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NCT ID: NCT00894335 Recruiting - Adrenal Tumors Clinical Trials

Anesthesia Management of Retroperitoneal Adrenalectomies

Start date: May 2008
Phase: N/A
Study type: Observational

This study is a prospective, perioperative evaluation of hemodynamic and respiratory parameters in patients undergoing retroperitoneoscopic adrenalectomies.

NCT ID: NCT00890253 Recruiting - Clinical trials for Liver Transplantation

Safety Study of Calcineurin-Inhibitor-Free Immunosuppression After Liver Transplantation

CILT
Start date: January 2010
Phase: Phase 2
Study type: Interventional

A prospective, non-randomized two stage monocentric phase II clinical trial to evaluate a de-novo calcineurin-inhibitor (CNI)-free immunosuppressive regimen based on induction therapy with anti-CD25 monoclonal anti-body (basiliximab), mycophenolic acid (MPA), and mammalian target of rapamycin (mTOR) - inhibition with everolimus to determine its safety and to investigate the preliminary efficacy in patients with impaired renal function at the time-point of liver transplantation (OLT) with regards to the incidence of steroid resistant acute rejection within the first 30 days after liver transplantation.

NCT ID: NCT00886912 Recruiting - Healthy Clinical Trials

Training in Hypoxia to Prevent Acute Mountain Sickness

Start date: June 2008
Phase: N/A
Study type: Interventional

Some studies suggest that high-altitude related illnesses - like acute mountain sickness - could be prevented by acclimatisation, reached at low altitude using training in simulated altitude. The purpose of this study is to determine whether training in hypoxia is suitable to prevent acute mountain sickness.

NCT ID: NCT00886327 Recruiting - Crohn's Disease Clinical Trials

Detecting Postoperative Recurrence in Crohn's Disease

Start date: May 2009
Phase: N/A
Study type: Observational

Up to ¾ of patients who have been diagnosed with Crohn's disease (CD) will have to undergo bowel resection during their lifetime despite modern medical therapies. Unfortunately, disease recurrence is common and endoscopic detection of recurring inflammation precedes clinical relapse. Endoscopic investigation is therefore recommended to manage these patients. This multi center, prospective study compares the conventional endoscopic method, ileo-colonoscopy to a new technique, i.e., colonic capsule endoscopy (CCE). CCE enables investigation of the small bowel and the large intestines by using a double-sided video camera with about 10 hours acquisition time. This study aims to evaluate the performance of CCE to detect postoperative recurrence of CD and detection rate of colonic and anastomotic recurrence is compared to ileo-colonoscopy. Proximal (small bowel) lesions are additionally recorded and impact on clinical management of the findings is accounted for. Moreover, safety aspects and influence of the findings on progress of the disease are monitored. All consecutive patients who are operated for CD in any of the participating study centers are eligible. Included are patients with segmental small bowel, ileocecal or segmental colonic resection. In some cases capsule retention has been reported at an average of 2-3% with CD patients at elevated risk. Therefore, patency capsule is performed before application of the video CCE to exclude bowel obstruction. Sample size estimation results in n = 70, requiring each 140 capsule endoscopes and 140 patency capsules for performance of postoperative screening (ca 4-8 weeks postoperatively) and detection of postoperative recurrence (ca 4-8 months postoperatively).

NCT ID: NCT00885716 Recruiting - Schizophrenia Clinical Trials

A Shared Decision Making Training for Inpatients With Schizophrenia

Start date: May 2009
Phase: N/A
Study type: Interventional

Patients suffering from schizophrenia who attend the communication skills program engage more deeply in therapeutic reasoning and treatment decisions. This results in stronger preferences to participate, greater perceived involvement and better long term adherence compared to patients who do not attend the training.

NCT ID: NCT00884364 Recruiting - Clinical trials for Hematological Malignancies

Exercise During Chemotherapy for Patients With Hematological Malignancies

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The trial will evaluate the effects of aerobic exercise in patients undergoing chemotherapy for the treatment of a hematological neoplastic disease.

NCT ID: NCT00884338 Recruiting - Fatigue Clinical Trials

Cognitive Function After Stem Cell Transplantation

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The trial will evaluate the effects of an exercise program on the physical and cognitive performance of patients with hematological neoplastic diseases after high dose chemotherapy with stem cell support.

NCT ID: NCT00883961 Recruiting - Clinical trials for Hematological Disease

Exercise Following Autologous Peripheral Blood Stem Cell Transplantation

Start date: December 2009
Phase: Phase 3
Study type: Interventional

The study evaluates the effects of a supervised exercise program on the physical performance, the mood and the complications of therapy in patients undergoing a high-dose chemotherapy followed by an autologous peripheral blood stem cell transplantation.

NCT ID: NCT00883714 Recruiting - Fatigue Clinical Trials

Exercise During the Allogeneic Stem Cell Transplantation

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The study will evaluate the effects of a structured endurance exercise program on the physical performance, the mood and the complications of patients with hematological malignancies undergoing a high-dose chemotherapy followed by an allogeneic peripheral blood stem cell transplantation.

NCT ID: NCT00883402 Recruiting - Carotid Stenosis Clinical Trials

Carotid Endarterectomy Versus Carotid Artery Stenting in Asymptomatic Patients

ACST-2
Start date: January 2008
Phase: N/A
Study type: Interventional

The trial randomise patients with asymptomatic carotid artery narrowing in whom prompt physical intervention is thought to be needed, but there there is still substantial uncertainty shared by patient and doctor about whether surgery or stenting is the more appropriate choice. The study is looking at immediate risks (within one month)and at long term benefits