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Remimazolam for Cataract Surgery

About

Brief Summary

The goal of this study is to assess any post operative cognitive changes following benzodiazepine administration during cataract surgery. The investigators will compare effects of Midazolam vs. Remimazolam on cognition at the time of discharge from the post operative care unit and the next day following surgery.

Cognitive changes will be assessed by administration of Montreal Cognitive Assessment (MoCA).

Participants will:

  • Complete MoCA testing prior to surgery
  • Randomize in either Midazolam or study drug Remimazolam
  • Complete MoCA testing after surgery at the time of discharge in the post anesthesia care unit and the next day of surgery at the time of post operative surgical visit.
  • Complete Patient Satisfaction Survey at the time of discharge from the Post Anesthesia Care Unit (PACU)
Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase 2/Phase 3

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
65 Years
Maximum Age
N/A

Inclusion Criteria:

  • Adult patients age > 65 years undergoing first eye cataract surgery under local topical anesthesia at the University of California, Los Angeles (UCLA).
  • Both male and female patients
  • American Society of Anesthesiologists Class 2, 3, and 4.

Exclusion Criteria:

  • Patients who are unable to consent for the study
  • Patients who are unable to cooperate with the cognitive assessment such as patients with significant visual, auditory, language or other impairment.
  • Patients who are unable to understand simple English commands.
  • Patients who do not wish to have benzodiazepine medication during surgery
  • Patients with a history of severe hypersensitivity reaction to dextran 40 or products containing dextran 40.
  • Patients with chronic pain on opiates.
  • Patients with a history of drug, alcohol abuse/dependence.
  • Patients with BMI > 40.
  • Patients with obstructive sleep apnea (moderate to severe).

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Study Stats
Protocol No.
22-001570
Category
Eye/Ocular Disorders
Principal Investigator
ZHUANG FANG
Contact
Stephanie-Dee Sarovich
Location
  • UCLA Westwood
For Providers
NCT No.
NCT05980117
For detailed technical eligibility, visit ClinicalTrials.gov.