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NCT ID: NCT03767673 Recruiting - Esophageal Atresia Clinical Trials

Cardiorespiratory Performance and Pulmonary Microbiome in Patients After Repair of Esophageal Atresia

Start date: August 10, 2017
Phase: N/A
Study type: Interventional

The majority of the clinical research on esophageal atresia focuses on the upper gastrointestinal tract. However, the trachea and the lung are also affected in many of these children, so that a lifelong pulmonary impairment may result. The importance of respiratory function in the context of follow-up of these patients has therefore been increasingly recognized in recent years. Scientific work has shown significantly, that patients following esophageal atresia repair develop respiratory symptoms more frequently than the normal population. Mild impairment of the pulmonary function in adolescence and adulthood was demonstrated in some studies, but to date, there is no exact idea about the relationship between early childhood disease progression and later pulmonary impairment. Only a few scientific papers have dealt with the effect of impaired pulmonary function on the physical capacity of these adolescents and adults. Most of these studies show small case numbers, inconclusive stress tests, and divergent results. The aim of this prospective study is to investigate the cardiopulmonary performance capacity and the pulmonary microbiome of adolescent and adult patients with corrected esophageal atresia and to compare the results with a control group. Another focus of the investigators is on the composition of the pulmonary microbiome of the participants. Changes of the pulmonary microbiome and the influence on the cardio-pulmonary performance capacity have not yet been investigated. Furthermore, it should be investigated whether the treatment measures and a complicated disease course in the neonatal period have long-term effects on lung function, exercise capacity and composition of the microbiome in the lungs.

NCT ID: NCT03753880 Recruiting - Bile Leak Clinical Trials

Hemopatch for Prevention of Bile Leaks After Liver Resection

Start date: October 23, 2019
Phase: N/A
Study type: Interventional

In liver surgery bile leaks are still a major cause of postoperative morbidity with the need for additional diagnostic tests, additional interventions, prolonged hospital stay, mortality and higher costs. Efforts to further reduce the rate of postoperative biliary morbidity are therefore important.A new polyethylene glycol (PEG)-coated collagen pad (Hemopatch®) showed faster and more sustained hemostasis, less blood loss, and lower hematoma formation than the fibrin-coated collagen patch in an animal model. This might be attributed to an improved tissue adherence of the PEG-coated pad. We hypothesize that this strong adherence to the hepatic resection surface may also serve as a mechanical sealant of bile ducts thus preventing biliary leakage. To date, there exists no study including a sufficient number of patients to clarify whether sealing of the hepatic resection surface with Hemopatch® can reduce the rate of biliary leaks and data regarding the expected difference in the incidence of biliary complications are lacking.

NCT ID: NCT03751462 Recruiting - Cataract Clinical Trials

Prediction of Pseudophakodonesis of Intraocular Lenses

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Compare visual acuity of patients after cataract surgery with implantation of an IOL clinical outcome measure in eyes with and without pseudoexfoliation syndrome or history of ocular trauma.

NCT ID: NCT03751254 Recruiting - Cataract Clinical Trials

Comparison of Stellaris Standard Infusion With Stellaris Elite

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Clinical performance of phacoemulsification platform Stellaris Elite with standard irrigation fluid bottles in myopic eyes. Anterior chamber depth and patients comfort will be compared between the two groups.

NCT ID: NCT03751241 Recruiting - Pseudophakia Clinical Trials

Reading Quality in Three Different Patient Groups

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Influence of different ophthalmic conditions after cataract surgery (extended range of vision IOL (EROV) with micromonovision, minimonovision with standard IOL and single focus distance vision with standard IOL) on reading quality.

NCT ID: NCT03751215 Recruiting - Cataract Clinical Trials

Anterior Chamber Depth Variability Between Two Lenses With Different Materials

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Compare the change of the Anterior chamber depth (ACD) variability between the Clareon and the AcrySof Intraocular lens (IOL) after implantation over 6 months.

NCT ID: NCT03750149 Recruiting - Glaucoma Clinical Trials

Reading Analysis in Ophthalmologic Patients

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Investigation of the reading parameters and fixation behavior in patients with different ocular diseases (age-related macular degeneration, glaucoma, diabetic maculopathy, epiretinal membrane) and healthy subjects. In addition, fixation analysis and retinal sensitivity measurements will be done with a microperimeter in each subject.

NCT ID: NCT03749798 Recruiting - Cataract Clinical Trials

Comparing an Intraoperative vs. a Standard Wavefront Device

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Comparison of intraoperative measured wavefront data with pre- and post-operative wavefront data.

NCT ID: NCT03749759 Recruiting - Cataract Clinical Trials

Perioperative Stress and Pain Perception of Second Eye Cataract Surgery

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Purpose of this study is to find a correlation between agitation (stress) indicating parameters and the pain perception during second eye cataract surgery, compared to first eye cataract surgery.

NCT ID: NCT03749486 Recruiting - Cataract Clinical Trials

High Resolution Immersion Ultrasound for iIOL Power Calculation

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Assess is the additional use of high resolution immersion ultrasound measurements improve the refractive outcome after cataract surgery.