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.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 1,000 (estimated)
- Sponsor
- Saint-Joseph University · Other
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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
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Eligibility Criteria
Inclusion Criteria:
* Adults undergoing cataract surgery
Exclusion Criteria:
* Severe hepatic insufficiency
* Third degree AV block
* Patient refusal
Contacts