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NCT ID: NCT02207894 Recruiting - Haemophilia A Clinical Trials

A Survey on the Success of Inhibitor Elimination Using Individualized Concentrate Selection and Controlled ITI

Start date: August 2006
Phase:
Study type: Observational

This research program is initiated to evaluate and document data on the success of ITI in 300 haemophilia A patients with newly developed or already existing FVIII-inhibitors (also patients who might potentially have failed in earlier ITIs), which will be treated with ITI - preferably high-dose based on individualized product selection, in order to improve management of this potentially devastating complication of haemophilia treatment. In order to investigate the role of in vitro tests on individual ITI success rate in patients undergoing ITI, the inhibitor plasma samples can be assayed against different FVIII concentrates using the following in vitro tests: Batch selection, Thrombin generation assay (TGA), Thrombin Generation Test (TGT) to monitor FVIII efficacy, Epitope mapping,IgG Subclasses specific for FVIII, Immunogenotyping.

NCT ID: NCT02200874 Recruiting - Malnutrition Clinical Trials

Investigation of the Effectiveness and Efficiency of a Structural Clinical Nutrition Support

Start date: November 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the effectiveness and efficiency of a structural clinical nutrition support by an interdisciplinary Nutrition Support Team. To do this we examine nutritional management and its economic impact as well as the nutritional status of patients of University Hospital Tübingen before and after the implementation of a Nutritional Support Team.

NCT ID: NCT02196597 Recruiting - Quality of Life Clinical Trials

Value of Anorectal Manometry Before Ileo- or Sigmoidostomy Closure After Rectal Resection

Start date: January 2013
Phase: N/A
Study type: Observational

Background: High prevalence of fecal incontinence after rectal resection in patients with rectal carcinoma. Hypothesis: Anorectal manometry done before ileostomy or sigmoidostomy closure can predict fecal incontinence. Methods: Anorectal manometry before, 1 month and 6 month after closure. Anorectal endosonography before and 1 month after closure. Prediction of postoperative incontinence by the surgeon (digital sphincter examination). Visual analog scales for continence, subjective success of operation, and global well being; Wexner and Vaizey incontinence score; Parks incontinence classification; Rockwood fecal incontinence quality of life score; each before, 1 and 6 month after closure.

NCT ID: NCT02192619 Recruiting - Relapsed APL Clinical Trials

National Acute Promyelocytic Leukemia (APL) Observational Study NAPOLEON-Registry of the German AML Intergroup

Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

The registry aims to document epidemiologic data, treatment and long-term outcome as well as quality of life of patients with APL. Additionally, a biobanking project for further translational studies is integrated. Prospective population-based non-interventional and non-randomized multicenter registry.

NCT ID: NCT02190383 Recruiting - Tic-Disorder Clinical Trials

Efficacy of a Habit Reversal Treatment on Tic-symptoms

Start date: November 2013
Phase: N/A
Study type: Interventional

The main purpose of this study is to evaluate the efficacy of a habit reversal based treatment programme in children and adolescents aged 8 to 18 years with tic disorders.

NCT ID: NCT02190370 Recruiting - Tic-Disorder Clinical Trials

Efficacy of a Resources Activation Treatment on Tic-symptoms

Start date: November 2013
Phase: N/A
Study type: Interventional

The main purpose of this study is to evaluate the efficacy of a resources activation based treatment programme in children and adolescents aged 8 to 18 years with tic disorders.

NCT ID: NCT02187432 Recruiting - Clinical trials for Autosomal Dominant Polycystic Kidney Disease

The Eurocyst Initiative: Building a Network of ADPKD Reference Centers Across Europe

Start date: August 2013
Phase: N/A
Study type: Observational

EuroCYST initiative aims to build a large, well-characterized cohort of Autosomal Dominant polyCYSTic Kidney Disease (ADPKD) subjects who are followed in a longitudinal observational cohort study has the potential to identify progression factors and biomarkers, and to assess disease stage specific mortality, morbidity and health care costs.

NCT ID: NCT02187263 Recruiting - Amyloidosis Clinical Trials

German Centre for Cardiovascular Research Cardiomyopathy Register

TORCH
Start date: December 2014
Phase: N/A
Study type: Observational [Patient Registry]

This is a joint project by Heidelberg University and Greifswald University. Our objective is to establish an unique national multi-center registry and biobank of well phenotyped patients with non-ischemic cardiomyopathies (CMP) including in depth clinical, molecular and omics-based phenotyping to serve as: 1. central hub for clinical outcome studies. 2. joint resource for diagnostic and therapeutic trials. 3. common biomaterial bank. 4. resource for detailed molecular analyses on patients' biomaterials and patient specific model systems.

NCT ID: NCT02186886 Recruiting - Ulcerative Colitis Clinical Trials

Physiological Intermolecular Modification Spectroscopy (PIMS) in Ulcerative Colitis With Golimumab

Start date: June 2014
Phase: Phase 4
Study type: Interventional

Aim of this study is to determine wether the macromolecular spectral characteristic of ulcerative colitis patients - measured by Physiological Intermolecular Modification Spectroscopy (PIMS) - is a predictive factor for response to Simponi treatment

NCT ID: NCT02181855 Recruiting - Clinical trials for Objectified Gastroesophageal Reflux Disease

Effect of Full-thickness Gastroplication With the GERD-X System on Atypical Gastro-esophageal-reflux-symptoms

Start date: June 2014
Phase: N/A
Study type: Interventional

Patients with atypical symptoms of objectified gastroesophageal reflux disease will be treated by full-thickness gastroplication and the effect of this intervention will be measured by questionnaires and clinical diagnostics (for example pH/MII).