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NCT ID: NCT00665795 Completed - Clinical trials for Dysthyroid Orbitopathy

Morphometric Analysis of Orbital Structures in Graves´ Orbitopathy

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

The purpose of this protocol is to study orbital structures in Graves´ Disease using multidetector computed tomography and color doppler imaging. Some changes in orbital structures detected by imaging exams could predict severity of the ocular Graves´disease. Thus the study could be useful in improve medical management of patients with Graves´ Disease.

NCT ID: NCT00665756 Active, not recruiting - Open Angle Glaucoma Clinical Trials

Comparison of Efficacy Between Silicone Ahmed Glaucoma Valves and Second Trabeculectomy in Glaucoma Patients

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

In the management of open angle glaucoma, frequently more then one procedure is necessary to control the intra ocular pressure. There is still no consensus whether this second intervention should be a second trabeculectomy or a shunt device. In the present study we compare a second trabeculectomy versus Ahmed silicone shunt device in open angle glaucoma patients with previous trabeculectomy without proper IOP control.

NCT ID: NCT00665639 Completed - Candidiasis, Oral Clinical Trials

Trial of Two Dosing Regimens of Micafungin Versus Caspofungin for the Treatment of Esophageal Candidiasis

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

To determine the efficacy and safety of daily doses of IV micafungin versus IV caspofungin for the treatment of esophageal candidiasis

NCT ID: NCT00665561 Completed - Clinical trials for Human Immunodeficiency Virus

Prospective Observational Epidemiologic Study of Maraviroc's Safety

POEM
Start date: March 31, 2008
Phase:
Study type: Observational

The study will assess if use of maraviroc along with an optimized background regimen of antiretroviral drugs in usual clinical practice is as safe as using only an optimized regimen of antiretroviral drugs.

NCT ID: NCT00664716 Completed - Clinical trials for Rheumatoid Arthritis

Assessment Of The Safety And Efficacy Of BG9924 In Rheumatoid Arthritis (RA) Participants

RESPOND
Start date: July 2007
Phase: Phase 2
Study type: Interventional

Safety and efficacy of BG9924 in RA participants that have had an inadequate response to disease-modifying anti-rheumatic drug (DMARD) therapy.

NCT ID: NCT00664573 Terminated - Clinical trials for Rheumatoid Arthritis

104RA204 Assessment of the Safety and Efficacy of BG9924 in Rheumatoid Arthritis (RA) Participants

RESPOND-EXT
Start date: November 2007
Phase: Phase 2
Study type: Interventional

To observe the long-term treatment with BG9924 when administered to participants with RA who previously participated in a Biogen Idec Study.

NCT ID: NCT00664430 Terminated - Clinical trials for Secondary Hyperparathyroidism

Efficacy and Safety of Paricalcitol on the Treatment of Secondary Hyperparathyroidism in Calcitriol Resistant Dialysis Subjects

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to evaluate the efficacy and safety of paricalcitol in participants with moderate to severe secondary hyperparathyroidism (SHPT) undergoing hemodialysis who are resistant to treatment with calcitriol.

NCT ID: NCT00664391 Completed - Hygiene Clinical Trials

Safety Dermatological Evaluation: Acceptability With Gynecological Follow up - Dermacyd Breeze

Start date: January 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate the safety of the gynecological formulation in normal and usual usage condition of Dermacyd Breeze.

NCT ID: NCT00663390 Completed - Hygiene Clinical Trials

Safety Dermatological Evaluation: Acceptability With Gynecological Follow up - Dermacyd Delicata Pocket BR

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

The purpose of this study is to demonstrate the safety of the gynecological formulation in normal and usual usage condition of Dermacyd Delicata Pocket.

NCT ID: NCT00663325 Completed - Hygiene Clinical Trials

Safety Dermatological Evaluation: Acceptability With Gynecological Follow up - Dermacyd Tina Gel Sweet Flower

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

The purpose of this study is to demonstrate the safety of the gynecological formulation in normal and usual usage condition of Dermacyd Tina Gel Sweet Flower.