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A Comparison Of The Effect Of Target-Controlled Infusion Anesthesia And Inhalation Anesthesia

T

TC Erciyes University

Status

Completed

Conditions

Cardiology
Pediatric Patients

Treatments

Procedure: TIVA/TCI

Study type

Observational

Funder types

Other

Identifiers

NCT06265610
2022/186

Details and patient eligibility

About

A total of 70 patients who underwent angiographic examination, ASD closure, VSD closure, PDA closure and aortic balloon dilatation were included in this study.

Full description

A total of 70 patients who underwent angiographic examination, ASD closure, VSD closure, PDA closure and aortic balloon dilatation were included in this study. Patients underwent standard electrocardiography (ECG) monitoring with heart rate (HR), noninvasive blood pressure (NIKB), peripheral oxygen saturation (SpO2) and Bispectral index (BIS). Baseline NIKB, SpO2 and HR were recorded before the procedure, intraoperatively and in the postoperative recovery unit. In the postoperative recovery unit, the patient's recovery time was also evaluated and recorded with the Modified Aldrete Recovery Score.

Enrollment

70 patients

Sex

All

Ages

3 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Children weighing over 10 kg and between the ages of 3-18 who will undergo angiography
  2. Patients who are not allergic to the drugs used

Exclusion criteria

  1. ASA Ⅳ patients
  2. Patients with Diabetes Mellitus
  3. Patients with severe lung disease
  4. Patients with psychiatric disorders
  5. Patients with opioid addiction -

Trial design

70 participants in 2 patient groups

group 1
Description:
Total intravenous anesthesia with target-controlled infusion (TCI/TIVA) was applied as an anesthesia method to be applied to patients during cardiology angiography procedures.
Treatment:
Procedure: TIVA/TCI
Group 2
Description:
In the anesthesia method to be applied to patients during cardiology angiography procedures, inhalation anesthesia was applied.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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