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NCT ID: NCT01471262 Enrolling by invitation - Complications Clinical Trials

Right Hepatectomy in Patients Beyond 70 Years Old

Start date: January 2006
Phase: N/A
Study type: Observational

As a consequence of the increase in life expectancy, hepato-biliary surgeons have to deal with an emerging aged population, which has a potential higher risk for complication and worse long-term outcome. The investigators will be analyzing the liver function and outcome after right or extended right hepatectomy in patients over 70 years old.

NCT ID: NCT01467453 Enrolling by invitation - Glaucoma Clinical Trials

Clinical Application of Sensimed Triggerfish Sensor (TS) With Wireless Signal Transmission for Continuous Intraocular Pressure Measurement

Start date: November 2011
Phase: Phase 4
Study type: Observational

The study objective is to investigate the clinical applicability of continuous IOP measurement using TS with radio transmission over 24 hours. - Trial with medical device

NCT ID: NCT01467440 Enrolling by invitation - Glaucoma Clinical Trials

Efficacy of Selective Laser Trabeculoplasty in Patients Under Treatment With Topical Prostaglandines

Start date: November 2011
Phase: Phase 4
Study type: Observational

Retrospective analysis of efficacy of selective laser trabeculoplasty in patients under treatment with topical prostaglandins compared to patients without topical prostaglandins is performed. Inclusion criterion are patients with glaucoma or ocular hypertension, who underwent treatment with selective laser trabeculoplasty due to insufficient control of intraocular pressure during their routine treatment at the University Hospital Zurich / Division of Ophthalmology.

NCT ID: NCT01467388 Enrolling by invitation - Glaucoma Clinical Trials

Efficacy of Selective Laser Trabeculoplasty in Pseudophakic Patients

Start date: November 2011
Phase: N/A
Study type: Observational

Retrospective analysis of efficacy of selective laser trabeculoplasty in pseudophakic patients compared to phakic patients is performed. Inclusion criterion are patients with glaucoma or ocular hypertension who underwent treatment with selective laser trabeculoplasty due to insufficient control of intraocular pressure during their routine treatment at the University Hospital Zurich / Division of Ophthalmology.

NCT ID: NCT01325324 Enrolling by invitation - Clinical trials for Healthy Participants

Comparison of Different Portable Tonometers (Icare Pro, TONO-Pen AVIA, Perkins Tonometer, PASCAL Hand Held Dynamic Contour Tonometer)

Start date: March 2011
Phase: Phase 4
Study type: Interventional

In different cases intraocular pressure (IOP) have to measured in lying position. Therefore a lot of portable tonometers have been established. The Icare Pro is a new tonometer on the market that allows faster and more comfortable IOP-measurements. No local anesthesia is needed, what is a major advantage for the patients. In this study the investigators want to evaluate if IOP measurements with Icare Pro Tonometer are as reliable as they are with other established portable tonometers (Perkins, TONO-Pen and hand held-Dynamic Contour Tonometer). - Trial with medical device

NCT ID: NCT01302912 Enrolling by invitation - Clinical trials for Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma

Lymphoma in the Orbit

Start date: February 2011
Phase: Phase 4
Study type: Observational

Imaging techniques have considerably improved over the last decades and ocular adnexal lymphomas (OALs) nowadays can be detected. As major advances in immunophenotyping and molecular diagnostics in histology have been achieved offering an accurate diagnosis, the investigators would like to introduce that surgical biopsy of an orbital lymphoma becomes crucial for the possibility of a correct diagnosis and proper treatment. As radiotherapy accomplished great preciseness as well and OALs respond excellently to radiation, this therapy should be the treatment of choice in local defined lymphomas instead of blind treatment with steroids. Radiation results in great local control rates of 85% to 100% - Trial with surgical intervention

NCT ID: NCT01299233 Enrolling by invitation - Clinical trials for Glaucoma Patients and Healthy Controls

Reproducibility of RNFL Circle Scans With ART-Function of Heidelberg Spectralis SD-OCT Software Version 5.3

Start date: February 2011
Phase: Phase 4
Study type: Observational

To assess the improvement in reproducibility of 100 vs. 16 averaged images by Automatic Real Time (ART) using Spectralis™ Spectral Domain-Optical Coherence Tomography (SD-OCT, Heidelberg Engineering GmbH, Heidelberg, Germany) in retinal nerve fiber layer thickness (RNFL) circle scan-measurements. - Trial with medical device

NCT ID: NCT01293474 Enrolling by invitation - Clinical trials for Glaucoma Patients and Healthy Controls

Choroidal Thickness in Glaucoma Patients and Healthy Controls

Start date: February 2011
Phase: Phase 4
Study type: Observational

With the new software tool (EDI, enhanced depth imaging) of the Spectralis® spectral-domain optical coherence tomography (SD-OCT) it is possible to visualize and measure the choroidal thickness. In glaucoma a vascular component is known. Therefore a difference of choroidal thickness in glaucoma patients and healthy controls is proposed. - Trial with medical device

NCT ID: NCT01210781 Enrolling by invitation - Epilepsy Clinical Trials

Target Planning for Placement of DBS-electrodes and Follow-up of the Clinical Efficacy of Stimulation

Start date: September 2009
Phase:
Study type: Observational [Patient Registry]

Deep brain stimulation (DBS) has been established as therapy for severe forms of Parkinson's disease and other indications. A common target for stimulation is the subthalamic nucleus (STN). Nevertheless, there is no agreement on the mechanisms how DBS leads to clinical improvement. The project aims to describe the variability of target coordinates in the patient group and to relate it to clinical outcome as documented in standardized questionaires. - Trial with surgical intervention

NCT ID: NCT01150240 Enrolling by invitation - Clinical trials for Primary Immunodeficiency Disease

Clinical and Laboratory Online Patient- and Research Database for Primary Immunodeficiencies in Switzerland

Start date: October 2006
Phase: N/A
Study type: Observational

A Swiss national, multi-centre, online patient and research database will be created, using the existing ESID database server system. This database contains disease-specific data from patients with primary (inborn) immunodeficiency diseases (PID).