Actively Recruiting

Age: 65Years +
All Genders
NCT06814054

Carotid Artery Corrected Flow Time and Inferior Vena Cava Collapsibility Index for Prediction of Hypotension After Induction of General Anesthesia in Geriatric Patients Undergoing Elective Surgery

Led by Tanta University · Updated on 2025-07-01

189

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this observational study, we will assess cFT by Carotid ultrasound and IVC collapsibility index for prediction of hypotension after induction of general anesthesia in geriatric patients undergoing elective surgery.

CONDITIONS

Official Title

Carotid Artery Corrected Flow Time and Inferior Vena Cava Collapsibility Index for Prediction of Hypotension After Induction of General Anesthesia in Geriatric Patients Undergoing Elective Surgery

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 65 years or older
  • American Society of Anaesthesiologists Physical Status I to II
  • Scheduled to receive general anesthesia for elective surgery
  • Fasted for at least 6 to 8 hours before surgery
Not Eligible

You will not qualify if you...

  • Patients who refuse to participate in the study
  • American Society of Anaesthesiologists Physical Status III or IV
  • History of peripheral arterial disease or atherosclerosis
  • Body mass index greater than 30 kg/m2
  • Presence of arrhythmia or cardiomyopathy
  • Chronic obstructive pulmonary disease (COPD)
  • Baseline systolic arterial pressure of 180 mmHg or higher, or less than 90 mmHg
  • Any episode of low oxygen levels or difficult intubation during anesthesia induction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Faculty of medicine, Tanta university

Tanta, El Gharbyia, Egypt, 31111

Actively Recruiting

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Research Team

T

tarek AH Mostafa

CONTACT

S

sameh Ahmed

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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