Interventionell Ultrasound
Conditions
Interventions
Group 1: prospective observational study of ultrasound-guided abdominal interventions in adults
Sponsors
Medizinische Hochschule Brandenburg Theodor FontaneBrandenburgisches Institut Klinischer Ultraschall (BIKUS)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The study will include diagnostic and/or therapeutic interventions under continuous ultrasound imaging percutaneously or transcavitary (endosonographic) in the abdomen and/or retroperitoneum in patients aged eighteen years and older. Including simple punctures for fluid or tissue removal up to more complex drainage therapies as well as ablation and sclerotherapy procedures.
Exclusion criteria
Exclusion criteria: Diagnostic or therapeutic ascites punctures, procedures in the prostate region and outside the abdomen, e.g. on the thorax (including the mediastinum) or on the extremities and joints, should not be included. Lack of patient consent to participate in the study. Children and adolescents not completed 18 years of age.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study objective is to test a web-based documentation system for the collection of routine data related to ultrasound-assisted procedures and to evaluate the selected collection parameters for analyzability with respect to the following endpoints: 1. frequency of immediate complications (e.g., bleeding) and late complications (especially infections), overall morbidity and mortality. 2. predictors of inadequate intervention outcomes and of complications 3. effectiveness of measures for complication prevention 4. frequency, range of methods and effectiveness of the use of INVUS for the treatment of abscesses. | — |
Countries
Germany
Contacts
Public ContactNicole Eder
Krankenhaus Märkisch-Oderland GmbH
Outcome results
None listed