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Effect of General Anesthesia Method on Cardiac Risk Patients on Ischemia Modified Markers

A

Ataturk University

Status

Not yet enrolling

Conditions

Anesthesia

Treatments

Procedure: TIVA
Procedure: GENERAL ANESTHESIA

Study type

Interventional

Funder types

Other

Identifiers

NCT05662163
B.30.2.ATA.0.01.00/296

Details and patient eligibility

About

To examine the effects of the general anesthesia method chosen in non-cardiac surgical operations of patients with cardiac risk on the levels of cardiac markers

Full description

To examine the effects of the general anesthesia method chosen in non-cardiac surgical operations of patients with cardiac risk on the levels of cardiac markers like; serum levels of the Creatine Kinase, Creatine Kinase Myocardial Band, high sensitive troponin, heart-type fatty acid-binding protein, ischemia-modified albumin and albumin. And evaluate the effect of anesthesia method on haemodynamic.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being 18 years or older
  • Getting a score of 2 and above according to the Lee cardiac index
  • Having a non-cardiac surgical procedure that will take at least three hours
  • ASA II or III

Exclusion criteria

  • Under 18 years old
  • Those who refused to participate in the study
  • Patients with chronic renal failure
  • Patients with creatinine value ≥ 1.5 mg/dl
  • Surgery that takes less than 3 hours
  • Patients with liver failure
  • Refusing to participate in the study
  • Being allergic to the drugs used

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

GROUP TIVA
Active Comparator group
Description:
Anesthesia will be maintained with propofol (6-10 mg/kg/hour) and remifentanil (0.1-0.3 μg/kg/min). Blood will be taken from the patients at 0, 1 and 4 hours, centrifuged and stored at -80 degrees. From these examples, CK, CKMB, HIGH SENSITIVE TROPONIN, HFABP, IMA AND ALBUMIN will be studied.
Treatment:
Procedure: TIVA
GROUP INHALATION ANESTHESIA
Active Comparator group
Description:
Anesthesia will be maintained with sevoflurane (2 ml/min) 50% oxygen and remifentanil (0.1-0.3 μg/kg/min). Blood will be taken from the patients at 0, 1 and 4 hours, centrifuged and stored at -80 degrees. From these examples, CK, CKMB, HIGH SENSITIVE TROPONIN, HFABP, IMA AND ALBUMIN will be studied.
Treatment:
Procedure: GENERAL ANESTHESIA

Trial contacts and locations

0

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Central trial contact

Canan Atalay; Ayşenur Dostbil

Data sourced from clinicaltrials.gov

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