NCT07504315

Brief Summary

this study aim to compare the effect of different technique of airway managment during anaesthesia on the haemodynamics and intraocular pressure in pediatric patient undergoing congenital glaucoma surgery. Patients were divided into three groups of 25 patients each. (Group A); patients who were subjected to LMA insertion (group B ).

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
75

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

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

First Submitted

Initial submission to the registry

February 25, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

March 10, 2026

Completed
21 days until next milestone

First Posted

Study publicly available on registry

March 31, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Completed
19 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2026

Completed
Last Updated

March 31, 2026

Status Verified

March 1, 2026

Enrollment Period

3 months

First QC Date

February 25, 2026

Last Update Submit

March 25, 2026

Conditions

Keywords

effect of airway management on Intraocular pressure

Outcome Measures

Primary Outcomes (1)

  • intraocular pressure in cm water

    Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation.

Secondary Outcomes (1)

  • blood pressure in form of mmhg and pulse in form of beat per minute

    Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation

Study Arms (3)

. (Group A); patients who were subjected to LMA insertion

ACTIVE COMPARATOR
Device: laryngeal mask insertion

(group B );patients who were subjected to I gel tube insertion

ACTIVE COMPARATOR
Device: I gel mask insertion

and (group C )patients who were subjected to conventional laryngoscopy and endotracheal intubation

ACTIVE COMPARATOR
Device: Endotracheal tube insertion

Interventions

in this intervention air way management in form of laryngeal mask insertion during anesthesia

. (Group A); patients who were subjected to LMA insertion

Air way management in form of I Gel mask insertion during anesthesia

(group B );patients who were subjected to I gel tube insertion

airway management in form of conventional laryngoscopy and endotracheal intubation

and (group C )patients who were subjected to conventional laryngoscopy and endotracheal intubation

Eligibility Criteria

Age2 Months - 10 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • patient ASA grade I-II scheduled to undergoing congenital glaucoma surgery under general anaesthesia

You may not qualify if:

  • the patient with cardiovascular problems. Patients with upper respiratory tract infection. Predicted difficult intubation patients . Full stomach patients. Patients with other congenital anomalies. Patients with previous surgically corrected congenital glaucoma in the measured eye

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hydrophthalmos

Interventions

Intubation, Intratracheal

Condition Hierarchy (Ancestors)

Eye AbnormalitiesEye DiseasesGlaucoma, Open-AngleGlaucomaOcular HypertensionCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesInfant, Newborn, Diseases

Intervention Hierarchy (Ancestors)

Airway ManagementTherapeuticsIntubationInvestigative Techniques

Central Study Contacts

waleed Ahmed, lecturer

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
lecturer of anaesthesia and intensive care

Study Record Dates

First Submitted

February 25, 2026

First Posted

March 31, 2026

Study Start

March 10, 2026

Primary Completion

June 1, 2026

Study Completion

June 20, 2026

Last Updated

March 31, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share