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Recruiting NCT07510542

NCT07510542 Comparison of Stress Response Evoked by Conventional Versus Videolaryngoscope

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Clinical Trial Summary
NCT ID NCT07510542
Status Recruiting
Phase
Sponsor Sindh Institute of Urology and Transplantation
Condition Laryngoscopy
Study Type INTERVENTIONAL
Enrollment 124 participants
Start Date 2026-03-05
Primary Completion 2026-09-05

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Endotracheal Intubation through a Video Laryngoscope (VL)Endotracheal Intubation through a Direct Laryngoscope (DL)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 124 participants in total. It began in 2026-03-05 with a primary completion date of 2026-09-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

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

Contact & Investigator

Central Contact

Syed M Abbas, FCPS

✉ smabbas1969@gmail.com

📞 02199215718

Principal Investigator

Syed M Abbas

PRINCIPAL INVESTIGATOR

Sindh Institute of Urology and Transplantation

Frequently Asked Questions

Who can join the NCT07510542 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Laryngoscopy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07510542 currently recruiting?

Yes, NCT07510542 is actively recruiting participants. Contact the research team at smabbas1969@gmail.com for enrollment information.

Where is the NCT07510542 trial being conducted?

This trial is being conducted at Karachi, Pakistan.

Who is sponsoring the NCT07510542 clinical trial?

NCT07510542 is sponsored by Sindh Institute of Urology and Transplantation. The principal investigator is Syed M Abbas at Sindh Institute of Urology and Transplantation. The trial plans to enroll 124 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology