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NCT ID: NCT03420131 Recruiting - Clinical trials for Coronary Artery Disease

Diagnostic Agreement of iFR and QFR.

DETECTISCHEMIA
Start date: July 18, 2017
Phase: N/A
Study type: Observational

A Prospective, observational, single center diagnostic study to investigate the the diagnostic agreement between QFR and the pressure wire-based iFR in a real world setting.

NCT ID: NCT03419351 Recruiting - Refractive Errors Clinical Trials

Comparison of a Smartphone Based Self Refraction Tool With Conventional Refraction Error Estimation Methods

Start date: November 20, 2017
Phase: N/A
Study type: Interventional

Self evaluating tools based on smartphone devices are public available on the market for each person. The tools are used to estimate the existing refractive error for each eye of a patient. Hereafter, e.g. ordering glasses via internet could be the next step for this persons. The daily routine within an eye hospital shows, that estimation of the refractive error is a difficult and time consuming procedure. The study compares the results of the measured refractive error using a smartphone based tool with the results of conventional measurement methods.

NCT ID: NCT03418467 Recruiting - Atrial Fibrillation Clinical Trials

Risk Factors in Tachycardiomyopathy

EMPATHY
Start date: October 11, 2018
Phase:
Study type: Observational

Decision between rate control and rhythm control can be a challenge in clinical practice. While there is some guiding evidence, we still lack a comprehensive insight into different subgroups of patients that will benefit from a rhythm control treatment. EMPATHY is a prospective clinical study in patients presenting with heart failure and a tachyarrhythmic rhythm disturbance. Biomarkers, routinely obtained results from clinical examinations, and results from endomyocardial biopsies shall be evaluated to identify patients which have better outcome from a rhythm control strategy by ablation therapy or, if contraindicated by pharmacological rhythm control. This study is designed to identifying risk factors and subgroups profiting from rhythm restoration and therefore improve current therapeutic approaches and the rate of recurrence-free survival.

NCT ID: NCT03417115 Recruiting - Breast Cancer Clinical Trials

Breast Cancer Registry Platform

OPAL
Start date: December 22, 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of the project is to set up a national, prospective, longitudinal, multicenter cohort study with associated satellites, a tumor registry platform, to document uniform data on characteristics, molecular diagnostics, treatment and course of disease, to collect patient-reported outcomes and to establish a decentralized biobank for patients with breast cancer in Germany.

NCT ID: NCT03405389 Recruiting - Clinical trials for Mandibular Fractures

Focused Registry to Collect Clinical Data on the MatrixWAVE System

FRMatrixWAVE
Start date: June 20, 2019
Phase:
Study type: Observational [Patient Registry]

The goal of this registry is to evaluate the performance of the MatrixWAVE(TM) MMF system in patients suffering from non-condylar and/or condylar fractures. The evaluation will focus on the clinical performance in terms of : - surgical technique - application time - intra- and postoperative complications - short term patient-reported outcomes

NCT ID: NCT03403868 Recruiting - Clinical trials for Right Ventricular Dysfunction

Right Ventricular Haemodynamic Evaluation and Response to Treatment

Rightheart I
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

Mono-center Study to evaluate different multimodal functional parameter of the right ventricle in PAH-patients

NCT ID: NCT03402971 Recruiting - Pregnancy Related Clinical Trials

The Right Heart During and After Pregnancy - an Echocardiographic Study

EVA
Start date: November 2, 2017
Phase:
Study type: Observational

The main goal is to establish echocardiographic reference values of the right heart for pregnant women, assuming they differ significantly from those of non pregnant women of same age. Therefore the investigators will use existing reference values published by American society of echocardiography and European Association of Echocardiography. As side arms the investigators want to explore, whether illness of either fetus or mother is connected with right heart affection.

NCT ID: NCT03399383 Recruiting - Clinical trials for Adrenal Insufficiency

Adherence in Chronic Adrenal Insufficiency

Start date: September 2016
Phase: N/A
Study type: Interventional

Adherence, concerns and satisfaction with information in German patients with adrenal insufficiency as well as the influence of a standardized education program will be assessed by a compared cross-sectional and longitudinal study.

NCT ID: NCT03398915 Recruiting - Clinical trials for Degenerative Disc Disease

The European Robotic Spinal Instrumentation (EUROSPIN) Study

EUROSPIN
Start date: February 20, 2018
Phase:
Study type: Observational [Patient Registry]

In a multinational prospective study, preoperative, intraoperative, perioperative and follow-up data on patients receiving thoracolumbar pedicle screw placement for degenerative disease or infections or tumors will be collected. The three arms consist of robot-guided (RG), navigated (NV), or freehand (FH) screw insertion.

NCT ID: NCT03396718 Recruiting - Clinical trials for Head-and-neck Squamous Cell Carcinoma

De-escalation of Adjuvant Radio (Chemo) Therapy for HPV-positive Head-neck Squamous Cell Carcinomas

DELPHI
Start date: September 4, 2018
Phase: N/A
Study type: Interventional

In patients with squamous cell carcinoma of the oral cavity, the oropharynx and larynx with local advanced tumors (pathologic stage T3 = pT3) and or lymph node involvement (pN+) postoperative radio - or radiochemotherapy is the standard of care. Postoperative radiochemotherapy is indicated in patients with multiple lymph node metastasis, lymph node metastasis with extracapsular spread and / or residual tumor (R1-Status) after resection. Oropharyngeal cancer caused by HPV (human papillomavirus 16 or 18) is a distinct subgroup with a known sensitivity to radiotherapy (RTx) or radiochemotherapy (RCTx). Additionally a superior outcome after R(C)Tx over HPV negative patients was shown for patients treated with primary or adjuvant RCTx. To date it is unknown if the total dose of the radiotherapy can be safely reduced with the aim to decrease the therapy associated late effects. Patients with a HPV associated carcinoma that take part in the study will be treated with a reduced radiotherapy dose, chemotherapy will be prescribed based on clinical factors (number of affected lymph node, presence of extracapsular spread or residual tumor). Radiation dose will be reduced in two steps.