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NCT ID: NCT02277366 Terminated - Lung Neoplasms Clinical Trials

Role of Bronchoscopy in Early Lung Cancer Screening of High Risk Population

Start date: May 2015
Phase: N/A
Study type: Observational

The purpose of this study is to determine the diagnostic yield of early lung cancer in high risk population, who smokes or has other risk factors, by different bronchoscopy,. Furthermore, another purpose is to determine whether the different bronchoscopy are significant different in diagnosing early lung cancer.

NCT ID: NCT02277210 Terminated - Infertility Clinical Trials

Follicular Flushing in Patients With Suboptimal Responses

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

The aim of the present study is to determine the effect of follicular flushing on the ongoing pregnancy rate in patients who developed four or fewer follicles of 14mm following standard ovarian stimulation for IVF.

NCT ID: NCT02268201 Terminated - Clinical trials for Kidney Transplant Recipients

A Study to Evaluate the Efficacy and Safety in Kidney Transplant Recipients When Changed From Cyclosporine to Tacrolimus Prolonged-release Capsule or Tacrolimus Capsule

Start date: July 23, 2013
Phase: Phase 4
Study type: Interventional

KTx recipients receiving cyclosporine-based immunosuppressive therapy, and in the opinion of the investigator would benefit from switch to a tacrolimus-based immunosuppression, will switch the immunosuppressive therapy to a tacrolimus-based one. Efficacy and safety of patients will be observed for 52 weeks.

NCT ID: NCT02267213 Terminated - Clinical trials for Hepatocellular Carcinoma

Efficacy and Safety Study of TLC388 to Advanced Hepatocellular Carcinoma

Start date: April 10, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of TLC388 (Lipotecan) as a second line treatment in subjects with advanced Hepatocellular Carcinoma.

NCT ID: NCT02240940 Terminated - Clinical trials for Ischemic Heart Failure

PARACHUTE China Approval Trial

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

The design of this study is a multi-center, prospective, single-arm clinical trial to evaluate the safety and efficacy of the Parachute percutaneous left ventricle partitioning system. The purpose of this trial is to use the Parachute percutaneous left ventricular partitioning system to isolate the malfunctioning portion of the left ventricle in patients with symptoms of heart failure due to ischemic heart disease and provide the data required to gain Chinese regulatory approval.

NCT ID: NCT02220088 Terminated - Clinical trials for Hepatocellular Carcinoma

The Efficacy and Safety of Retreatment With TAI for Patients Who Showed TACE-resistant: a Randomized Controlled Trial

Start date: December 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Transarterial chemoembolization (TACE) is considered the gold standard for treating intermediate-stage hepatocellular carcinoma (HCC). However, any treatment guidelines do not specify the criteria for repeating TACE. The study,conducted in Europe ,recently published in the journal of Hepatology shows the ART score of >=2.5 prior the second TACE identifies patients with a dismal prognosis who may not profit from further TACE sessions. However,in clinical practice,we also found some patients who showed TACE-resistant at the beginning of treatment may access to get objective response of retreatment with transcatheter arterial infusion (TAI). So the investigators conduct this prospective,randomized controlled study to find out whether the patient who showed TACE-resistant can obtain survival benefit from retreatment with TAI.

NCT ID: NCT02213692 Terminated - Hepatic Neoplasms Clinical Trials

Comparative Study on Liver Resection Between Harmonic Scalpel Versus Crush-clamping Method

Start date: May 2014
Phase: N/A
Study type: Observational [Patient Registry]

Blood loss during liver resection significantly associates with short term operative outcome. The median blood loss during partial liver resection is 700-1200ml in high-volume centers. Conventional method (crush-clamp) has been a standard technique for liver transection. Technique advances related to liver transection have contributed to reduction in blood loss. Several studies have showed that Harmonic Scalpel in liver resection is safe and easy to use. A nonrandomized study showed use of the Harmonic Scalpel was associated with decreased operative time, blood loss and transfusion requirement, and an increased incidence of postoperative bile leakage. However, no randomized study has compared the difference between liver resection using traditional technology and harmonic Scalpel. The objective of this prospective randomized study is to compare the safety and efficacy of liver resection using the harmonic scalpel device with the "crush-clamp" technique in respect to blood loss, liver transection time, hepatic hilum clamping time, hospital stay and postoperative complications.

NCT ID: NCT02183805 Terminated - Clinical trials for Carcinoma Breast Stage IV

Chemotherapy Followed by Peripheral Stem Cell Transplantation in Treating Metastatic Triple-negative Breast Cancer

Start date: June 17, 2014
Phase: Phase 2
Study type: Interventional

Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells.

NCT ID: NCT02164877 Terminated - Crohn's Disease Clinical Trials

Effect of Soluble Dietary Fiber on Bacterial Translocation in Crohn's Disease

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

The purpose of this study is to evaluate the effect of soluble dietary fiber on bacterial translocation and mucosal immunology in patients with Crohn's disease.

NCT ID: NCT02153840 Terminated - Plaque Psoriasis Clinical Trials

Clinical Trial of PSORI-CM01(YXBCM01) Granule to Treat Stable Plaque Psoriasis

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

The purpose of this study is to evaluate the efficacy and safety of Chinese herbal PSORI-CM01(YXBCM01) granule for stable plaque psoriasis, with blood stasis syndrome of Chinese Medicine.