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NCT ID: NCT01257373 Recruiting - Clinical trials for Coronary Artery Disease

Efficacy and Safety of Firebird 2 Stent in Treatment of Complex Coronary Lesions in Diabetes

Start date: April 2010
Phase: Phase 4
Study type: Observational

The goal of this study is to assess the long-term efficacy and safety of Firebird2 Cobalt-Chromium(CoCr)-alloyed sirolimus-eluting stent in treatment of complex lesions in diabetes.

NCT ID: NCT01258881 Recruiting - Ovarian Cancer Clinical Trials

Retrospective Study of Ovarian Cancer Patients With Brain Metastasis

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

Ovarian cancer, especially epithelial ovarian carcinoma, has the highest mortality rate among the gynecologic malignancies. The majority of patients with epithelial ovarian carcinoma are diagnosed at advanced stage which has the overall survival rates of only 19-30%. As the advance in the managements which prolonged the overall survival, metastatic lesion in rare location such as brain was noted in few patients of ovarian cancer in recent years. In the retrospective study, the investigators will review the medical records of the ovarian cancer patients with brain metastasis in the investigators hospital to investigate the incidence, clinical courses, optimal managements and possible prognostic factors in the rare condition.

NCT ID: NCT01262157 Recruiting - Clinical trials for Erectile Dysfunction

Low Intensity ShockWave Therapy for ED in Non Responders to PDE5i - a Double Blind Placebo Controlled Study

LI-ESWT
Start date: April 2010
Phase: Phase 3
Study type: Interventional

Low intensity shock waves (LISW) have been proven in animal studies to induce local growth of new blood vessels. The investigators hypothesized that LISW therapy could improve the symptoms of patients with erectile dysfunction resulting from a problem of blood supply that do not respond to oral therapy (PDE-5 inhibitors).

NCT ID: NCT01267578 Recruiting - Esophageal Cancer Clinical Trials

Peptide Vaccination in Treating Patients With Esophageal Cancer (STF-II)

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

The purpose of this study is to evaluate overall survival and immunological monitoring for peptide vaccination therapy using novel cancer testis antigens (STF-II) for locally advanced, recurrent, or metastatic esophageal squamous cell carcinoma

NCT ID: NCT01275898 Recruiting - Clinical trials for Coparison of Two Cerebral Oximeters

Comparison of INVOS and FORE SIGHT Cerebral Oximeter

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

Cerebral oxygenation can be monitored using near infrared spectroscopy. Different devices are available to assess cerebral oxygenation noninvasively. Beach chair position is assumed to influence cerebral oxygenation. Litte is known about the influence of prone position and head down position on cerebral oxygenation. The investigators hypothesize that these positions influence cerebral oxygenation. Further the investigators presume that the two cerebral oximeters INVOS and ForeSight provide comparable oxygenation data.

NCT ID: NCT01279499 Recruiting - Morbid Obesity Clinical Trials

Sevoflurane Versus Intravenous Anaesthetic Agents in Morbid Obese Patients

Start date: April 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of this prospective randomized clinical study was to compare anesthesia, in morbidly obese patents (BMI >50) who underwent BPD-RYGBP with either sevoflurane or propofol with remifentanyl.

NCT ID: NCT01298271 Recruiting - Liver Cirrhosis Clinical Trials

A Randomized Trial of GVS Alone vs. Propranolol

P-GVO
Start date: April 2010
Phase: Phase 4
Study type: Interventional

Design a randomized trial to compare the effect of endoscopic cyanoacrylate injection obliteration versus non-selective beta-blocker in the primary prevention of gastric variceal bleeding.

NCT ID: NCT01304875 Recruiting - Fabry Disease Clinical Trials

Pulmonary Disease and Exercise Tolerance in Boys With Fabry Disease

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

When to start children with Fabry disease on therapy is controversial because of its expense and inconvenience. Many Fabry children complain of exercise intolerance. In adults, the investigators have found decreased lung function and ability to exercise on a treadmill. Whether or not lung function and exercise capacity is abnormal in children is unknown. While lung function and exercise tests are commonly part of routine evaluations for adults with Fabry, they are not yet for children. The objective of the proposed study is to more accurately define the lung and exercise abnormalities in a group of 20 boys from 8-18 years of age with Fabry disease who have not been treated with enzyme replacement therapy (Fabrazyme).

NCT ID: NCT01312844 Recruiting - Depression Clinical Trials

A Study of the Use of IV Scopolamine to Augment the Efficacy of Electroconvulsive Therapy (ECT)

Start date: April 2010
Phase: N/A
Study type: Interventional

The primary purpose of this study is to assess the ability of scopolamine to improve the antidepressant effects of ECT and to determine whether scopolamine will shorten the time to response and remission for patients receiving ECT. The hypothesis are: 1. Patients receiving ECT plus scopolamine will have greater improvement in depression symptoms than those receiving ECT plus placebo. 2. Patients receiving scopolamine in addition to ECT will require fewer ECT treatments to obtain response/remission compared to the group receiving ECT plus placebo. 3. Time to response and to remission in the scopolamine group will be significantly shorter compared to ECT alone.

NCT ID: NCT01317485 Recruiting - Clinical trials for Perforated Diverticulitis

Laparoscopic Peritoneal Lavage or Resection for Generalised Peritonitis for Perforated Diverticulitis

Ladies
Start date: April 2010
Phase: Phase 3
Study type: Interventional

The first objective (LOLA) of this integrated trial is to determine whether laparoscopic lavage leads to better clinical outcomes compared to sigmoidectomy in patients with perforated diverticulitis with purulent peritonitis in terms of mortality and major morbidity. The second objective (DIVA) is to determine whether sigmoidectomy with anastomosis or sigmoidectomy with end-colostomy is the superior approach in patients with perforated diverticulitis with either purulent or faecal peritonitis in terms of stoma free survival. The study is designed as a multicenter and randomised trial.