Actively Recruiting

Phase Not Applicable
Age: 40Years - 50Years
All Genders
NCT06583811

Remifentanil and Remimazolam to Limit Patient Movement

Led by Egymedicalpedia · Updated on 2024-09-04

70

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

E

Egymedicalpedia

Lead Sponsor

A

Al-Azhar University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Local anesthetics (LA) may be administered by injection (retrobulbar, peribulbar, subconjunctival, lid, or facial block) or by instillation (topical anesthesia), Considerable drawbacks of local anesthesia in these patients include the fact that a few patients can remain comfortable on an operating table for procedures that exceed two or three hours. Sedation may be helpful with LA to decrease the experience of discomfort, movement and anxiety, which may in turn positively influence hemodynamic parameters, patient satisfaction, and overall improve surgical safety. Sedatives used in eye surgeries include benzodiazepines, opioids, alpha-adrenoceptor agonists, and propofol.

CONDITIONS

Official Title

Remifentanil and Remimazolam to Limit Patient Movement

Who Can Participate

Age: 40Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 40 years
  • Both sexes
  • American Society of Anesthesiology (ASA) physical status I-III
  • Undergoing long-eye surgeries under local anesthesia using peribulbar block with an expected surgical time of more than one hour
Not Eligible

You will not qualify if you...

  • Taking aspirin or anticoagulants
  • Allergy to any study medication
  • Drug abuse
  • Uncontrolled hypertension
  • Hyperthyroidism
  • Frequent cough
  • Impaired hearing
  • Severe liver and kidney dysfunction
  • Neurological or psychological disorders
  • Partial or failed block

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Al-Azhar University hospitals

Cairo, Egypt

Actively Recruiting

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Research Team

A

Ahmed M. Elnagar, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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