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NCT ID: NCT01251705 Recruiting - Corneal Thickness Clinical Trials

Comparation of Different Devices to Measure Corneal Thickness

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

Comparison of different methods for measuring peoples corneal thickness

NCT ID: NCT01250106 Recruiting - Obesity Clinical Trials

Probiotics as a Novel Approach to Modulate Gut Hormone Secretion and Risk Factors of Type 2 Diabetes and Complications

Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators aim to test the hypothesis that Lactobacillus Reuteri-enriched microbiota improves insulin sensitivity and glucose tolerance in obese healthy and obese type 2 diabetes patients by improving gut hormone secretion and compare these findings to healthy lean subjects.

NCT ID: NCT01249638 Recruiting - Clinical trials for Colorectal Cancer Metastatic

Cap+Bev vs Cap+Iri+Bev 1st-line Therapy in mCRC

Start date: December 2010
Phase: Phase 3
Study type: Interventional

Patient with multiple metastases, not eligible for surgery, might not profit from intensive chemotherapy regimens. Therefore less intensive regimens focusing on survival and disease control may be a better choice for first line treatment. Therefore this study investigates the combination of capecitabine and bevacizumab versus the combination of capecitabine, bevacizumab and irinotecan. In case of progressive disease, the therapy in patients treated with capecitabine and bevacizumab is intensified by adding irinotecan. Primary endpoint is time-of-failure strategy (TFS) comparing both treatment arms.

NCT ID: NCT01245075 Recruiting - Addiction Clinical Trials

Deep Brain Stimulation of the Nucleus Accumbens as a Novel Treatment in Severe Opioid Addiction

NASA
Start date: January 2011
Phase: Phase 0
Study type: Interventional

The main objective of this study is to assess the efficacy of bilateral deep brain stimulation (DBS) of the Nucleus accumbens (NAc) as a novel treatment in severe opioid addiction. The included patients have been treated so far with a substitute in form of methadone. Our hypothesis is that bilateral DBS of the NAc will significantly reduce the craving for heroin and thus enable the patients to decrease their Levomethadone-dosage substantially.

NCT ID: NCT01244321 Recruiting - Clinical trials for End-stage Heart Failure Awaiting VAD Implantation

COVADIS Pilot Trial: COseal in Ventricular Assist DevIceS

COVADIS
Start date: December 2010
Phase: N/A
Study type: Observational

The objective of this controlled, non-randomized, single-center pilot study (CoSeal arm prospective)study is to evaluate the efficacy of the synthetic surgical hydrogel CoSeal® in the prevention of cardiac adhesion formation in patients submitted to VAD procedures.

NCT ID: NCT01242358 Recruiting - Clinical trials for In the Study the Value of Capnography for Avoiding Complications During Sedation for PEG is Evaluated.

Capnography During Percutaneous Endoscopic Gastrostomy (PEG)

PEG
Start date: June 2010
Phase: Phase 3
Study type: Interventional

In this randomized controlled trial the utility of capnography gets evaluated. Hypoxemia may occur during sedation with midazolam and propofol. Whether hypoxemia may be prevented by an additional capnographic monitoring is subject of the study.

NCT ID: NCT01231217 Recruiting - Crohn's Disease Clinical Trials

Green Tea in Crohn's Disease

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

The purpose of this study is to assess whether green tea or coffee influence the course and life quality of patients with mild to moderately active Crohn's disease.

NCT ID: NCT01229475 Recruiting - Atrial Fibrillation Clinical Trials

Stepwise Approach Versus Linear Ablation in Patients With Recurrence of Persistent Atrial Fibrillation

REDO-AF
Start date: October 2010
Phase: N/A
Study type: Interventional

Catheter ablation of persistent atrial fibrillation (AF) remains a challenging procedure. Even in experienced centres, repeat interventions are necessary in up to 70 of patients to achieve sinus rhythm at a long-term follow-up. While there is a consensus to perform pulmonary vein isolation (PVI) as a cornerstone for the ablation of paroxysmal and persistent AF ablation, different additional ablation strategies are used to achieve a modification of the substrate that perpetuates the arrhythmia: linear lesions (anterior and roof lines) or ablation of complex fractionated atrial electrograms (CFAE). In the stepwise approach PVI, CFAE ablation and/or LL are combined according to the presenting arrhythmia during procedure. The aim of the study is to determine whether there is a difference in terms of freedom from arrhythmia between a stepwise approach and a linear ablation for repeat procedure in patient with recurrence of persistent atrial fibrillation.

NCT ID: NCT01229306 Recruiting - Clinical trials for Paroxysmal Atrial Fibrillation

Repeat Ablation Procedure in Patients With Relapse of Atrial Fibrillation

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

Catheter ablation with isolation of the pulmonary veins has proven to be an effective treatment option in patients with paroxysmal atrial fibrillation. In patients who have a relapse of paroxysmal atrial fibrillation after one ablation procedure the investigators compare the reisolation of all pulmonary veins to reisolation plus an anterior left atrial line.

NCT ID: NCT01228487 Recruiting - Osteoarthritis Clinical Trials

Influence of Oxidative Dysbalance on Secondary Osteoarthritis

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

The important role of mechanical joint stress for the insert and progress of osteoarthritis (OA) is supported by recent studies. The degeneration of joint cartilage is caused either by unphysiological load of a healthy joint or physiological load of a damaged joint. The exact mechanisms leading from increased weight bearing and overuse to cartilage degeneration are mostly unknown. The hypothesis of the study is that parameters of oxidative stress in the joint synovial space reflect damages possibly leading to OA. These parameters correlate with parameters of oxidative stress in the peripheral blood. Aim of the study is the identification of such non- invasive obtainable biomarkers which represent the degenerative and regenerative changes in joint.