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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03653520
Other study ID # ANES001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 28, 2017
Est. completion date November 4, 2017

Study information

Verified date August 2018
Source Avanti Anesthesia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesized that the combination of Valium, Tramadol and Zofran is superior to the substantially more expensive MKO melt in patient satisfaction after cataract surgery.


Description:

The MKO melt is being marketed as an anesthetic medication for cataract surgery that has the advantage that it eliminates the need for an IV in 85% of patients although that number was established anecdotally. This alternative, however, is very cost limiting.The investigators wanted to see if the current regimen (valium only) or a combination similar to the MKO melt (valium + tramadol + zofran) are as good if not better than the MKO melt for anesthesia and how many patients could have indeed gone with an intravenous line (didn't need any extra medications).


Recruitment information / eligibility

Status Completed
Enrollment 651
Est. completion date November 4, 2017
Est. primary completion date November 2, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients scheduled to undergo cataract surgery with Drs. Mayo and Wade at Kirby Glen Surgery Center

Exclusion Criteria:

- Age <18 years

- Patient is not suitable for the medications for reasons such as unsteady gait, cane, wheelchair, severe dementia (unable to consent), terminal illness

- Allergy to a medication in protocol

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Diazepam
5 or 10mg
Tramadol
50mg or 100mg
Ondansetron
1 or two tabs
MKO melt
1 or 2 MKO melts

Locations

Country Name City State
United States Memorial Hermann Kirby Glen Surgery Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Avanti Anesthesia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patient who needed additional IV medication for cataract surgery Patients who require IV medications for self-reported pain or anxiety during surgery. 1 day
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