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NCT ID: NCT01172626 Not yet recruiting - Epilepsy Clinical Trials

Exploration of Genotype Based Personalized Prescription of Valproate Sodium in Anti-epileptic Treatment

EGBPPVPA
Start date: August 2010
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the relationship between the side effects of valproate sodium in the treatment of epilepsy in Han Chinese and the genetic polymorphisms of drug metabolizing enzymes and pharmacokinetics of valproate sodium.

NCT ID: NCT01173952 Not yet recruiting - Quality of Life Clinical Trials

Quality of Life in Men Undergoing Robotic Assisted Laparoscopic Radical Prostatectomy Versus Radical Retropubic Prostatectomy

Start date: August 2010
Phase: N/A
Study type: Observational

This study is prospective evaluation of quality of life in men undergoing robotic assisted laparoscopic radical prostatectomy versus radical retropubic prostatectomy.

NCT ID: NCT01180088 Not yet recruiting - Liver Neoplasm Clinical Trials

Effectiveness of Routine Application Of Anterior Approach During Right Hepatectomy

AA
Start date: August 2010
Phase: N/A
Study type: Interventional

The aim of this study was to evaluated the advantages of routine application of the anterior approach in patients scheduled to right hepatectomy or extended right hepatectomy, without infiltration of segment 1, inferior vena cava or main bile duct.

NCT ID: NCT01180153 Not yet recruiting - Clinical trials for Biliary Tract Cancer

Study of S-1 Oxaliplatin (SOX) for Biliary Tract Cancer (BTC) (Ampullary Adenocarcinoma)

Start date: August 2010
Phase: Phase 2
Study type: Interventional

To evaluate efficacy and safety of S-1 Oxaliplatin (SOX) regimen to patients with unresectable, metastatic or locally advanced biliary tract or ampullary adenocarcinoma.

NCT ID: NCT01187290 Not yet recruiting - Clinical trials for Non-small Cell Lung Cancer

Preoperative Chemoradiotherapy Versus Chemotherapy Alone in Nonsmall Cell Lung Cancer (NSCLC) Patients With Mediastinal Lymph Node Metastases

Start date: August 2010
Phase: Phase 2
Study type: Interventional

The main objective of this trial is to compare feasibility and efficacy of sequential neoadjuvant chemoradiotherapy with 44Gy concomitant boost to neoadjuvant chemotherapy alone. Secondary objectives are to assess the value of position emission tomography (PET)in predicting pathological response and event-free survival(EFS)in stage IIIA non-small cell lung cancer (NSCLC). Further to compare the amount of serum DNA in patients with stage IIIa NSCLC before, during and after chemotherapy, before and after radiotherapy (in arm A) and during follow-up in patients randomized into the trial and to correlate the Deoxyribonucleic acid (DNA) variation with tumor response, remission duration and overall survival.

NCT ID: NCT01653613 Not yet recruiting - Leukemia Clinical Trials

Studying Genes in Samples From Younger Patients With Acute Lymphoblastic Leukemia

Start date: August 2010
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of blood and bone marrow from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors find better ways to treat cancer. PURPOSE: This laboratory study is looking into genes in samples from younger patients with acute lymphoblastic leukemia (ALL).

NCT ID: NCT01003171 Not yet recruiting - Healthy Clinical Trials

Pharmacokinetics of MCS in Healthy Volunteers

MCS-2-US-pk
Start date: August 2011
Phase: Phase 1
Study type: Interventional

This study is to examine the pharmacokinetics, absorption and serum concentrations of MCS and other components after once-daily oral dosing of MCS.

NCT ID: NCT01123044 Not yet recruiting - Eye Injury Clinical Trials

Transplantation of Cultivated Corneal Epithelial Sheet in Patients With Ocular Surface Disease

CLET
Start date: August 2011
Phase: Phase 3
Study type: Interventional

The aim of the study is to assess if transplantation of cultivated corneal epithelial stem cells could restore vision in patients with severe ocular surface disorder with a favourable safety profile that warrants further comparative study.

NCT ID: NCT01146626 Not yet recruiting - Hepatitis C Clinical Trials

Does Vitamin D Improves Sustained Virologic Response (SVR) in Genotype 2,3 Chronic Hepatitis C Patients?

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

Standard therapy for chronic hepatitis C virus (HCV) is (Peg/RBV) combination therapy obtaining sustained virologic response (SVR) in 80% of naïve patients with genotype 2,3. Studies rarely address the issues of improving host factors. The current study examines 1. whether adding vitamin D, a potent immunomodulator, could improve viral response and shorten treatment duration (from 24 weeks to 12 weeks) 2. whether Vitamin D levels predictes negative treatment outcome.

NCT ID: NCT01148277 Not yet recruiting - Liver Disease Clinical Trials

Propofol and Remifentanyl Versus Midazolam and Fentanyl for Diagnostic Colonoscopy in Patients With Compensated Cirrhosis Child A-B

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

This is a prospective, randomized-controlled trial (RCT) comparing the use of Propofol and Remifentanyl and traditional sedation (Midazolam and Fentanyl) for diagnostic colonoscopies in patients with compensated cirrhosis child A-B. The working hypothesis is that the use of propofol will be translated in a shorter recovery and discharge times with a higher patient satisfaction and a decrease in general complications (Hepatic Encephalopathy) in the context of patients with advanced liver disease.