Exploring Sedation Types During Cataract Surgery (MAKER)

A Retrospective Study Exploring Midazolam/Ketamine Melt vs IV Sedation in Subjects Undergoing Intraocular Surgery

This study is designed to explore the sedative and analgesic effectiveness of the Midazolam/Ketamine melt compared to IV sedation in subjects undergoing intraocular surgery.

Study Overview

• Status: Completed
• Conditions: Vital Signs
• Intervention / Treatment: Drug: Midazolam/Ketamine HCl 3mg-50mg sublingual; Drug: Intravenous Sedatives with or Without Analgesia

Detailed Description

Cataract surgery today is a highly effective and efficient procedure, with average times for completion ranging around 15 minutes in duration. Patients undergoing cataract surgery are typically given sedatives and often times pain medication (e.g. opioids) just prior to and during the procedure. The overwhelming majority of patients are given these medications via intravenous administration. The insertion of an IV line has been associated with patient complaints of pain and bruising, and can increase the administrative burden on the clinical staff. In addition to the national crisis surrounding opioid abuse, opioids have many negative side effects during cataract surgery such as respiratory depression, dizziness, nausea, and post- operative vomiting.

To reduce the side effects, improve patient satisfaction, and help surgical center flow the Midazolam/Ketamine melt (MK Melt) has been suggested as an alternative to provide sedation and analgesia in subjects undergoing minor outpatient surgery, such as cataract surgery. The addition of ketamine should provide enough analgesia for the mild discomfort reported during cataract surgery. This study is intended to evaluate the MK Melt and its ability to provide an adequate level of both sedation and intraoperative pain control vs an active control.

• Study Type: Observational
• Enrollment (Actual): 1111
• Phase: Phase 4

Contacts and Locations

Study Locations

• United States
  • South Dakota
    • Sioux Falls, South Dakota, United States, 57108
      • Vance Thompson Vision
    • Sioux Falls, South Dakota, United States, 57108
      • Vance Thompson Vision Clinic

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 55 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

• Sampling Method: Non-Probability Sample

Study Population

Subjects requiring cataract removal

Description

Inclusion Criteria:

1. Subjects must be male or female, and between the ages of 55-80 years old.
2. Subjects willing and able to sign the informed consent and capable of committing to the duration of the study.
3. Subjects undergoing uncomplicated stand-alone cataract surgery without planned use of Omidria or intra-operative lidocaine.
4. Subjects that are willing to have an IV placed prior to intraocular surgery
5. Subjects undergoing first eye cataract surgery
6. Subjects that in the opinion of the investigator can tolerate 1 dose of MK 3/50 Melt.

Exclusion Criteria:

1. Subjects who have undergone sedation in the past 90 days.
2. Women who are pregnant or lactating at the time of the study.
3. Subjects who do not wish to or cannot comply with study procedures.
4. Subject with any cognitive impairment (i.e: Alzheimer's, dementia, etc.) that in the opinion of the investigator may confound the study results.
5. Subjects with history of substance abuse.
6. Subjects that are currently taking a prescription pain medication.
7. Subjects that are not willing to abstain from all over-the-counter pain medication with the exception of 500-1000mg acetaminophen for 24 hours prior to surgery.
8. Subjects that are not willing to abstain from NSAID or steroid eye drops prior to surgery.
9. Subjects with planned use of femtosecond laser, zepto, iris hooks or a malyugin ring during cataract surgery.
10. Subjects with chronic pain rated moderate to severe within the past week.
11. Subjects that have a psychiatric disorder that is currently uncontrolled.
12. Subjects scheduled for same day bilateral or second eye cataract surgery.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Cataract Surgery; Individuals undergoing cataract surgical intervention	Drug: Midazolam/Ketamine HCl 3mg-50mg sublingual; Single sublingual administration of Midazolam/Ketamine HCl 3mg-50mg sublingually prior to surgery; Drug: Intravenous Sedatives with or Without Analgesia; Standard of Care; Other Names: IV Sedation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Level of Sedation	The Doctor/Nurse Anesthetist will evaluate the subject's level of sedation on the Ramsey Sedation Scale. Adequate sedation demonstrated by a score of 2 or higher on the Ramsey Scale: Upon entering operative room (before being prepped and draped); Immediately post-op upon entering the PACU The Ramsey scale is: Patient is anxious and agitated or restless, or both; Patient is co-operative, oriented, and tranquil; Patient responds to commands only; Patient exhibits brisk response to light glabellar tap or loud auditory stimulus; Patient exhibits a sluggish response to light glabellar tap or loud auditory stimulus; Patient exhibits no response Source: Ramsay MA, Savege TM, Simpson BR, Goodwin R. Controlled sedation with alphaxolone-alphadalone. BMJ. 1974;2:656-659.	Duration of surgery
Level of Pain	Adequate pain control demonstrated by a score of 3 or below on the Numeric Pain Rating Scale (NPRS) by asking the following questions at the following times: "How painful was that on a scale of 0=no pain to 10=extreme pain?" will be asked:Upon insertion of the speculumUpon first incisionUpon insertion of phacoemulsification probeUpon Lens insertionUpon removal of sterile drape; "How would you rate your worst pain during surgery on a scale of 0=no pain to 10=extreme pain?" will be asked:Immediately after surgery in the OR10-15 mins after the subject reaches the PACU; "On a scale of 0=no pain to 10=extreme pain what number best describes your overall pain during the surgery?" Will be asked:Immediately after surgery in the OR10-15 mins after the subject reaches the PACU	Duration of surgery
Need for Rescue Medication	Percentage of patients requiring rescue medication (IV Fentanyl) for pain. Rescue medication will only be giving if a subject reports a pain level of 4 or higher on the NPRS.	Duration of surgery

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Eye Movement During Surgery	Eye movement during surgery (evaluated by a masked evaluator by reviewing operative recording).	Duration of surgery
Clinician's Global Impression	Clinician's impression of patient's sedation during surgery	Duration of surgery
Patient Satisfaction	Patient satisfactions, determined by asking the patient "How satisfied were you with your overall experience?" at the one-day post-op or via phone call one-day post-op.	1 day post operatively

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Blood pressure changes	Blood pressure will be tracked at 3-5 minute intervals throughout the surgery. Any changes in blood pressure >20mmHg in systolic or diastolic will be identified as a clinically meaningful change.	Duration of surgery
Heart rate changes	Heart rate will be tracked at 3-5 minute intervals throughout the surgery. Any changes in heart rates greater than 100 beats per minute or less than 60 beats per minute will be identified as a clinically meaningful change.	Duration of surgery

Collaborators and Investigators

• Sponsor: Vance Thompson Vision
• Investigators: Principal Investigator: John Berdahl, MD, Vance Thompson Vision Clinic Prof. LLC

Study record dates

Study Major Dates

• Study Start (Actual): January 25, 2021
• Primary Completion (Actual): May 30, 2021
• Study Completion (Actual): June 30, 2021

Study Registration Dates

• First Submitted: January 19, 2021
• First Submitted That Met QC Criteria: January 22, 2021
• First Posted (Actual): January 27, 2021

Study Record Updates

• Last Update Posted (Actual): May 4, 2026
• Last Update Submitted That Met QC Criteria: April 27, 2026
• Last Verified: April 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Organic Chemicals; Heterocyclic Compounds; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Hydrocarbons; Cyclohexanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Anesthesia and Analgesia; Benzazepines; Benzodiazepines; Midazolam; Ketamine; Analgesia
• Other Study ID Numbers: MAKER

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No