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NCT ID: NCT01843621 Completed - Dengue Clinical Trials

A Phase I/II Trial of a Tetravalent Live Attenuated DEN Vaccine in Flavivirus Antibody Naive Children

Start date: February 2005
Phase: Phase 1/Phase 2
Study type: Interventional

One year follow-up on immunogenicity and safety of a booster dose of DEN vaccine administered approx. 1 year following the second dose

NCT ID: NCT01841918 Completed - Clinical trials for Influenza Due to Influenza A Virus Subtype H5N2

Safety and Immunogenicity of Live Attenuated Influenza H5N2

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate immune response and safety of live attenuated influenza H5 vaccine candidate strain A/17/turkey/Turkey/05/133 (H5N2) manufactured by GPO, Thailand in healthy Thais.

NCT ID: NCT01841866 Recruiting - Clinical trials for Post Operative Sore Throat After LMA Removal

Laryngeal Mask Airway Removal During Deep Anesthesia in Children

Start date: May 2013
Phase: N/A
Study type: Interventional

Laryngeal mask airway (LMA) is widely used in children.The appropriate time to remove laryngeal mask airway is still inconclusive.Sore throat is one of common complications after general anesthesia. Sometimes postoperative sore throat affects patients' satisfaction and daily activities. It can be correlated with dysphagia and may limit oral intake especially in children.The incidence of postoperative sore throat after laryngeal mask airway insertion varies from 5.8-34% in adult(13) and 17.5% in pediatric.Somehow, almost the studies of postoperative sore throat after laryngeal mask airway removal were done in awake state. Our study object to test that post operative sore throat after LMA removal in deep anesthetized children is lower than awake children.

NCT ID: NCT01838772 Completed - HIV Clinical Trials

HCV Treatment in HIV Co-Infected Patients in Asia

Start date: December 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the effectiveness and tolerability of hepatitis C virus (HCV) treatment in HIV co-infected patients in routine health care services in Asia through a pilot model of care for treatment of HCV in resource-limited settings.

NCT ID: NCT01838044 Terminated - Clinical trials for Chronic Low Back Pain With a Neuropathic Component

Efficacy and Safety Study of Celecoxib and Pregabalin Compared With Celecoxib Monotherapy, in Patients With Chronic Low Back Pain Having a Neuropathic Component

Start date: October 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if treatment with celecoxib and pregabalin together would prove to be more effective in relief of pain than treatment with celecoxib alone in people who have chronic low back pain with a probable neuropathic component.

NCT ID: NCT01836393 Completed - Knee Osteoarthritis Clinical Trials

Efficacy Study on Symptomatic Control of Patient With Knee Osteoarthritis Between 14% of Plai (Plaivana®) to Placebo Gels

OA knee Plai
Start date: January 2013
Phase: Phase 3
Study type: Interventional

To determine whether plai cream is effective in treating mild to moderate degrees of osteoarthritis of the knee in the elderly patient compared with placebo cream.

NCT ID: NCT01834274 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Comparison of Fasiglifam (TAK-875) With Sitagliptin When Used in Combination With Metformin in Patients With Type 2 Diabetes

Start date: June 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of fasiglifam (TAK-875) plus metformin compared with sitagliptin plus metformin on glycemic control over a 24-week Treatment Period.

NCT ID: NCT01833585 Completed - Atherosclerosis Clinical Trials

Treatment of Chronic Critical Limb Ischemia With G-CSF-mobilized Autologous Peripheral Blood Mononuclear Cells

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of G-CSF-mobilized autologous peripheral blood mononuclear cell injection to ischemic limbs of patients with critical limb ischemia.

NCT ID: NCT01831206 Completed - Bacterial Keratitis Clinical Trials

Collagen Cross-linking in Infectious Keratitis Trial

Start date: March 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of collagen cross-linking for treatment of infectious keratitis.

NCT ID: NCT01828099 Completed - Clinical trials for Non-Small Cell Lung Cancer

LDK378 Versus Chemotherapy in Previously Untreated Patients With ALK Rearranged Non-small Cell Lung Cancer

Start date: July 9, 2013
Phase: Phase 3
Study type: Interventional

The primary purpose of the study was to compare the antitumor activity of LDK378 versus reference chemotherapy. Patients in the chemotherapy arm were given the option to switch to LDK378 after confirmed progressive disease (PD), while also had the choice to continue with pemetrexed treatment.