Surgical Emergency Flows and Delays in Admission to the Operating Room
NCT ID: NCT04585529
Last Updated: 2021-05-26
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
1149 participants
OBSERVATIONAL
2020-10-05
2021-03-15
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.
Medical Management Survey : Organization of Perioperative Practices in Anesthesia and Ambulatory Surgery
NCT02380430
Impact of Implementing a National Classification of Surgical Emergencies on Postoperative Morbidity and Mortality: a Prospective Multicenter Observational Study After Implementation.
NCT07317635
Interruptions, Teamwork, Stress and Patient Outcomes in the Operating Room
NCT04226391
Improvement of Intraoperative Behavior of Staff to Prevent Postoperative Complications
NCT03158181
Outcomes of Urological Surgery During Periods of Social COVID-19 Containemnt: is it Reasonable to Limit Access to Surgical Care for All?
NCT04352699
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.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* at least 18 ys old
* decision for unplanned surgery (which should be performed within 72 hours according to the protocol)
* in one of the following hospitals: Lille University hospital, Grenoble University hospital, Strasbourg University hospital, Paris University hospitals (Européen Georges Pompidou, Beaujon, H. Mondor), Lyon University hospital (Hôpital E. Herriot, Lyon Sud), Angers University hospital, Anthony Private hospital).
Exclusion Criteria
* interventional radiology
* endoscopies
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Société Française d'Anesthésie et de Réanimation
OTHER
University Hospital, Lille
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.
Delphine GARRIGUE, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Lille, France
Benoit TAVERNIER, MD, PhD
Role: STUDY_CHAIR
University Hospital, Lille, France
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University hospital
Angers, , France
Clinique
Antony, , France
Beaujon Hospital
Clichy, , France
Henri Mondor Hospital
Créteil, , France
University Hospital
Grenoble, , France
University hospital
Lille, , France
Edouard Herriot Hospital
Lyon, , France
Hôpital sud
Lyon, , France
HEGP
Paris, , France
University Hospital
Strasbourg, , 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.
NI2020/01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.