Systolic Pressure Index in Assessing the Risk of Cardiovascular Events
NCT ID: NCT00925964
Last Updated: 2012-03-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
504 participants
OBSERVATIONAL
2008-01-31
2009-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Post-operative Cardiac Outcome of Non-cardiac Surgery Predicted by INVOS
NCT02079454
Evaluation of the Brain Natriuretic Peptide as a Predictor of Morbidity and Mortality in Cardiac Surgery
NCT00699673
Non-invasive Blood Pressure Monitoring in Carotid Surgery
NCT06965257
Perioperative Individualized Optimization of Mean Arterial Pressure in Cardiac Surgery
NCT05403697
Ventricular-Arterial Coupling: A Predictor of Post-Induction Hypotension
NCT05969886
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients exposed
Patients with Systolic Pressure Index \<0,9 ou \>1,4.
No interventions assigned to this group
Patients not exposed
Patients with Systolic Pressure Index \>0,9 ou \<1,4.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* surgery set :
* Visceral surgery: gastrectomy or colectomy, abdomino-perineal amputation, pancreatic surgery, liver surgery, esophageal surgery
* In urological surgery: nephrectomy, total prostatectomy, cystectomy
* In thoracic surgery: pneumonectomy, lobectomy
* In orthopedic surgery: total hip replacement and total knee prosthesis
Exclusion Criteria
* life expectancy less than 6 months
* emergency surgery
40 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Limoges
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Philippe LACROIX, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Limoges
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Explorations fonctionnelles vasculaires et angiologie (Hôpital Dupuytren)
Limoges, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
I07029
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.