Enrolling by invitation NCT07213622

The Use of Smart Glasses for Saphenous Nerve Adductor Canal Block

No phase Interventional Total Knee Arthroplasty

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Smartglasses.
Who it may be relevant to: Registry conditions: Total Knee Arthroplasty. Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: United States
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

The use of smart glasses for saphenous nerve adductor canal blocks compared to standard of care.

Time from needle insertion to complete local anesthetic injection [Time frame: Until the end of the study]

Secondary outcome measures (1)

Number of needle adjustments by user, ergonomics, head adjustments [Time frame: until the end of the study]

Patients with local infection at nerve block site
BMI >40
Patients who are at risk for local anesthesia systemic toxicity due to intraoperative local dose
Patients with nerve damage to the femoral or saphenous nerve
Documented history of mental or cognitive disabilities in EMR
Non-English speaking patient
Pregnant Women (self-reported)
Prisoners
Patients under the age of 18

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

United States · 1 center

NCT: NCT07213622 · STUDY00000465