NCT07300878

Brief Summary

In general anestheisa airway is secured by passing a tube down the widpipe. This helps the patient to breath via ventilator during anesthesia. For placing this tube laryngoscopy is done which results in increase in blood pressure and heart rate. This study will compare the rise in blood pressure and heart rate among when using video laryngoscope with conventional laryngoscope.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
208

participants targeted

Target at P75+ for phase_4

Timeline
1mo left

Started Dec 2025

Shorter than P25 for phase_4

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress75%
Dec 2025Jun 2026

First Submitted

Initial submission to the registry

December 21, 2025

Completed
1 day until next milestone

Study Start

First participant enrolled

December 22, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 24, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 22, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 22, 2026

Last Updated

December 24, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

December 21, 2025

Last Update Submit

December 21, 2025

Conditions

Keywords

Laryngoscopic stress responseVideo laryngoscopyConventional laryngoscopy

Outcome Measures

Primary Outcomes (1)

  • Heart Rate

    Upon arrival in OR (baseline) then immediately following intubation (T1) and then at 3,5,10 minutes following intubation

Secondary Outcomes (3)

  • Mean Blood Pressure

    This will be measured upon arrival in OR (baseline) immediately following intubation(T1) and then at 3,5,10 minutes following intubation

  • Systolic Blood Pressure

    This will be measured upon arrival in OR (baseline) immediately following intubation(T1) and then at 3,5,10 minutes following intubation

  • Diastolic Blood Pressure

    This will be measured upon arrival in OR (baseline) immediately following intubation(T1) and then at 3,5,10 minutes following intubation

Study Arms (2)

Video laryngoscopy

EXPERIMENTAL

Patient in this group will be intubated using hyperangulated C MAC video laryngoscope

Device: C MAC hyperangulated video laryngoscopy

Conventional Laryngoscopy

ACTIVE COMPARATOR

Patient in this group will be intubated using conventional macintosh laryngoscopic blade

Device: Conventional macintosh laryngoscopy

Interventions

Patient in this group will be intubated using conventional macintosh laryngoscopy

Conventional Laryngoscopy

Patient will be intubated using hyperangulated C MAC video laryngoscope

Video laryngoscopy

Eligibility Criteria

Age16 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Elective surgeries under General Endotracheal Anesthesia. ASA class I and II.

You may not qualify if:

  • Pregnancy
  • Body mass index \>35 kg/m2
  • No teeth
  • Maxillofacial trauma
  • Limited Cervical spine movement
  • Upper Airway Tumors
  • Preoperative assessment indicating difficult airway requiring use of video laryngoscope or fiberoptic intubation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Deparment of Anesthesia PIMS

Islamabad, 44000, Pakistan

Location

Related Publications (1)

  • Wang L, Li H, Zhong Y, Ye S, Deng J, Pan T, Zhang Y. Comparative Analysis of Hemodynamic Responses and Oropharyngeal Complications in Tracheal Intubation: Evaluating Conventional, Video, and Rigid Video Laryngoscopes Under General Anesthesia. Med Sci Monit. 2024 Sep 5;30:e944916. doi: 10.12659/MSM.944916.

    PMID: 39233395BACKGROUND

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 21, 2025

First Posted

December 24, 2025

Study Start

December 22, 2025

Primary Completion (Estimated)

June 22, 2026

Study Completion (Estimated)

June 22, 2026

Last Updated

December 24, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

This is due to hospital and ethical committee policies

Locations