Actively Recruiting

Phase 4
Age: 20Years - 50Years
All Genders
ID06752863

Comparative Study of Labetalol Versus Dexmedetomidine Infusion in Hypotensive Anesthesia for Ear, Nose, and Throat Surgeries

Led by Ain Shams University · Updated on 2024-12-31

80

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare the effects of Labetalol infusion and Dexmedetomidine infusion in creating hypotensive anesthesia during ear, nose, and throat surgeries. Hypotensive anesthesia involves deliberately lowering blood pressure to improve the surgical field, ease the operation, and reduce surgery time. Labetalol is an anti-hypertensive drug that blocks certain adrenergic receptors, while Dexmedetomidine is a selective alpha2 adrenergic agonist that helps lower blood pressure and heart rate during surgery. The study involves administering either Labetalol or Dexmedetomidine through infusion to patients undergoing ear, nose, and throat surgeries to induce hypotension. Both drugs will be evaluated for their ability to maintain controlled low blood pressure during the procedure. The comparison focuses on their roles in hypotensive anesthesia to determine their effectiveness and safety profiles. Participants will be monitored for changes in mean arterial blood pressure before anesthesia induction and every 15 minutes during the hypotensive anesthesia. The study tracks blood pressure over 12 months to assess the drugs' effects throughout the surgical period. Safety and tolerability will be observed, and patient responses to each drug infusion will be carefully recorded to inform outcomes.

CONDITIONS

Official Title

Labetalol Infusion and Dexmedetomidine Infusion in Hypotensive Anesthesia

Who Can Participate

Age: 20Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients classified as American Society of Anesthesiologists I or II who are candidates for ear, nose, and throat surgeries
  • Age between 20 and 50 years
Not Eligible

You will not qualify if you...

  • Patients with uncontrolled hypertension, any degree of heart block, congestive heart failure, bleeding disorders, cerebral insufficiency, liver or kidney problems
  • Patients currently using beta blockers or clonidine
  • Pregnant or breastfeeding women
  • Patients allergic to any anesthetic or hypotensive drugs used in the study
  • Patients who do not agree to participate in the trial

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ain Shams university

Cairo, Cairo Governorate, Egypt, 11517

Actively Recruiting

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Research Team

N

Nourhan Osama, Master degree

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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