor in 3 Groups of Newborn Children

Start date: August 1, 2003
Phase:
Study type: Observational

This study will evaluate the registration of the bispectral index and spectral edge frequency in relation to the behavioural state.

NCT ID: NCT00136123 Completed - Dental Implants Clinical Trials

Immediate Load of Dental Implants, Placed in Atrophic Upper and/or Lower Jaw of Partial or Complete Edentate Patients, According to Flapless Technique

Start date: December 1, 2005
Phase: N/A
Study type: Interventional

This study will evaluate the placement of implants with minimal invasive techniques. Immediately after the placement of the implants, functional loaded synthetic teeth will be placed.

NCT ID: NCT00135161 Completed - Clinical trials for Head and Neck Neoplasms

Feasibility Study of Incorporating 18F-FDG-PET Imaging in Radiotherapy for Head and Neck Cancer

Start date: September 2003
Phase: Phase 1
Study type: Interventional

The purpose of this trial is to study fluorodeoxyglucose-positron emission tomography (FDG-PET)-based dose escalation using intensity modulated radiation therapy (IMRT).

NCT ID: NCT00135148 Completed - Transsexualism Clinical Trials

Decrease of Libido of Post-Operative Male-Female Transsexuals and a Healthy Female Control Group

Start date: April 2004
Phase: N/A
Study type: Observational

Participants fill out a questionnaire on libido and their possible partner relationship. A blood sample is taken for sex steroid analysis.

NCT ID: NCT00134329 Completed - Diabetes Mellitus Clinical Trials

Erectile Dysfunction and Diabetes Mellitus

Start date: May 2005
Phase: N/A
Study type: Observational

This study consists of filling out a questionnaire on possible erectile dysfunction.

NCT ID: NCT00134303 Completed - Obesity Clinical Trials

Trial Comparing Metformin Versus Placebo in Non Alcoholic Steatohepatitis (NASH) Patients Receiving Bariatric Surgery for Obesity

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

This is a comparison of metformin versus placebo in NASH patients receiving bariatric surgery for obesity.