Stroke Volume Versus Inferior Vena Cava Collapsibility Index to Predict Postinduction Hypotension in Intestinal Obstruction
1 other identifier
observational
75
0 countries
N/A
Brief Summary
Postinduction hypotension (PIH) is a frequent complication during general anesthesia. This study aims to compare the predictive effectiveness and diagnostic accuracy of stroke volume (SV) measured via left ventricular outflow tract velocity time integral (LVOT-VTI) versus the inferior vena cava collapsibility index (IVC-CI) using transthoracic echocardiography. The assessment will be conducted in adult patients with intestinal obstruction undergoing exploratory abdominal surgery under general anesthesia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2026
Shorter than P25 for all trials
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
First Submitted
Initial submission to the registry
July 29, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
CompletedFirst Posted
Study publicly available on registry
August 3, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 1, 2027
August 3, 2026
July 1, 2026
6 months
July 29, 2026
July 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Efficacy of SV versus IVC-CI as Predictors for Post-Induction Hypotension Efficacy of SV versus IVC-CI as Predictors for Post-Induction Hypotension
Comparison of the effectiveness and diagnostic accuracy (AUC) of stroke volume (SV) measured via LVOT-VTI versus inferior vena cava collapsibility index (IVC-CI) measured via TTE in predicting post-induction hypotension. Comparison of the effectiveness and diagnostic accuracy (AUC) of stroke volume (SV) measured via LVOT-VTI versus inferior vena cava collapsibility index (IVC-CI) measured via TTE in predicting post-induction hypotension.
Measured baseline pre-induction and compared immediately post-induction.
Secondary Outcomes (3)
Incidence of Post-Induction Hypotension Incidence of Post-Induction Hypotension
Within 3 minutes following induction of general anesthesia.
Length of Hospital Stay Length of Hospital Stay
From date of surgery until hospital discharge (up to 9 months).
Time to Recovery from Post-Anesthesia Care Unit (PACU) Time to Recovery from Post-Anesthesia Care Unit (PACU)
Intraoperative / immediate postoperative period until PACU discharge (up to 24 hours).
Eligibility Criteria
Adult patients diagnosed with intestinal obstruction scheduled for exploratory abdominal surgery under general anesthesia at Ain-Shams University Hospitals.
You may qualify if:
- Adult patients with intestinal bowel obstruction undergoing exploratory abdominal surgery under general anesthesia.
- Age 40 to 70 years old.
- Body Mass Index (BMI) = 18 to 25 kg/m2.
- American Society of Anesthesiologists (ASA) physical status grade I or II.
You may not qualify if:
- American Society of Anesthesiologists (ASA) physical status grade \>= III.
- Patients in whom the IVC cannot be visualized or patients with poor echogenicity.
- Patients with hemodynamic instability.
- Patients with vascular, respiratory, or cardiac diseases (e.g., cardiomyopathy, heart valve disease, arrhythmia, or bad exercise tolerance).
- Pregnant patients.
- Difficult airway or multiple intubatio
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Mohamed H Shokeir, M.D., Ph.D.
Ain Shams University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 29, 2026
First Posted
August 3, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
February 1, 2027
Last Updated
August 3, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared to protect patient privacy and confidentiality.