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ULTRAPREP Used to Perform Skin Antisepsis Outside the Operating Room

NCT04600310 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2020-10-23

No results posted yet for this study

Summary

Testing ULTRAPREP (consists of a clear bag sealed on one end with the other end enclosing the patients extremity) for safety and efficacy to perform skin antisepsis outside the operating room.

Conditions

  • Time Saved Performing Skin Antisepsis Process Outside the OR
  • Antisepsis of Skin Preparation Outside the OR

Interventions

DEVICE

ULTRAPREP

ULTRAPREP device for reducing OR prep times.

DEVICE

No Intervention

Conventional skin preparation technique

Sponsors & Collaborators

  • Prep Tech, LLC

    lead OTHER

Principal Investigators

  • Pete Prados, Business · PrepTech, LLC

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-04-17
Primary Completion
2019-01-17
Completion
2019-01-17
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04600310 on ClinicalTrials.gov