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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04238234
Other study ID # N-68-2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 5, 2021
Est. completion date November 1, 2021

Study information

Verified date October 2021
Source Cairo University
Contact Bassant abdelhamid, M.D.
Phone 01224254012
Email bassantmohamed197@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This thesis aims to evaluate the ability of preoperative plethysmographic variability index to predict post-induction hypotension in comparison with ultrasound measurements of inferior vena cava (IVC) diameter.


Description:

Prospective cohort study. Upon arrival to the operating room, routine monitors (ECG, pulse oximetry, and non-invasive blood pressure monitor) will be applied, intravenous line will be secured and routine premedications (ranitidine 50 mg and ondansteron 4mg) will be administrated. Then inferior vena cava ultrasonography will be performed. Maximum and minimum IVC diameters over a single respiratory cycle will be measured using built-in software. The CI will be calculated as: CI = (dIVCmax - dIVCmin)/dIVCmax , it will be expressed as a percentage. Plethysmographic variability index and a perfusion index readings will be taken preinduction in the form of three readings on one-minute interval. Induction of anaesthesia will be achieved using propofol (2 mg/Kg) and atracurium (0.5 mg/Kg). Endotracheal tube will be inserted after 3 minutes of mask ventilation. Anaesthesia will be maintained by isoflurane (1-1.5%) and atracurium 10 mg increments every 20 minutes. Ringer lactate solution will be infused at a rate of 2 mL/Kg/hour. Any episode of hypotension (defined as mean arterial pressure < 80% of the baseline reading) will be managed by 5mcg norepinephrine.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date November 1, 2021
Est. primary completion date October 30, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Adult patients (>18years) - ASA I-II-III - Patients scheduled for elective surgeries under general anaesthesia. Exclusion Criteria: - Operations which will last for less than 15 minutes. - Patients with cardiac morbidities (impaired contractility with ejection fraction < 40% and tight valvular lesions, unstable angina). - Patients with heart block and arrhythmia (atrial fibrillation and frequent ventricular or supraventricular premature beat). - Patient with decompansted respiratory disease (poor functional capacity, generalized wheezes, peripheral O2 saturation < 90% on room air). - Patients with increased intraabdominal pressure (intrabdominal mass compressing IVC). - Patients with peripheral vascular disease or long standing DM affecting PVI readings. - Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
IVC Ultrasonography
Ultrasound measurements will be performed using a curved transducer set to abdominal mode (1-5 MHz; Acuson x300; Siemens Healthcare, Seoul, Korea). IVC variation will be assessed using ultrasound in the long-axis (sagittal) view. IVC diameter will be measured 1 cm distal to its junction with hepatic vein either by 2-D or M modes via a subcostal approach according to the methodology described by the American Society of Echocardiography . A two-dimensional image of the IVC as it enters the right atrium will be first obtained.
Plethysmographic variability index (PVI) and perfusion index readings (PI)
The PVI and PI will be recorded in the supine position by an anaesthesiologist who was not involved in the further intraoperative monitoring of the patient using Masimo SET ("MightySat 9900, Masimo Corporation, Irvine, CA, USA). PVI (%) is a measure of the dynamic change in PI that occurs during one or more complete respiratory cycles, calculated as: PVI= [(PImax-PImin)/PImax] x100

Locations

Country Name City State
Egypt Almaza Militrary Hospital Cairo
Egypt Kasr alainy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (3)

Tsuchiya M, Yamada T, Asada A. Pleth variability index predicts hypotension during anesthesia induction. Acta Anaesthesiol Scand. 2010 May;54(5):596-602. doi: 10.1111/j.1399-6576.2010.02225.x. Epub 2010 Mar 10. — View Citation

Wesselink EM, Kappen TH, Torn HM, Slooter AJC, van Klei WA. Intraoperative hypotension and the risk of postoperative adverse outcomes: a systematic review. Br J Anaesth. 2018 Oct;121(4):706-721. doi: 10.1016/j.bja.2018.04.036. Epub 2018 Jun 20. — View Citation

Zhang J, Critchley LA. Inferior Vena Cava Ultrasonography before General Anesthesia Can Predict Hypotension after Induction. Anesthesiology. 2016 Mar;124(3):580-9. doi: 10.1097/ALN.0000000000001002. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of the accuracy (Area under receiver operating characteristic curves) of PVI and IVC variation in prediction of post-induction hypotension Maximum and minimum IVC diameters over a single respiratory cycle will be measured using a built-in software.
The CI will be calculated as:
CI = (dIVCmax - dIVCmin)/dIVCmax CI will be expressed as a percentage
10 minutes before general anesthesia
Secondary Plethysmographic variability index (PVI) and a perfusion index readings (PI) Three readings, on one-minute interval before general anesthesia induction 3 minutes
Secondary Maximum and minimum IVC diameters Maximum and minimum IVC diameters over a single respiratory cycle will be measured using built-in software. The CI will be calculated as:
CI = (dIVCmax - dIVCmin)/dIVCmax , it will be expressed as a percentage.
10 minutes
Secondary Mean arterial blood pressure measured at 1-minute intervals starting from the baseline preoperative reading until skin incision as follows: preinduction reading - 1-minute postinduction reading - 2-minute postinduction reading - preintubation reading - one-minute postintubation reading until skin incision 20 minutes
Secondary Heart rate measured at 1-minute intervals starting from the baseline preoperative reading until skin incision as follows: preinduction reading - 1-minute postinduction reading - 2-minute postinduction reading - preintubation reading - one-minute postintubation reading until skin incision 20 minutes
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