Abgeschlossene Studien
Adverse Drug Reactions in Emergency Departments
Die ADRED-Studie ist eine multizentrische, prospektive Beobachtungsstudie. In dieser Studie werden unerwünschte Arzneimittelwirkungen (UAW) untersucht, die zu Krankenhausnotfallbehandlungen geführt haben
BONN Cerebral Oxygen Risk Evaluation
Präoperative Risikoevaluation: Stellenwert der zerebralen Oxygenierung bei nicht kardiochirurgischen Patienten mit schwerer Allgemeinerkrankung
Outcomes and Safety Trial Investigating Ecallantide's Effect on Reducing Surgical Blood Loss Volume in Subjects at High Risk of Bleeding Exposed to Cardio-pulmonary Bypass During Cardiac Surgery
Clinicaltrials.gov: NCT00888940
EudraCT: 2008-008354-23
Observational study to determine the optimal timing for surgery following SARS-CoV-2 infection and assess key global surgery indicators
Clinicaltrials.gov: NCT04509986
Prospektive multizentrische Beobachtungsstudie des Effekts des perioperativen Managements von RAAS Modulatoren vor elektiven operativen Eingriffen
EMMAperiop untersuchte die Effekte eines präoperativen Pausierens oder Fortführens einer Renin-Angiotensin-Aldosteron-System-Inhibitor-Therapie (RAAS-I) im Hinblick auf perioperative kardiovaskuläre Ereignisse
European registry for Studying the Treatment of Acute Hypertension
Characteristics, practice patterns, and outcomes in patients with acute hypertension
European Surgical Outcomes Study - multi-centre, international cohort study of peri-operative care and clinical outcomes for patients undergoing non-cardiac surgery
Clinicaltrials.gov: NCT01203605
A research study which aims to help improve the care of patients who undergo surgery in the future
Impact of PReOperative Midazolam on OuTcome of Elderly patients (I-PROMOTE)
The study aimed to assess, if placebo compared to preoperative administration of midazolam in elderly patients is equal in regard to the global postoperative patient satisfaction
Clinicaltrials.gov: NCT03052660
EudraCT Nummer: 2016-004555-79
Safety and Efficacy of 6% Hydroxyethyl Starch (HES) Solution Versus an Electrolyte Solution in Patients Undergoing Elective Abdominal Surgery
Clinicaltrials.gov: NCT03278548
EudraCT: 2016-002162-30
Pragmatic, prospective, randomized, controlled, double-blind, multi-centre, multinational study on the safety and efficacy of a 6% Hydroxyethyl starch (HES) solution versus an electrolyte solution in trauma patients
Clinicaltrials.gov: NCT03338218
EudraCT: 2016-002176-27
Continuous Respiratory Monitoring on the General Ward
Clinicaltrials.gov: NCT03571646
Management of Myokardial Injury After Noncardiac Surgery Trial
Diese multizentrische, internationale und randomisiert-kontrollierte Studie untersuchte die Wirkung des Blutverdünners Dabigatran in Patienten die postoperativ einen Herzinfarkt erlitten haben
Clinicaltrials.gov: NCT01082874
Phase II Study to Compare MDCO-2010 vs Placebo and Tranexamic Acid in Patients Undergoing Cardiac Surgery
Clinicaltrials.gov: NCT01530399
EudraCT: 2011-004666-15
Pediatric AirWay complicationS COVID-19
A Double-Blind Multicenter Study of the Safety and Efficacy of Parecoxib Sodium/Valdecoxib and Placebo/Valdecoxib Compared to Placebo for Treatment of Post-Surgical Pain in Patients Who Have Coronary Bypass Graft Via Median Sternotomy
Clinicaltrials.gov: NCT00636064
Safety and effectiveness of a Patient Blood Management (PBM) program in surgical patients
Clinicaltrials.gov: NCT01820949
Prospective Evaluation of a RIsk Score for Postoperative Pulmonary COmPlications in Europe
Clinicaltrials.gov: NCT01346709
Prediction of Opioid-Induced Respiratory Depression on Inpatient Wards Using Continuous Capnography and Oximetry
Clinicaltrials.gov: NCT02811302
PROtective Ventilation using HIgh versus LOw levels of positive end-expiratory pressure (PEEP) during general Anesthesia for open abdominal surgery
Clinicaltrials.gov: NCT01441791
Protective intraoperative ventilation with higher versus lower levels of positive end-expiratory pressure in obese patients
Prä-Operative Prädiktion eines postoperativen Delirs durch geeignetes Screening
Das Ziel dieser monozentrischen, nicht-interventionellen Beobachtungstudie ist die Entwicklung eines Instrumentes zur Vorhersage des Risikos für postoperatives Delir aus präoperativen Routinedaten.
DRKS-ID der Studie: DRKS000157154
PeriOperative ISchemic Evaluation-2 Trial
Multizentrische, internationale und randomisiert-kontrollierte Studie die untersucht hat, ob eine perioperative Einnahme von Acetylsalicylsäure und/oder Clonidin die 30 Tage Mortalität bzw. die Inzidenz postoperativer Myokardinfarkte beeinflussen kann
Clinicaltrials.gov: https://www.clinicaltrials.gov/ct2/show/NCT01082874
Phase IIIb Study of APD421 in Combination as PONV Prophylaxis
Clinicaltrials.gov: NCT02337062
Retrospektive monozentrische Studie zur Validierung des POSTPOM scores zur Prädiktion postoperativer Sterblichkeit
Large, european, multi-centre, prospective observational cohort study. Aim of the study was to determine the peri-interventional (surgical and non-surgical interventional) all-cause mortality rate in geriatric patients
POSE wird alle älteren Patienten (≥80 Jahre), unabhängig davon welchem interventionellen Eingriff sie sich mit Anästhesiebeteiligung unterziehen, untersuchen.
Clinicaltrials.gov: NCT03152734
POstaneasthesia PULmonary complications After use of muscle Relaxants in europe
Clinicaltrials.gov: NCT01865513
The Effect Of Acadesine On Reducing Cardiovascular and Cerebrovascular Adverse Events In Coronary Artery Bypass Graft (CABG) Surgery
Clinicaltrials.gov: NCT00872001
EudraCT: 2008-002518-23
Remote Ischemic Preconditioning for Heart Surgery
Der Zweck dieser Studie war es, die Auswirkungen der Remote Ischemic Preconditioning (RIP) auf perioperative ischämische Verletzung bei Patienten, die sich einer Herzoperation unterziehen zu bewerten
Clinicaltrials.gov: https://clinicaltrials.gov/ct2/show/NCT01067703
Rückentherapie mit multimodaler Schmerztherapie
Das Projekt untersucht, ob eine multimodale, interdisziplinäre und die Versorgungsbereiche übergreifende Therapie gemäß des IV-Vertrages (Integrierte Versorgung) einer Behandlung der Regelversorgung überlegen ist.
A randomized, safety-assessor blinded trial comparing 4.0 mg.kg-1 sugammadex with placebo in adult subjects scheduled for surgery requiring profound neuromuscular blockade
Der Zweck dieser internationalen, randomisiert-kontrollierten Interventionsstudie war es, die Sicherheit und Wirksamkeit von Sugammadex zu bewerten, wenn verabreicht nach dem tatsächlichen Körpergewicht (ABW) im Vergleich zum idealen Körpergewicht (IBW)
Clinicaltrials.gov: https://clinicaltrials.gov/ct2/show/NCT03346070
Registrierslink zur Studie: https://ichgcp.net/de/clinical-trials-registry/NCT03346070
A randomized, safety-assessor blinded trial comparing 4.0 mg.kg-1 sugammadex with placebo in adult subjects scheduled for surgery requiring profound neuromuscular blockade
Clinicaltrials.gov: NCT00758485
EudraCT: 2008-002518-23
The aim of the investigators' research program is to investigate the effects of perioperative high dose selenium supplementation in high-risk cardiac surgical patients undergoing complicated open heart surgery
Clinicaltrials.gov: NCT02002247
Occurrence of Bleeding and Thrombosis during Antiplatelet therapy in Non-cardiac surgery
Clinicaltrials.gov: NCT01358422
A Study to Explore the Influence of Two Opioid Pain Medications on Bacterial Composition in the Gut and Other Gastrointestinal Aspects
Clinicaltrials.gov: NCT01915147
EudraCT: 2012-001772-11
Phase 3 for Prevention of Major Adverse Kidney Events (MAKE) in Subjects at High Risk for AKI Following Cardiac Surgery
Clinicaltrials.gov: NCT03510897
EudraCT: 2018-000757-49
