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Effect of Carotid Ultrasound-guided Fluid Management on Anesthetic-induced Hypotension in Elderly Patients Undergoing Gastrointestinal Surgery

Not Applicable
Recruiting
Conditions
Hypotension on Induction
Interventions
Other: Fluid therapy under the guide of Carotid ultrasound
Registration Number
NCT05891951
Lead Sponsor
Min Su
Brief Summary

The goal of this clinical trial is to learn about Whether carotid ultrasound guided fluid management can reduce the incidence of hypotension after general anesthesia induction in elderly patients undergoing gastrointestinal surgery.

The main question\[s\] it aims to answer are:

Whether fluid therapy reduces the incidence of general anaesthesia induced hypotension in elderly patients undergoing gastrointestinal surgery.

Whether carotid ultrasound can guide fluid management in elderly patients undergoing gastrointestinal surgery.

Participants will use carotid ultrasound to assess volume status. If volume is insufficient, fluid therapy will be selected until volume is sufficient, anesthesia will be then induced. If volume is sufficient, anesthesia will be directly induced. There is a comparison group: No carotid ultrasound will be used to assess the volume status of the patients, and anesthesia will be directly induced.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Age 60-80 years old
  • gender unlimited
  • ASA: Grade I-Ⅲ
  • BMI:18-30kg/㎡
  • Patients undergoing elective gastrointestinal surgery under general anesthesia Informed consent
Exclusion Criteria
  • Carotid artery stenosis ≥50%
  • Patients with heart valve disease
  • Patients with left ventricular ejection fraction < 50%
  • Patients with cardiac dysfunction (NYHA grade Ⅲ-Ⅳ and/or NTproBNP≥900pg/ml)
  • Patients Combined with renal insufficiency (creatinine ≥178μmol/L, and/or blood urea nitrogen > 9mmol/L)
  • Preoperative systolic blood pressure> 160mmHg or diastolic blood pressure > 100mmHg
  • Refuse to participate in the test
  • Patients participating in other clinical trials

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
B-Carotid ultrasound guided fluid therapyFluid therapy under the guide of Carotid ultrasoundParticipants will use carotid ultrasound to assess volume status. If volume is insufficient, fluid therapy will be selected until volume is sufficient, anesthesia will be then induced. If volume is sufficient, anesthesia will be directly induced.
Primary Outcome Measures
NameTimeMethod
Occurrence of hypotension after anesthesia inductionGeneral anesthesia induction from the beginning to 20 minutes after induction

Hypotension occurred from anesthesia induction to 20 minutes after induction in both groups.

Secondary Outcome Measures
NameTimeMethod
postoperative deliriumWithin 30 days after surgery

Newly diagnosed delirium by the psychiatric department within 30 days after surgery

Postoperative acute kidney injuryWithin 7 days after surgery

Postoperative creatinine increased for a short period of time to more than 0.3mg/dl (26.5μmol/L) or to more than 1.5 times the preoperative creatinine concentration.

postoperative strokeWithin 30 days after surgery

Any newly diagnosed postoperative neurological dysfunction within 30 days after surgery.

Trial Locations

Locations (1)

China,Chongqing The First Affiliated Hospital of Chongqing Medical University

🇨🇳

Chongqing, Chongqing, China

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