NCT07139730

Brief Summary

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

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
5mo left

Started Sep 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress63%
Sep 2025Oct 2026

First Submitted

Initial submission to the registry

August 18, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 24, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

August 24, 2025

Status Verified

August 1, 2025

Enrollment Period

1 year

First QC Date

August 18, 2025

Last Update Submit

August 22, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • effect on serum cortisol level 2 minutes after intubation

    baseline

  • effect on serum cortisol level 2 minutes after intubation

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

    baseline

Study Arms (1)

Effect of Nebulized Lignocaine on the stress Response of Endotracheal Intubation in pediatrics unde

EXPERIMENTAL
Drug: Lignocaine 2% concentration solution

Interventions

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

Effect of Nebulized Lignocaine on the stress Response of Endotracheal Intubation in pediatrics unde

Eligibility Criteria

Age1 Year - 9 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Fractures, Stress

Interventions

Lidocaine

Condition Hierarchy (Ancestors)

Fractures, BoneWounds and Injuries

Intervention Hierarchy (Ancestors)

AcetanilidesAnilidesAmidesOrganic ChemicalsAniline CompoundsAmines

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
doctor

Study Record Dates

First Submitted

August 18, 2025

First Posted

August 24, 2025

Study Start

September 1, 2025

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

August 24, 2025

Record last verified: 2025-08