Dexmedetomidine and Propofol for Sedation in Cataract Surgery.

Recruiting N/A Interventional Study
Sedation Cataract Hemodynamic Hemodynamic Changes Dexmedetomidine Propofol Dosage Fentanyl Bradycardia Tachycardia Nausea and Vomiting
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
1,000 (estimated)
Sponsor
Saint-Joseph University · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The goal of this prospective, randomized, single-blinded is to learn if there is an ideal sedation protocol in cataract surgery in adults. The main questions it aims to answer are: * Does the combination of Dexmedetomidine and Propofol affect significantly Ramsay sedation scale, compared to Dexmedetomidine and compared to Propofol? * How does each sedation protocol affect hemodynamics? (Heart ra…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Adults undergoing cataract surgery Exclusion Criteria: * Severe hepatic insufficiency * Third degree AV block * Patient refusal
Contacts

Rhea Nacouzi, MD

+961 3359528

rhea.nacouzi@net.usj.edu.lb

CONTACT