Status | Study |
RECRUITING |
Study Name: ACS Monitoring Charit� Berlin Condition: Compartment Syndromes Date: 2023-09-01 Interventions: Patients will be monitored about every hour (+/- 30 min) for a total of 8 hours.Measurement time might be extended in case the patient unde |
RECRUITING |
Study Name: NIRST and ICG-based Perfusion Imaging in Acute Compartment Syndrome Condition: Compartment Syndromes Date: 2023-01-03 Interventions: Lower extremity and/or upper extremity surgery |
Recruiting |
Study Name: Near Infrared Spectroscopy in Patients Undergoing Robotic Assisted Laparoscopic Surgery in the Trendelenburg Position Condition: Nontraumatic Compartment Syndrome of Leg Date: 2016-07-07 Interventions: Device: NIRS Monitoring (SenSmart Monitor) |
Not yet recruiting |
Study Name: Abdominal Compartment Syndrome : Diagnostic and Prognostic Value of CT Findings - a Prospective Study Condition: Intra-Abdominal Hypertension Abdominal Compartment Syndrome Date: 2016-06-16 |
Not yet recruiting |
Study Name: Abdominal Compartment Syndrome and Ruptured Aortic Aneurysm : Validation of a Predictive Test Condition: Abdominal Compartment Syndrome Date: 2016-05-09 Interventions: Procedure: ruptured aortic aneurysm All patients with ruptured abdominal aortic aneurysm may be included |
Enrolling by invitation |
Study Name: an Educational Program About Abdominal Compartment Syndrome Condition: Intraabdominal Hypertension Date: 2015-12-17 Interventions: Procedure: transducer technique the nurses will receive the intervention ( the transducer method) to mea |
Completed |
Study Name: This Study Performed to Develop a New Technique for Measuring the Intra Abdominal Pressure Condition: Abdominal Compartment Syndrome Date: 2014-12-07 Interventions: Other: Intraocular pressure measurement with 9 mmHg insufflation |
Completed |
Study Name: The Effect of Different Types of Temporary Abdominal Closure on Intra Abdominal Hypertension. Condition: Intra Abdominal Hypertension Abdominal Compartment Syndrome Date: 2014-08-28 |
Completed |
Study Name: Double Blinded, Randomized Clinical Trial of the Twin Star ECSPRESS Monitoring System for the Reduction of the Incidence of Fasciotomy Condition: Compartment Syndrome Date: 2013-06-11 Interventions: Device: ECSPRESS catheter with active vacuum |
Completed |
Study Name: Phase I, Arteriocyte Magellan MAR01 Therapy - Compartment Syndrome and Battlefield Trauma Condition: Compartment Syndrome Date: 2013-04-17 Interventions: Device: Magellan® Other Names: autologous cell concentrate |