Health TrialsbyHealthPanel

Effect of Nebulized Lignocaine on the Stress Response of Endotracheal Intubation in Pediatrics Undergoing Tonsillectomy Operation Monitored by Rise in Serum Cortisol Level Post Intubation

ConditionStress Response
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-9
SponsorAssiut University

About this trial

This randomized clinical trial aims to is examining the effect of preoperative nebulized lidocaine on the stress response to intubation, monitored by rise in serum cortisol level post intubation

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Elective tonsillectomy operation 2- pediaterics below 9 years old 3- ASA I OR II

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Lignocaine 2% concentration solution

    Drug

    the effect of preoperative nebulized lidocaine on the stress response to intubation, monitored by rise in serum cortisol level post intubation

Treatment groups

70 Participants
are divided into 1 treatment group
Group A: Effect of Nebulized Lignocaine on the stress Response of Endotracheal Intubation in pediatrics undeExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

effect on serum cortisol level 2 minutes after intubation

Time frame
baseline
2

effect on serum cortisol level 2 minutes after intubation

effect on serum cortisol level 2 minutes after intubation to asses decrease in stress response

Time frame
baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assiut University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: