Study Aim to Compare the Effect of Different Technique of Airway Managment During Anaesthesia on the Haemodynamics and Intraocular Pressure. Patients Were Divided Into Three Groups of 25 Patients Each. (Group A); Patients Who Were Subjected to LMA Insertion (Group B ). (Airway and IOP)

March 25, 2026 updated by: Waleed Adel Ahmed, Sohag University

Different Methods for Airway Management and Their Effect on Intraocular Pressure and Hemodynamics in Pediatrics Undergoing Congenital Glaucoma Surgery

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 ).

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

75

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: . (Group A); patients who were subjected to LMA insertion
Device: laryngeal mask insertion
in this intervention air way management in form of laryngeal mask insertion during anesthesia
Active Comparator: (group B );patients who were subjected to I gel tube insertion
Device: I gel mask insertion
Air way management in form of I Gel mask insertion during anesthesia
Active Comparator: and (group C )patients who were subjected to conventional laryngoscopy and endotracheal intubation
Device: Endotracheal tube insertion
airway management in form of conventional laryngoscopy and endotracheal intubation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
intraocular pressure in cm water
Time Frame: Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation.
Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation.

Secondary Outcome Measures

Outcome Measure
Time Frame
blood pressure in form of mmhg and pulse in form of beat per minute
Time Frame: Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation
Immediately after intubation 2 ,3 , 5 minutes after intubation and 5 minutes after extubation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sohag University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 10, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 20, 2026

Study Registration Dates

First Submitted

February 25, 2026

First Submitted That Met QC Criteria

March 25, 2026

First Posted (Actual)

March 31, 2026

Study Record Updates

Last Update Posted (Actual)

March 31, 2026

Last Update Submitted That Met QC Criteria

March 25, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Soh-med-25-9----IPD

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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