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NCT ID: NCT02125461 Completed - Clinical trials for Non-Small Cell Lung Cancer

A Global Study to Assess the Effects of MEDI4736 Following Concurrent Chemoradiation in Patients With Stage III Unresectable Non-Small Cell Lung Cancer

PACIFIC
Start date: May 7, 2014
Phase: Phase 3
Study type: Interventional

A Global Study to Assess the Effects of MEDI4736 following concurrent chemoradiation in Patients with Stage III Unresectable Non-Small Cell Lung Cancer.

NCT ID: NCT02123914 Completed - Allergic Rhinitis Clinical Trials

The Effect of Exercises on Physiological Changes and Clinical Symptoms in Allergic Rhinitis Patients

Start date: January 2012
Phase: N/A
Study type: Interventional

1. Moderate exercise training decrease cytokine response and rhinitis symptoms in patients with allergic rhinitis 2. Moderate exercise training combined with vitamin C supplementation decrease cytokine response and rhinitis symptoms in patients with allergic rhinitis 3. Moderate exercise training combined with vitamin C supplementation has more beneficial effects than moderate exercise training alone for decreasing cytokine response and rhinitis symptoms in patients with allergic rhinitis

NCT ID: NCT02123901 Completed - Type 2 Diabetes Clinical Trials

The Effect of Walking Meditation Training on Glycemic Control and Vascular Function in Patients With Type 2 Diabetes

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

Walking Meditation training would yield more favorable adaptations than walking alone in improving glycemic control and vascular function in patients with type 2 diabetes.

NCT ID: NCT02112656 Completed - Clinical trials for Hepatocellular Carcinoma

Study of ThermoDox With Standardized Radiofrequency Ablation (RFA) for Treatment of Hepatocellular Carcinoma (HCC)

OPTIMA
Start date: June 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether ThermoDox, a thermally sensitive liposomal doxorubicin, is effective in the treatment of non-resectable hepatocellular carcinoma when used in conjunction with standardized radiofrequency ablation (sRFA).

NCT ID: NCT02108327 Completed - Blood Loss Clinical Trials

Blood Loss Between Surgical Blade and Unipolar Electrocautery in TKA

TKA
Start date: April 2014
Phase: N/A
Study type: Interventional

Using of surgical blade may have less blood loss than unipolar electrocautery in Total Knee Arthroplasty (TKA).

NCT ID: NCT02108197 Completed - Clinical trials for Gestational Diabetes

Sleep Apnea and Gestational Diabetes

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

The investigators hypothesize that pregnant women with gestational diabetes will have a high incidence of sleep apnea, and that the treatment of sleep apnea will lead to improved glucose control in these women.

NCT ID: NCT02107911 Completed - HIV Clinical Trials

Factors Affecting the Intention to Take nPEP Among Thai MSM

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

The potential participants will be informed of the study details, including the study objectives. Once they have read the study information sheet and have a good understanding of the study, those who intend to participate in the study will be asked to sign the consent form for this study. There are 2 groups of participants: MSM who seek HIV voluntary counseling and testing service (phase I) and MSM who meet nPEP criteria (phase II).

NCT ID: NCT02106832 Completed - Bronchiectasis Clinical Trials

Ciprofloxacin Dry Powder for Inhalation (DPI) in Non-cystic Fibrosis Bronchiectasis (Non-CF BE)

RESPIRE 2
Start date: April 30, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate if the time to first pulmonary exacerbation of bronchiectasis or its frequency can be prolonged by inhalation of ciprofloxacin for 28 days every other 28 days or for 14 days every other 14 days over 48 weeks.

NCT ID: NCT02106793 Completed - Clinical trials for Chronic Rhinosinusitis

Mitomicin C for Prevention Postoperative Endoscopic Sinus Surgery Synechia and QOL in Chronic Rhinosinusitis

Start date: March 2015
Phase: Phase 3
Study type: Interventional

Primary objective - To compare the incidence of postoperative nasal synerchia between Mitomicin C and placebo in patients at 6 months after endoscopic sinus surgery - To validate the Thai version of disease-specific quality of life tool SNOT-22 Secondary objectives - To compare the clinical signs and symptoms of CRS in patients who receive Mitomicin C with those who receive placebo - To compare the disease-specific quality of life in patients who receive Mitomicin C with those who receive placebo - To compare the side effects of Mitomicin C versus placebo

NCT ID: NCT02106273 Completed - Clinical trials for One-lung Ventilation

The Use of LMA-Proseal and Endobronchial Blocker for One Lung Anesthesia, Case Series

Start date: April 2011
Phase: Phase 4
Study type: Observational

An observational pilot study to determine the success rate of using LMA Proseal in conjuction with endobronchial blocker to provide one-lung anesthesia for thoracic surgery.