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NCT ID: NCT01012973 Completed - Clinical trials for Retinal Vein Occlusion

Vascular Endothelial Growth Factor (VEGF) Trap-Eye: Investigation of Efficacy and Safety in Central Retinal Vein Occlusion (CRVO)

GALILEO
Start date: October 2009
Phase: Phase 3
Study type: Interventional

To determine the efficacy of vascular endothelial growth factor (VEGF) Trap-Eye injected into the eye on vision function in subjects with macular edema as a consequence of central retinal vein occlusion

NCT ID: NCT01010828 Completed - Clinical trials for Gonarthrosis Patients Who Need Artificial Knee Joint Total Replacement

Review on Minimally Invasive Skin Incision in Vanguard PS Artificial Knee Joint System

Start date: October 1, 2009
Phase: N/A
Study type: Interventional

This study will show whether Tri-Vector method can ensure more extensive visual field and conduct the precise surgery when compared with Mini Mid-Vastus method by conducting 2 types of skin incision approach, Tri-Vector for 36 patients or Mini-Mid Vastus for 36 patients in Vanguard PS artificial knee joint total replacement observational period before and during surgery.

NCT ID: NCT01010763 Completed - Avascular Necrosis Clinical Trials

A Study on M2a Magnum Total Hip Arthroplasty

Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of this study includes the investigation of Metal-ion release and Renal Function analysis in M2a Total Hip Arthroplasty.

NCT ID: NCT01010022 Completed - Hemorrhage Clinical Trials

Trial of 6% HES130/0.4

Start date: November 2009
Phase: Phase 3
Study type: Interventional

The study shall evaluate the efficacy and safety of two different hydroxyethyl starch solutions (artificial colloids 6% HES130/0.4 and 6% HES70/0.5, Salinhes®) for intra-operative therapy of hypovolemia and maintenance of circulating blood volume in patients undergoing orthopedic surgery. The primary efficacy endpoint will be the required volume of colloid solution infused from start until end of surgery. It is the aim of the clinical trial to demonstrate that comparable volumes of colloid solution are used between treatment groups.

NCT ID: NCT01009658 Completed - Clinical trials for Gastroesophageal Reflux

MSG and Gastrointestinal Motility

Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to clarify the physiological function of sodium glutamate by measuring its effect on upper GI motility ( gastric emptying).

NCT ID: NCT01009593 Terminated - Neoplasms Clinical Trials

Efficacy and Tolerability of ABT-869 Versus Sorafenib in Advanced Hepatocellular Carcinoma (HCC)

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to assess the overall survival (OS) of oral linifanib given as monotherapy once daily (QD) compared to sorafenib given twice daily (BID) per standard of care in subjects with advanced or metastatic HCC.

NCT ID: NCT01008852 Completed - Clinical trials for Active Rheumatoid Arthritis

Study Evaluating The Efficacy And Safety Of SBI-087 In Seropositive Subjects With Active Rheumatoid Arthritis

Start date: December 2009
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the safety and efficacy of a dose and dosage regimen of SBI-087 in seropositive patients with active Rheumatoid Arthritis, who are on a stable dose of methotrexate.

NCT ID: NCT01008618 Completed - Chronic Pain Clinical Trials

A Confirmatory Study of Fentanyl in Participants With Osteoarthritis or Low Back Pain

Start date: January 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy and safety of fentanyl in opioid-naive participants with osteoarthritis (disorder, which is seen mostly in older persons, in which the joints become painful and stuff) or low back pain who cannot obtain a sufficient analgesic effect by the treatment of non-opioid analgesics (drug used to control pain).

NCT ID: NCT01008553 Completed - Postoperative Pain Clinical Trials

A Confirmatory Study of Fentanyl in Participants With Post-herpetic Neuralgia, Complex Regional Pain Syndrome or Postoperative Pain Syndrome

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

The purpose of this study is to evaluate the efficacy and safety of fentanyl in opioid-naive participants with post-herpetic neuralgia, complex regional pain syndrome or post-operative pain syndrome who cannot obtain a sufficient analgesic effect by the treatment of non-opioid analgesics (drug used to control pain).

NCT ID: NCT01008033 Completed - Onychomycosis Clinical Trials

Safety and Efficacy of Topical IDP-108 Versus Vehicle in Patients With Onychomycosis

Start date: November 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of topical application of IDP-108 versus vehicle in treating patients with onychomycosis.