Clinical trials: Compartment Syndrome
Abdominal Compartment Syndrome
This Study Performed to Develop a New Technique for Measuring the Intra Abdominal Pressure
The purpose of this study is to evaluate the changes of intraocular pressure due to the increase of intra abdominal pressure.
- Trial name
- NCT02319213
- Testing
- Intraocular pressure measurement with 9 mmHg insufflation, Intraocular pressure measurement with 12 mmHg insufflation, Intraocular pressure measurement with 15 mmHg insufflation
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Selcuk University
Human Volunteers
In Vivo Optical Spectroscopy Monitoring in a New Model of Muscular Compartment Syndrome
Muscular compartment syndrome (MCS) is consecutive to an increase in intramuscular compartment pressures, and is a rare but serious postoperative complication.
- Trial name
- NCT01452425
- Testing
- Tourniquet, INVOS assessment, EMG assessment
- Where
- Belgium
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Université Catholique de Louvain
Traumatic Brain Injuries, Intracranial Hypertension
Security and Effectiveness Assessment of Locking Systems in Ventriculostomy for Traumatic Brain Injury
This study aims to compare the effectiveness and safety of a standard intervention called ventriculostomy for managing increased intracranial pressure (ICP) in patients with severe traumatic brain injury (TBI).
- Trial name
- SEALS-TBI (NCT06772155)
- Testing
- Ventriculostomy, Ventriculostomy + Locking Device
- Volunteers
- 292 people
- Sponsor
- Meditech Foundation
Open Abdomen, Fascial Closure
Vacuum Assisted Wound Closure (VAWC) and Mesh Mediated Fascial Traction
The purpose of this multicenter trial is to prospectively evaluate a novel combination of vacuum assisted wound closure (VAWC) and mesh mediated fascial traction for closure of open abdomens.
- Trial name
- NCT00494793
- Testing
- VAWC and mesh mediated fascial traction
- Where
- 5 sites in Sweden
- Volunteers
- 111 people
- Sponsor
- Skane University Hospital
Compartment Syndromes, Compartment Syndrome of Lower Leg
NIRST and ICG-based Perfusion Imaging in Acute Compartment Syndrome
This is a prospective observational study of patients with suspected Acute Compartment Syndrome. The primary objective of this work is to determine whether intensity changes associated with the NIRST signal, reflecting oxy- and…
- Conditions
- Compartment Syndromes, Compartment Syndrome of Lower Leg, Compartment Syndrome of Forearm
- Trial name
- NCT05672381
- Testing
- Lower extremity and/or upper extremity surgery
- Where
- United States
- Volunteers
- 15 people
- Sponsor
- Dartmouth-Hitchcock Medical Center
Intra-abdominal Hypertension
Efficacy and Safety Profile of Cisatracurium Besylate for IAH
This study is a randomized, double-blinded, controlled design. In this study, Cisatracurium Besylate was selected for treatment in Intra-abdominal hypertension or abdominal compartment syndrome,accompanied with evaluating the…
- Trial name
- NCT05172531
- Testing
- Cisatracurium Besylate, saline 0.12ml/kg/hr
- Volunteers
- 80 people
- Sponsor
- Tianjin Nankai Hospital
Ischemia Limb, Blood Circulation Disorder
Ischemia Detection During Development of Acute Compartment Syndrome
This is an open, observational, prospective, descriptive, single-centre study including 60 patients. The study is designed to investigate if IscAlert sensor system can be used for reliable and continuous tissue carbon dioxide…
- Conditions
- Ischemia Limb, Blood Circulation Disorder, Carbon Dioxide, Biosensing Techniques
- Trial name
- IDEA (NCT06079255)
- Testing
- IscAlert sensor(s) in patient with risk of acute compartment syndrome
- Where
- Norway
- Volunteers
- 60 people
- Sponsor
- Oslo University Hospital
Acute Limb Ischemia
Evaluation of Acute Lower Limb Ischemia
The primary objective of this study is to evaluate the effect of different treatment modalities on clinical outcome of patients suffering from acute lower limb ischemia (ALI).
- Trial name
- PROMOTE-ALI (NCT05138679)
- Testing
- Revascularization, Primary major amputation, Best medical treatment
- Where
- 37 sites in Austria, Croatia and 8 more
- Volunteers
- 700 people
- Sponsor
- Medical University Innsbruck
Compartment Syndrome Traumatic Lower Extremity
BM-MNCs for Lower Extremity Compartment Syndrome Injury
This is a phase 1 study to assess safety and tolerability of intramuscular administration of two different doses of autologous bone marrow mononuclear cells (BM-MNCs) for treatment of lower extremity injury complicated by…
- Trial name
- NCT03880656
- Testing
- Intramuscular administration of autologous BM-MNCs
- Where
- United States
- Volunteers
- 18 people
- Sponsor
- Oregon Health and Science University
Compartment Syndrome
Double Blinded, Randomized Clinical Trial of the Twin Star ECSPRESS Monitoring System for the Reduction of the Incidence of Fasciotomy
The proposed study is a double-blinded, randomized clinical trial of tissue pressure monitoring only (Control group) vs. tissue pressure monitoring plus tissue ultrafiltration (Treatment group) in patients with tibia fractures…
- Trial name
- ECSPRESS (NCT01879696)
- Testing
- ECSPRESS catheter with active vacuum
- Where
- United States
- Volunteers
- 150 people
- Sponsor
- Twin Star Medical, Inc.
Intra-Abdominal Hypertension, Postoperative Complications
The Impact of Intra-Abdominal Pressure on Mortality and Morbidity in Patients Undergoing Open-Heart Surgery
This prospective observational study evaluated whether increased intra-abdominal pressure, meaning increased pressure inside the abdomen, is associated with postoperative complications and mortality in adults undergoing elective…
- Trial name
- NCT07752082
- Where
- Turkey (Türkiye)
- Volunteers
- 100 people
- Sponsor
- Bursa Yuksek Ihtisas Training and Research Hospital
Intraabdominal Hypertension
an Educational Program About Abdominal Compartment Syndrome
Early detection of intra-abdominal hypertension is essential to the prevention of abdominal compartment syndrome and requires close surveillance of intra-abdominal hypertension in patients at increased risk.
- Trial name
- Ghada (NCT02639013)
- Testing
- transducer technique
- Where
- Egypt
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Assiut University
Intra-Abdominal Hypertension
Intra-abdominal Hypertension and Associated Factors Among Patients Admitted in Intensive Care Units in Uganda.
The study was carried out to determine the prevalence,incidence and factors associated with intra-abdominal hypertension among patients admitted in three intensive care units in Kampala Uganda.
- Trial name
- NCT03567265
- Where
- Uganda
- Volunteers
- 126 people
- Sponsor
- Makerere University
Intra-Abdominal Hypertension
Intra-abdominal Pressure (IAP) During PFA Treatment of A-fib/ A-Flutter
The purpose of this study is to investigate the intra-abdominal pressure utilizing the Accuryn monitoring system during pulsed field ablation procedures in the electrophysiology lab compared to the type of anesthetic utilized.
- Trial name
- IAP (NCT06876896)
- Testing
- Accuryn Foley catheter device
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- Wake Forest University Health Sciences
Intraabdominal Hypertension, Multi-Organ Disorder
Correlation Between Intra-abdominal Pressure, Biomarkers of Bacterial Translocation and Intestinal Wall Damage
Main scientific hypotheses of the project: 1. The level of intestinal microflora translocation markers and biomarkers of intestinal wall damage the in the blood serum correlates with the level of intra-abdominal pressure…
- Conditions
- Intraabdominal Hypertension, Multi-Organ Disorder, Translocation Syndrome
- Trial name
- NCT06221293
- Testing
- immunoenzyme analysis
- Where
- 5 sites in Kazakhstan
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Karaganda Medical University
Acute Pancreatitis, Intra-Abdominal Hypertension
Predictive Ability of Intra-Abdominal Pressure for Mortality in Patients With Severe Acute Pancreatitis
Severe Acute Pancreatitis (SAP) is an acute inflammatory condition of the pancreas characterized by organ dysfunction and increased mortality.
- Trial name
- NCT04525027
- Testing
- intra-abdominal pressure in severe acute pancreatitis
- Where
- India
- Volunteers
- 360 people
- Sponsor
- Post Graduate Institute of Medical Education and Research, Chandigarh
Chronic Exertional Compartment Syndrome
Utilization of High Frequency Ultrasound to Diagnose Chronic Exertional Compartment Syndrome
The purpose of this study is to investigate high frequency ultrasound as a future modality for the diagnosis of chronic exertional compartment syndrome (CECS).
- Trial name
- NCT03736174
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- University of Colorado, Denver
Acute Respiratory Distress Syndrome, Acute Kidney Injury
Prone Position and Renal Resistive Index
Patients suffering from Acute Respiratory Distress Syndrome (ARDS) with a prone position (PP) indication will benefit from measurements of renal resistive index, intra-abdominal pressure (IAP), urinary oxygen tension (uPO2) and…
- Conditions
- Acute Respiratory Distress Syndrome, Acute Kidney Injury, Prone Position, Intra-Abdominal Hypertension
- Trial name
- PRO-KIDNEY (NCT04286490)
- Testing
- Prone position
- Where
- France
- Volunteers
- 20 people
- Sponsor
- University Hospital, Grenoble
Osteonecrosis, Pseudarthrosis
Musculoskeletal Non-tumoral Pathology Quantitative Perfusion
Study on quantitative perfusion parameters acquired on MR imaging of patients with non-tumoral pathology of the musculoskeletal system.
- Conditions
- Osteonecrosis, Pseudarthrosis, Compartment Syndrome
- Trial name
- AFRONT (NCT02683252)
- Testing
- T1 mapping and MR perfusion acquisition
- Where
- 2 sites in France
- Volunteers
- 400 people
- Sponsor
- Central Hospital, Nancy, France
Critical Illness, Acute Kidney Injury
Collective Accuryn Physiologic Signals and Signatures
The CAPSS Study is a retrospective and prospective, multi-center, single-arm post-market data collection study with an FDA cleared device.
- Conditions
- Critical Illness, Acute Kidney Injury, Sepsis, Septic Shock
- Trial name
- CAPSS (NCT03817281)
- Testing
- Accuryn Monitoring System
- Where
- United States
- Sponsor
- Potrero Medical