Echocardiography-derived Pre-induction Hemodynamic Phenotypes and Post-induction Hypotension: an Exploratory Clustering Analysis
1 other identifier
observational
64
1 country
1
Brief Summary
This study evaluated the occurrence of post-induction hypotension (PIH) in patients undergoing elective surgery under general anesthesia. PIH is a common perioperative complication associated with adverse outcomes. Using previously collected clinical and echocardiographic data, the study explored the relationship between pre-induction hemodynamic status and the risk of developing PIH. The findings may help improve preoperative risk stratification and support more individualized perioperative hemodynamic management.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2020
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2020
CompletedFirst Submitted
Initial submission to the registry
March 28, 2026
CompletedFirst Posted
Study publicly available on registry
April 3, 2026
CompletedApril 8, 2026
April 1, 2026
2 months
March 28, 2026
April 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pre-induction hemodynamic phenotype classification
Pre-induction hemodynamic phenotypes were derived using unsupervised clustering of clinical and echocardiographic variables obtained prior to anesthesia induction.
pre-induction, before administration of general anesthesia: from admission to the operating to induction of general anesthesia
Pre-induction hemodynamic phenotype classification
Pre-induction hemodynamic phenotypes were derived using unsupervised clustering of clinical and echocardiographic variables obtained prior to anesthesia induction.
Baseline (pre-induction, before administration of general anesthesia)
Study Arms (1)
Overall Study Cohort
Adult patients undergoing elective surgery under general anesthesia included in a retrospective analysis of prospectively collected data.
Eligibility Criteria
Patients aged over 50 years scheduled for elective abdominal surgery under general anesthesia.
You may qualify if:
- Patients scheduled for elective abdominal surgery under genral anesthesia.
You may not qualify if:
- patients with dyspnoea
- unstable angina,
- severe valvular heart disease
- anticipated or unanticipated difficult airway management
- suspected increased intra-abdominal pressure
- poor echogenicity.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cadi Ayyad University . Avicenna Military Hospital
Marrakesh, Marrakech, 10000, Morocco
Related Publications (1)
Aissaoui Y, Jozwiak M, Bahi M, Belhadj A, Alaoui H, Qamous Y, Serghini I, Seddiki R. Prediction of post-induction hypotension by point-of-care echocardiography: A prospective observational study. Anaesth Crit Care Pain Med. 2022 Aug;41(4):101090. doi: 10.1016/j.accpm.2022.101090. Epub 2022 May 1.
PMID: 35508291RESULT
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of critical care and anesthesiology
Study Record Dates
First Submitted
March 28, 2026
First Posted
April 3, 2026
Study Start
February 1, 2020
Primary Completion
March 30, 2020
Study Completion
March 30, 2020
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR
- Time Frame
- April 30th, 2026
- Access Criteria
- Qualified healthcare providers or researchers De-identified individual participant data (including clinical and echocardiographic variables underlying the reported results)
De-identified individual participant data (including clinical and echocardiographic variables underlying the reported results) will be made available upon reasonable request from qualified healthcare providers or researchers. Data sharing will be subject to approval by the study investigators and compliance with institutional and ethical regulations. Requests must include a methodologically sound proposal and will be evaluated to ensure appropriate use of the data.