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NCT ID: NCT00641745 Completed - Schizophrenia Clinical Trials

Lurasidone HCl - A Long Term Safety Phase 3 Study of Patients With Clinically Stable Schizophrenia

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

Lurasidone HCl is a compound being developed for the treatment of schizophrenia. This clinical study is designed to test the hypothesis that lurasidone is safe and tolerable long term among clinically stable patients. The study will also assess the long term effectiveness of lurasidone as compared to an active comparator.

NCT ID: NCT00641537 Completed - Clinical trials for Relapsing-Remitting Multiple Sclerosis

CLARITY Extension Study

Start date: February 29, 2008
Phase: Phase 3
Study type: Interventional

The purpose of this extension trial was to further evaluate the safety and tolerability of oral cladribine in subjects who have previously completed treatment within Trial 25643 (CLARITY). This trial also explored clinical benefit of prolonged 192-week versus 96-week treatment.

NCT ID: NCT00640432 Completed - Low Back Pain Clinical Trials

Safety And Efficacy Of Celecoxib Versus Sodium Diclofenac In The Treatment Of Acute Low Back Pain

Start date: October 2003
Phase: Phase 4
Study type: Interventional

To evaluate the safety and efficacy of celecoxib versus sodium diclofenac in subjects with acute low back pain

NCT ID: NCT00639977 Completed - Healthy Clinical Trials

Effect of Acupuncture on Intraocular Pressure

Start date: September 2007
Phase: Phase 1/Phase 2
Study type: Interventional

To evaluate the short-term effect of acupuncture on the intraocular pressure (IOP). Methods: A randomized controlled trial. Healthy volunteers will be randomly allocated to three groups: Acupuncture group - will be submitted to a 20-minute session of acupuncture with needles inserted in specific points (Tong Zi Liao, Yang Bai and Jing Ming); Sham group - will be submitted to a 20- minute session of acupuncture with needles inserted in false points located 1 cm from true points in areas without acupuncture's meridians; and Control group - no intervention. IOP measurement by a masked investigator using Goldmann applanation tonometry immediately before the intervention, as well as 30 minutes and 24 hours after the acupuncture.

NCT ID: NCT00639483 Completed - Schizophrenia Clinical Trials

Efficacy and Safety of Celecoxib as Add-on Therapy to Risperidone Versus Risperidone Alone in Patients With Schizophrenia

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

To assess the efficacy and safety of celecoxib as add-on therapy to risperidone versus risperidone alone in patients with schizophrenia

NCT ID: NCT00638924 Completed - Healthy Clinical Trials

Physiologic Variables in Healthy Women in Shuttle Walk Test

Start date: December 2007
Phase: N/A
Study type: Observational

To analyze the alterations of physiologic variables in healthy sedentary women in the Shuttle Walk Test, verify the distance reached and interruption causes of the test.

NCT ID: NCT00637377 Completed - Clinical trials for Macular Degeneration

Vascular Endothelial Growth Factor (VEGF) Trap-Eye: Investigation of Efficacy and Safety in Wet Age-Related Macular Degeneration (AMD)

VIEW 2
Start date: April 2008
Phase: Phase 3
Study type: Interventional

This study is a phase III, double-masked, randomized, study of the efficacy and safety of VEGF Trap-Eye in patients with neovascular age-related macular degeneration. Approximately 1200 patients will be randomized in Europe, Asia, Japan, Australia and South America.

NCT ID: NCT00636415 Completed - Analgesia Clinical Trials

Intra-Articular Morphine Versus Bupivacaine on Knee Motion in Patients With Osteoarthritis

Start date: June 2004
Phase: N/A
Study type: Interventional

CONTEXT AND OBJECTIVE: Osteoarthritis causes pain and disability in a high percentage of elderly people. The aim of the present study was to compare the analgesic effect of intra-articular bupivacaine and morphine in patients with knee osteoarthritis. DESIGN AND SETTING: A randomized and double-blind study was performed at a Pain Clinic of São Paulo Federal University. METHODS: Thirty-nine patients with pain for more than 3 months and an intensity higher than 3 on a numerical scale (zero to 10) were included. G1 patients received 1 mg (1 ml) morphine diluted in 9 ml saline by the intra-articular route, and G2 patients received 25 mg (10 ml) 0.25% bupivacaine without epinephrine. Pain was assessed on a numerical scale and knee flexion and extension angles were measured after administration of the drugs at rest and during movement. The total amount of analgesic complementation with 500 mg paracetamol was also determined.

NCT ID: NCT00635947 Completed - Pregnancy Clinical Trials

Study of Maternal Hydration on the Increase of Amniotic Fluid Index

Start date: July 1998
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of maternal hydration with oral isotonic solution and water on amniotic fluid (AF) index in women with normohydramnios.

NCT ID: NCT00635453 Completed - Clinical trials for Feeding and Eating Disorders of Childhood

Impact of the "Ten Steps for Healthy Feeding of Children Younger Than Two Years" in Health Centers

Start date: March 1, 2008
Phase: N/A
Study type: Interventional

A cluster randomized field trial to evaluate the impact that training healthcare workers in healthy feeding practices has on the nutrition and health of children.