Evaluation of Non-Invasive Assessment for Post RFAL Procedure Monitoring Using the Nanowear Wearable Multiple Sensor Vest

Nanowear

Status: Enrolling

Conditions: Elective Surgical Procedures

Treatments: Device: Observational Study: No intervention

Study type: Observational

Funder types: Industry

Identifiers

NCT04721405

NWCT20-SS-003

Details and patient eligibility

About

The objective of this study is to evaluate an experience of post-operative monitoring using the Nanowear wearable multiple sensor vest in plastic surgery

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Signed informed consent to participate in the study.
• Female and male subjects, at least 18 years of age at the time of enrolment
• The patient is scheduled to undergo BodyTite and/or FaceTite procedures.
• The patients should be willing to comply with the study procedure and schedule.

Exclusion criteria

• Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body.
• Pregnancy and nursing.
• Subject unwilling or unable to comply with wearing the Nanowear System 12 hours daily for at least 48 hours Up to 7 days
• As per the practitioner's discretion, refrain from treating any condition that might make it unsafe for the patient