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Validity of Perfusion Index to Evaluate the Level of General Anaesthesia in Children.

Validity of Perfusion Index to Evaluate the Level of General Anaesthesia in Children.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03412214
Acronym
PI/AAI
Enrollment
41
Registered
2018-01-26
Start date
2018-03-20
Completion date
2019-08-20
Last updated
2020-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Awareness, Anesthesia

Brief summary

The aim of this study is to evaluate the validity of perfusion index to determine the level of anesthesia in comparison with auditory evoked potential in children undergoing tonsillectomy.

Detailed description

The use of the perfusion index as an added monitoring tool during anesthesia provides the anesthetist with a number of benefits. It is a useful tool to forewarn the clinician of possible light planes of anesthesia, allowing for agent dose adjustment. It is a preexisting technology that is already widely available and used in most urban, regional,and rural centers, in both developed and developing countries, is noninvasive, continuous, and inexpensive. The AEP Monitor/2 (Danmeter A/S, Odense, Denmark), a commercialized system for depth of anesthesia monitoring, extracts the middle latency auditory evoked potentials (MLAEP) from the EEG-signal by using an autoregressive model with an exogenous input adaptive method

Interventions

DEVICEPerfusion index detected by pulse oximeter

Perfusion index detected by pulse oximeter

DEVICEAAI

The AEP Monitor/2 (Danmeter A/S, Odense, Denmark), a commercialized system for depth of anesthesia monitoring, extracts the middle latency auditory evoked potentials (MLAEP) from the EEG-signal by using an autoregressive model with an exogenous input adaptive method.

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 3-12 years * Elective tonsillectomy due to recurrent or chronic tonsillitis

Exclusion criteria

* Cerebral disease * Cardiac disease, * Renal disease, * Pulmonary disease * Hepatic disease.

Design outcomes

Primary

MeasureTime frameDescription
PIIntroperativePerfusion index detected by pulse oximeter
AAI indexIntraoperativeAAI index detected by AEP monitor

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026