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Completed

NCT Number: NCT04725747

Exploring Sedation Types During Cataract 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.

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Key information

Conditions

Age range

55 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Vance Thompson Vision, Sioux Falls, South Dakota, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Subjects who have undergone sedation in the past 90 days.
  • Women who are pregnant or lactating at the time of the study.
  • Subjects who do not wish to or cannot comply with study procedures.
  • Subject with any cognitive impairment (i.e: Alzheimer's, dementia, etc.) that in the opinion of the investigator may confound the study results.
  • Subjects with history of substance abuse.
  • Subjects that are currently taking a prescription pain medication.
  • 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.
  • Subjects that are not willing to abstain from NSAID or steroid eye drops prior to surgery.
  • Subjects with planned use of femtosecond laser, zepto, iris hooks or a malyugin ring during cataract surgery.
  • Subjects with chronic pain rated moderate to severe within the past week.
  • Subjects that have a psychiatric disorder that is currently uncontrolled.
  • Subjects scheduled for same day bilateral or second eye cataract surgery.

Treatment and study plan

Midazolam/Ketamine HCl 3mg-50mg sublingual

Drug

Single sublingual administration of Midazolam/Ketamine HCl 3mg-50mg sublingually prior to surgery

Intravenous Sedatives with or Without Analgesia

Drug

Standard of Care

Other names: IV Sedation

Primary outcomes

  1. Level of Sedation

    Time frame: Duration of surgery

    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.

  2. Level of Pain

    Time frame: Duration of surgery

    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 speculum
    • Upon first incision
    • Upon insertion of phacoemulsification probe
    • Upon Lens insertion
    • Upon 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 OR
    • 10-15 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 OR
    • 10-15 mins after the subject reaches the PACU
  3. Need for Rescue Medication

    Time frame: Duration of surgery

    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.

Secondary outcomes

  1. Eye Movement During Surgery

    Time frame: Duration of surgery

    Eye movement during surgery (evaluated by a masked evaluator by reviewing operative recording).

  2. Clinician's Global Impression

    Time frame: Duration of surgery

    Clinician's impression of patient's sedation during surgery

  3. Patient Satisfaction

    Time frame: 1 day post operatively

    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.

Other outcomes

  1. Blood pressure changes

    Time frame: Duration of surgery

    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.

  2. Heart rate changes

    Time frame: Duration of surgery

    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.

Sponsors and collaborators

Lead sponsor

Vance Thompson Vision

Other

Registry information

Official study title

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

Acronym: MAKER

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jan 27, 2021
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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