E-MOHS Trial of TENS and Vibration During Local Anesthesia
NCT: NCT07852455 · NOT_YET_RECRUITING
Brief Summary
The E-MOHS Trial is a randomized controlled trial evaluating whether active vibration plus transcutaneous electrical nerve stimulation reduces pain during local anesthetic infiltration in adults undergoing Mohs micrographic surgery or dermatologic excision. Participants will be randomized to active vibration:TENS or sham TENS during the first local anesthetic administration. The primary outcome is patient-reported infiltration pain during active local anesthetic infiltration, measured using the 11-point Numeric Rating Scale. Secondary outcomes include infiltration pain measured using a Visual Analog Scale, perioperative anxiety, participant satisfaction, willingness to reuse the device, operator-rated ease of use and sterile-field compatibility, blinding integrity, and adverse events.
Frequently Asked Questions
What is E-MOHS Trial of TENS and Vibration During Local Anesthesia?
E-MOHS Trial of TENS and Vibration During Local Anesthesia is a clinical trial registered under NCT07852455. Current status: NOT_YET_RECRUITING.
What is the status of NCT07852455?
The current status of NCT07852455 (E-MOHS Trial of TENS and Vibration During Local Anesthesia) is: NOT_YET_RECRUITING.
When did E-MOHS Trial of TENS and Vibration During Local Anesthesia start?
E-MOHS Trial of TENS and Vibration During Local Anesthesia started on 2027-01-01.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.