Overview

A Randomized Controlled Trial of Intranasal Dexmedetomidine

Status:
Recruiting
Trial end date:
2023-03-31
Target enrollment:
0
Participant gender:
All
Summary
We designed this study to examine whether the intranasal dexmedetomidine, as a preoperative drug, could improve the satisfaction of adult patients undergoing phacoemulsification cataract surgery.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Guangzhou First People's Hospital
Treatments:
Dexmedetomidine
Criteria
Inclusion Criteria: Cataract patients over 65 years scheduled for elective
phacoemulsification and intraocular lens implantation in Department of Ophthalmology,
Guangzhou First People's Hospital will be recruited in this study. Recruited patients shall
own normal intelligence and understanding capability and their best corrected visual acuity
more than 0.1 in either eye.

Exclusion Criteria: 1) a known allergy or hypersensitivity to dextrometropine or other
anesthetics; 2) a previous history of heart disease; 3) a heart rate (HR) <45 beats per
minute (bpm); 4) a second- or third-degree atrioventricular block; 5) patients on
antihypertensive drugs, such as α-methyldopa, clonidine, or other α2-adrenergic agonists;
6) asthma; 7) sleep apnea syndrome; 8) organ dysfunction; 9) patients with mental illness;
and 10) the long-term use of sedatives and analgesics.

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