RecruitingNot Applicable

Comparison of Stress Response Evoked by Conventional Versus Videolaryngoscope

Pakistan124 participantsStarted 2026-03-05

Plain-language summary

Impact of using video laryngoscopy versus direct laryngoscopy technique in terms of improved hemodynamics post intubation and time taken for intubation.

Who can participate

Age range

18 Years – 60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * ASA I \& II * Age 18-60 years. * Preoperatively nonhypertensive and hemodynamically stable patients * Patients scheduled for elective procedures not involving airway surgeries * Patients with informed consent * Mallampati score I and II * Interincisor gap \> 3 cms * BMI less than 30 kg/m² Exclusion Criteria * Patient refusal * ASA III, IV \& V * Hemodynamically unstable patients * Patients with Hypertension and Ischemic Heart Disease (whether controlled or uncontrolled) * Airway abnormalities, including congenital airway malformations \& maxillofacial abnormalities * Head, neck or any facial traumas or history of prior head, neck or airway surgeries * Emergency procedures * Pregnancy

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Heart rate

Timeframe: Perioperative

Systolic Blood Pressure

Timeframe: Perioperative

Diastolic Blood Pressure

Timeframe: Perioperative

Mean Blood Pressure

Timeframe: Perioperative

Trial details

NCT IDNCT07510542

SponsorSindh Institute of Urology and Transplantation

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-09-05

Contact for this trial

Syed M Abbas, FCPS

02199215718 smabbas1969@gmail.com

View on ClinicalTrials.gov More Laryngoscopy trials

Who can participate

Age range

18 Years – 60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.