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NCT ID: NCT02340221 Terminated - Breast Cancer Clinical Trials

A Study of Taselisib + Fulvestrant Versus Placebo + Fulvestrant in Participants With Advanced or Metastatic Breast Cancer Who Have Disease Recurrence or Progression During or After Aromatase Inhibitor Therapy

SANDPIPER
Start date: April 9, 2015
Phase: Phase 3
Study type: Interventional

This international, multicenter, randomized, double-blinded, placebo-controlled study is designed to compare the efficacy and safety of taselisib + fulvestrant with that of placebo + fulvestrant in postmenopausal women with estrogen receptor (ER)-positive, human epidermal growth factor receptor-2 (HER2)-negative, oncogene that encodes for phosphatidylinositol-4,5-bisphosphate 3-kinase (PIK3CA)-mutant, unresectable, locally advanced or metastatic breast cancer after recurrence or progression during or after an aromatase inhibitor (AI) therapy. There will be a 2:1 randomization to the taselisib arm versus the placebo arm. Enrollment will be enriched for participants with PIK3CA mutant tumors via central testing. The anticipated duration of the study is approximately 3.5 years.

NCT ID: NCT02336620 Completed - Sepsis Clinical Trials

Balanced Salt Solution VS. Normal Saline Solution in Septic Shock

Start date: December 2014
Phase: Phase 3
Study type: Interventional

The Purpose of this study is to determine the impact of balanced salt solution versus chloride rich solution on clinical outcomes in paediatric severe sepsis or septic shock

NCT ID: NCT02336100 Completed - Clinical trials for Gastroesophageal Reflux Disease

Diagnostic Value of Flexible Spectral Imaging Color Enhancement (FICE) Plus Probe-based Confocal Laser Endomicroscopy (pCLE) for Minimal Change Esophageal Reflux Disease (MERD) Diagnosis

Start date: June 2011
Phase: N/A
Study type: Interventional

Gastroesophageal reflux disease (GERD) patients without obvious mucosal break by endoscopy were examined by FICE, followed by confocal. Validity scores for MERD diagnosis were analyzed.

NCT ID: NCT02335398 Completed - Pain, Chronic Clinical Trials

Development and Evaluation of a Methadone Protocol for Severe Chronic Pain Management

Start date: July 2011
Phase: Phase 4
Study type: Interventional

Methadone is a synthetic mu opioid agonist that has been proved as clinically effective in pain management. However, methadone usage for pain control in Thailand has been limited because physicians are not familiar with its dosing and concern about the risk of drug accumulation and cardiac arrhythmia. Therefore, this prospective study was conducted to evaluate the efficacy and safety of a methadone protocol in Thai patients with severe chronic noncancer and cancer pain.

NCT ID: NCT02332733 Completed - Dengue Clinical Trials

Evaluating the Safety of and Immune Response to a Dengue Vaccine (TV003) in Healthy Adults, Adolescents, and Children in Thailand

Start date: November 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of and immune response to two doses of a dengue vaccine (TV003) given 6 months apart to healthy adults, adolescents, and children in Thailand.

NCT ID: NCT02331797 Completed - Clinical trials for Tympanic Membrane Perforation

Endoscopic Overlay Tympanoplasty for TM Perforation

Start date: December 2014
Phase: N/A
Study type: Interventional

Minimally invasive surgery is becoming more common in many surgical fields. The wide view of endoscope allows for minimally invasive transcanal approach instead of large postauricular opening. The investigators conduct this study to compared post operative pain score (by Visual Analogue Scales) between conventional microscope lateral placing tympanoplasty and endoscopic lateral placing tympanoplasty.

NCT ID: NCT02331043 Completed - Clinical trials for Hypercholesterolemia

Serum Cholesterol Reduction Efficacy of Biscuit With Plant Stanol Ester

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

Efficacy of plant stanols as esters on LDL-cholesterol reduction is well documented. LDL-cholesterol lowering efficacy of the ingredient in a biscuit (providing 2 g plant stanols as esters per day) is less well known.

NCT ID: NCT02328183 Recruiting - Hospital Infection Clinical Trials

Efficacy of Polymyxin B Against Infections Caused by Extensively Drug-resistant (XDR) Gram-Negative Bacteria

XDR
Start date: December 2014
Phase: Phase 4
Study type: Interventional

The objective of the study is to evaluate the efficacy of Polymyxin B for treatment Gram negative bacterial infection. The hypothesis of study is Polymyxin B would be the new antibacterial agents for Thai Gram negative infected patients in case of desirable outcomes and minimal side effects.

NCT ID: NCT02328170 Completed - Allergy Clinical Trials

Comparative Study of Specific IgE Levels to Common Foods and Aeroallergens Measured by EUROIMMUN Allergy and ImmunoCap

Start date: May 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine the correlation of specific IgE levels to common foods and aeroallergens measured by EUROIMMUN Allergy and ImmunoCap

NCT ID: NCT02326207 Terminated - Clinical trials for Pneumonia, Ventilator-Associated

Weekly Versus no Routine Ventilator Circuit Changes in NICU

Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine incidence of ventilator-associated pneumonia compared between weekly and no routine ventilator circuit changes in neonatal intensive care unit